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| aid | Article Title | Organization | Deposition |
|---|---|---|---|
| aid1159522 | Identify HuR specific inhibitors | University of Texas Health Science Center | 11/09/16 |
| aid1224863 | Phenotypic Assay to Identify Small Molecules that Upregulate Production of hCFTR in HeLa Cells | Southern Research Institute | 11/09/16 |
| aid1224899 | mTOR Inhibition with eCF309 | Innovative Therapeutics Lab | 11/09/16 |
| aid1117296 | Counterscreen for activators of Transthyretin (TTR) transcription: Luminescence-based cell-based high throughput dose response assay to identify inhibitors of Transthyretin (TTR) transcription in HuH7 hepatoma cells | The Scripps Research Institute Molecular Screening Center | 01/12/15 |
| aid1117295 | Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Trypanosoma brucei RNA editing ligase 1 (TbREL1). | The Scripps Research Institute Molecular Screening Center | 01/12/15 |
| aid1117297 | Luminescence-based cell-based high throughput dose response assay to identify activators of Transthyretin (TTR) transcription | The Scripps Research Institute Molecular Screening Center | 01/12/15 |
| aid1053171 | Counterscreen for inhibitors of LEDGF/p75-dependent integration: TR-FRET-based biochemical high throughput dose response counterscreen assay to identify activators of HIV-1 Integrase multimerization | The Scripps Research Institute Molecular Screening Center | 08/09/14 |
| aid1053172 | TR-FRET-based biochemical high throughput dose response assay to identify inhibitors of HIV-1 LEDGF/p75 DNA Integration | The Scripps Research Institute Molecular Screening Center | 08/09/14 |
| aid743037 | Counterscreen for agonists of the daf-12 abnormal Dauer Formation: Luminescence-based cell-based dose response assay to identify agonists of the Liver-X-Receptor (LXR). | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743052 | Counterscreen for agonists of the daf-12 abnormal Dauer Formation: Luminescence-based cell-based dose response screening assay to identify agonists of the Liver-X-Receptor (LXR) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720737 | Counterscreen for agonists of the daf-12 abnormal Dauer Formation: Luminescence-based cell-based screening assay to identify agonists of the Liver-X-Receptor (LXR). | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743253 | Counterscreen for exosite inhibitors of ADAM10: QFRET-based biochemical high throughput dose response assay to identify inhibitors of ADAM17 | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743259 | Counterscreen for exosite inhibitors of ADAM17: Fluorescence resonance energy transfer (FRET)-based biochemical high throughput dose response assay to identify inhibitors of ADAM10 | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720547 | Counterscreen for inhibitors of COUP-TFII (NR2F2): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Herpes Virus Virion Protein 16 (VP16) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743329 | Counterscreen for inhibitors of phospholipase C isozymes (PLC-B3): Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of phospholipase C isozymes (PLC-gamma1) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720701 | Dose Response confirmation of small molecule inhibitors originally identified via uHTS of Artemis endonuclease activity via a fluorescence intensity assay | Burnham Center for Chemical Genomics | 08/08/14 |
| aid743297 | Epi Absorbance-based biochemical high throughput dose response assay to identify inhibitors of human tyrosyl-DNA phosphodiesterase 2 (TDP2) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720729 | Fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn6) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720730 | Fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors that disrupt the binding of a cyclic peptide (Tn7) to the fibrin proteolytic product D-Dimer and fragment E complex [DD(E )] | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743328 | Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of phospholipase C isozymes (PLC-B3) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720638 | Late stage Counterscreen for the probe development effort to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A): Luminescence-based cell-based high throughput dose response assay to identify agonists of the mu 1 opioid receptor (OPRM1) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720639 | Late stage for the probe development effort to identify agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A): Luminescence-based cell-based high throughput dose response assay for agonists of the mouse 5-hydroxytryptamine (serotonin) receptor 2A (HTR2A) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720734 | Luminescence-based cell-based high throughput dose response assay to identify activators of the DAF-12 from the parasite S. stercoralis (ssDAF-12) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743038 | Luminescence-based cell-based high throughput dose response assay to identify agonists of the DAF-12 from the parasite H. contortus (hcDAF-12) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743254 | QFRET-based biochemical high throughput dose response assay to identify exosite inhibitors of ADAM10. | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743260 | QFRET-based biochemical high throughput dose response assay to identify exosite inhibitors of ADAM17 | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743457 | QFRET-based biochemical high throughput dose response assay to identify inhibitors of human group III secreted phospholipase A2 enzyme (HGIII-sPLA2) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720645 | TRFRET-based biochemical high throughput dose response assay to identify inhibitors of 5-meCpG-binding domain protein 2 (MBD2)-DBD binding to methylated oligonucleotide | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid743453 | TRFRET-based cell-based high throughput dose response assay to identify inhibitors of cell surface Prion Protein (PRPC) | The Scripps Research Institute Molecular Screening Center | 08/08/14 |
| aid720500 | Fluorescence Intensity-based biochemical primary high throughput dose response assay to identify activators of kallikrein-7 (K7) zymogen | The Scripps Research Institute Molecular Screening Center | 09/18/13 |
| aid720521 | Late stage assay provider counterscreen for TLR9 inhibitors: Luminescence-based assay to identify inhibitors of TLR9-dependent cell activation using RAW264.7 cells | The Scripps Research Institute Molecular Screening Center | 09/18/13 |
| aid720548 | Luminescence-based cell-based high throughput dose response assay to identify inhibitors of COUP-TFII (NR2F2) | The Scripps Research Institute Molecular Screening Center | 09/18/13 |
| aid652151 | Absorbance-based bacterial cell-based high throughput dose response assay to identify inhibitors of RecBCD | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid651967 | Absorbance-based biochemical high throughput dose response assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid652102 | Confirmatory FRET assay using full length substrates for Botulinum neurotoxin light chain A protease, with Powder Set01 | NMMLSC | 06/21/13 |
| aid686983 | Counterscreen for agonists of the human trace amine associated receptor 1 (TAAR1): Fluorescence-based cell-based high throughput dose response assay to identify nonselective Ga16 agonists | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686988 | Counterscreen for agonists of the human trace amine associated receptor 1 (TAAR1): Fluorescence-based cell-based high throughput dose response assay to identify nonselective Ga16 antagonists | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686984 | Counterscreen for agonists of the human trace amine associated receptor 1 (hTAAR1): Fluorescence-based cell-based high throughput dose response assay to identify hTAAR1 agonist that also desensitize TAAR1 receptor response. | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686989 | Counterscreen for antagonists of the human trace amine associated receptor 1 (TAAR1): Fluorescence-based cell-based high throughput dose reponse assay to identify nonselective Ga16 agonists | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686986 | Counterscreen for antagonists of the human trace amine associated receptor 1 (hTAAR1): Fluorescence-based cell-based high throughput dose response assay to identify TAAR1 Agonists | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686987 | Counterscreen for antagonists of the human trace amine associated receptor 1 (hTAAR1): Fluorescence-based cell-based high throughput dose response assay to identify nonselective Ga16 antagonists | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686958 | Counterscreen for inhibitors of T-cell receptor (TCR)-CD3 interaction: Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled BSA probe | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid687018 | Counterscreen for inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1): Luminescence-based cell-based high throughput dose response assay for nonselective inhibitors/assay artifacts using AP2 mutant SF-1 (NR5A1) Transactivation Assay | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid651973 | Counterscreen for inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Herpes Virus Virion Protein 16 (VP16) | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid652002 | Dose Response confirmation of uHTS hits for a small molecule Caspase-8 TRAIL sensitizers in a luminescence panel assay | Burnham Center for Chemical Genomics | 06/21/13 |
| aid652006 | Dose response confirmation of small molecule inhibitors of Low Molecular Weight Protein Tyrosine Phosphatase, LMPTP, in a fluorescence-based, Lymphoid Phosphatase (PTPN22, LYP-1) selectivity Assay | Burnham Center for Chemical Genomics | 06/21/13 |
| aid652005 | Dose response confirmation of small molecule inhibitors of Low Molecular Weight Protein Tyrosine Phosphatase, LMPTP, in an orthogonal absorbance-based assay | Burnham Center for Chemical Genomics | 06/21/13 |
| aid652135 | Fluorescence-based biochemical high throughput dose response assay for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberculosis | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686959 | Fluorescence-based biochemical high throughput dose response assay to identify molecules that bind r(CAG) RNA repeats | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686957 | Fluorescence-based biochemical primary high throughput dose response assay to identify inhibitors of T-cell receptor (TCR)-CD3 interaction using a TAMRA-labeled TCR probe | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686985 | Fluorescence-based cell-based high throughput dose response assay to identify agonists of the human trace amine associated receptor 1 (TAAR1) | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686994 | Fluorescence-based cell-based high throughput dose response assay to identify antagonists of the human trace amine associated receptor 1 (TAAR1) | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid687013 | Fluorescence-based cell-based primary high throughput dose response assay to identify antagonists of the Galanin Receptor 3 (GalR3). | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid651971 | Luminescence-based biochemical high throughput dose response assay for inhibitors of Trypanosoma brucei methionyl tRNA synthetase (MetRS) | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid687017 | Luminescence-based cell-based high throughput dose response assay for inhibitors of the orphan nuclear receptor subfamily 0, group B, member 1 (DAX1; NR0B1): repression of SF-1 (NR5A1) activated StAR promoter by full-length DAX-1 | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid651970 | Luminescence-based cell-based high throughput dose response assay for inverse agonists of the liver receptor homolog-1 (LRH-1; NR5A2) | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686991 | Luminescence-based cell-based high throughput dose response assay to identify activators of the function of SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 (SMARCA2, BRM) | The Scripps Research Institute Molecular Screening Center | 06/21/13 |
| aid686977 | Vibrio cholerae assay for pro-quorum sensing small molecules | Southern Research Specialized Biocontainment Screening Center | 06/21/13 |
| aid651728 | Counter screen for HTS for Beta-2AR agonists with FAP-tagged human CCR5 with Powderset2 | NMMLSC | 06/20/13 |
| aid651937 | Counterscreen for discovery of small molecules that bind to the HIV-1-gp120 binding antibody, PG9 | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651939 | Counterscreen for discovery of small molecules that bind to the HIV-1-gp120 binding antibody, PG9 | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651552 | Counterscreen for inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and receptor-interacting serine-threonine kinase 2 (RIPK2) | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651672 | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651720 | Counterscreen for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5): Luminescence-based biochemical high throughput dose response assay to identify inhibitors of Hepatocyte nuclear factor 4 (HNF4) dimerization | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651579 | Dose Response Confirmation of SKN-1 Inhibitor hits via a heat-shock counterscreen assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651650 | Dose Response confirmation of small molecule modulators of the interaction between CendR and NRP-1 in a panel assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651639 | Dose Response confirmation of uHTS hits for small molecule antagonists of the CRF-binding protein and CRF-R2 receptor complex in 384 well format | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651594 | Dose Response counterscreen of small molecule antagonists of the CXCR6 receptor using a CXCR5 receptor luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651563 | Dose ResponseConfirmation of SKN-1 Inhibitor hits in a fluorescence ratio assay - Set 2 | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651684 | Dose response confirmation of small molecule activators of alpha dystroglycan glycosylation | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651700 | Dose response confirmation of small molecule inhibitors of Low Molecular Weight Protein Tyrosine Phosphatase, LMPTP, via a fluorescence intensity assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651693 | Dose response confirmation of small molecule inhibitors of the catalytic domain of the SUMO protease, SENP1 in a FRET assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651697 | Dose response confirmation of small molecule inhibitors of the catalytic domain of the SUMO protease, SENP1 in a kinetic FRET assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651581 | Dose response confirmation of uHTS identification of HIF-2a Inhibitors in a luminesence assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651709 | Dose response confirmation of uHTS inhibitor hits from NadD in a Colorimetric assay - Set 2 | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651570 | Dose response validation of uHTS Gli-SUFU antagonist hits in a Wnt3a luminescent reporter assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651756 | Dose responses of compounds that inhibit the Choline Transporter (CHT) in a 3H-choline uptake radioactive assay | Johns Hopkins Ion Channel Center | 06/20/13 |
| aid651565 | Dose-response confirmation of uHTS inhibitor hits of Sentrin-Specific Protease 8 in a Caspase-3 Fluorescence assay | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651559 | Dose-response confirmation of uHTS inhibitor hits of Sentrin-Specific Protease 8 using a kinetic assay with Nedd8 Protein Substrate | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651680 | Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 (ASAP1) | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651763 | Fluorescence polarization-based biochemical high throughput dose response screening assay to identify inhibitors of ADP-ribosylation factor GTPase activating protein 1 (ARFGAP1) | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651553 | Fluorescence-based cell-based high throughput dose response assay for inhibitors of the interaction of nucleotide-binding oligomerization domain containing 2 (NOD2) and the receptor-interacting serine-threonine kinase 2 (RIPK2) | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651677 | Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651733 | Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) produced in HEK293T cells | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid651675 | SAR analysis of small molecule activators of alpha dystroglycan glycosylation | Burnham Center for Chemical Genomics | 06/20/13 |
| aid651848 | TRFRET-based biochemical high throughput dose response assay for small molecules that bind to the HIV-1-gp120 binding antibody, PG9 | The Scripps Research Institute Molecular Screening Center | 06/20/13 |
| aid624241 | Dose Response selectivity of inhibitors of STriatal-Enriched Phosphatase (STEP) in the Lymphoid Phosphatase (PTPN22) Inhibition Assay | Burnham Center for Chemical Genomics | 06/25/12 |
| aid624207 | Dose response orthogonal assay of uHTS small molecule inhibitors of Striatal-Enriched Phosphatase via a colorimetric intensity assay. | Burnham Center for Chemical Genomics | 06/25/12 |
| aid624243 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, compounds from Powder Set 01 | NMMLSC | 06/25/12 |
| aid624245 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, compounds from Powder Set 01 | NMMLSC | 06/25/12 |
| aid624244 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Lethal Factor protease, compounds from Powder Set 01 | NMMLSC | 06/25/12 |
| aid623963 | Absorbance-based biochemical high throughput dose response assay for activators of Methionine sulfoxide reductase A (MsrA) | The Scripps Research Institute Molecular Screening Center | 06/19/12 |
| aid602264 | Counterscreen for biased ligands (agonists) of the melanocortin 4 receptor (MC4R): Luminescence-based cell-based high throughput dose response assay to identify agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors | The Scripps Research Institute Molecular Screening Center | 06/19/12 |
| aid602234 | Counterscreen for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3) | The Scripps Research Institute Molecular Screening Center | 06/19/12 |
| aid623996 | Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr1 with Cherry Pick2 compound set | NMMLSC | 06/19/12 |
| aid623994 | Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr2 with Cherry Pick2 compound set | NMMLSC | 06/19/12 |
| aid623992 | Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Mdr1 with Cherry Pick2 compound set | NMMLSC | 06/19/12 |
| aid602473 | Dose Response confirmation of uHTS hits for small molecule agonists of the CRF-binding protein and CRF-R2 receptor complex | Burnham Center for Chemical Genomics | 06/19/12 |
| aid623955 | Dose Response of Flow Cytometric HTS Screen for inhibitors of the ABC transporter ABCB6 for Cherry Pick01 | NMMLSC | 06/19/12 |
| aid602257 | Dose Response of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin, Powder Set1 | NMMLSC | 06/19/12 |
| aid602374 | Dose Response selectivity of inhibitors of STriatal-Enriched Phosphatase (STEP) in the dual-specificity protein-tyrosine phosphatase VHR Inhibition Assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602367 | Dose Response selectivity of inhibitors of Striatal-Enriched Phosphatase (STEP) in a SHP2 (PTPN11) Inhibition Assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602369 | Dose Response validation of uHTS RPN11 inhibitor hits using a Thrombin Fluorescence Polarization assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602304 | Dose Response with BCECF Assay for V-ATPase inhibitors that increase vacuolar pH, Powder Set 1 | NMMLSC | 06/19/12 |
| aid602386 | Dose response confirmation of DNMT1 inhibitors in a Fluorescent Molecular Beacon assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602368 | Dose response confirmation of uHTS RPN11 inhibitor hits in a Fluorescence Polarization assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602464 | Dose response confirmation of uHTS antagonist hits from Gli-SUFU in a luminescent reporter assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602372 | Dose response confirmation of uHTS small molecule inhibitors of Striatal-Enriched Phosphatase via a fluorescence intensity assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid623882 | Dose response for HTS for Beta-2AR agonists via FAP method from Powderset2 | NMMLSC | 06/19/12 |
| aid623947 | Dose response for HTS for Beta-2AR agonists via FAP method from Powderset3 | NMMLSC | 06/19/12 |
| aid602376 | Dose responses of compounds that activate the Choline Transporter (CHT) - 10 point CRC | Johns Hopkins Ion Channel Center | 06/19/12 |
| aid602259 | Dose-response confirmation of microRNA-mediated mRNA deadenylation inhibitors by fluoresence polarization assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602260 | Dose-response secondary confirmation of microRNA-mediated mRNA deadenylation inhibitors by fluoresence polarization assay using Cy5 labeled peptide | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602328 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, compounds from Cherry Pick 02 | NMMLSC | 06/19/12 |
| aid602338 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, compounds from Cherry Pick 02 | NMMLSC | 06/19/12 |
| aid602326 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Lethal Factor protease, compounds from Cherry Pick 02 | NMMLSC | 06/19/12 |
| aid602263 | Luminescence-based cell-based high throughput dose response assay for biased ligands (agonists) of the melanocortin 4 receptor (MC4R) | The Scripps Research Institute Molecular Screening Center | 06/19/12 |
| aid602235 | Luminescence-based cell-based high throughput dose response assay for inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) | The Scripps Research Institute Molecular Screening Center | 06/19/12 |
| aid602469 | SAR analysis of small molecule Activators of Apaf-1 in a Fluorescent assay - set 2 | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602460 | SAR analysis of small molecule Inhibitors of Apaf-1 in a Fluorescent assay - set 2 | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602471 | SAR analysis of small molecule activators of Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay - Set 2 | Burnham Center for Chemical Genomics | 06/19/12 |
| aid624089 | SAR analysis of small molecule inhibitors of APOBEC3A DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 | Burnham Center for Chemical Genomics | 06/19/12 |
| aid624087 | SAR analysis of small molecule inhibitors of APOBEC3G DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay - Set 2 | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602461 | SAR analysis of small molecule inhibitors of Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay - Set 2 | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602375 | SAR analysis of small molecule inhibitors of tim23-1 yeast via a luminescent assay | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602380 | SAR analysis of small molecule inhibitors of tim23-1: a luminescent TIM10 yeast counterscreen. | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602378 | SAR analysis of small molecule inhibitors of tim23-1: a luminescent tim10-1 yeast counterscreen. | Burnham Center for Chemical Genomics | 06/19/12 |
| aid602298 | TRFRET-based cell-based high throughput dose response assay for biased ligands (antagonists) of the melanocortin 4 receptor (MC4R) | The Scripps Research Institute Molecular Screening Center | 06/19/12 |
| aid602151 | Cellular PLD1 concentration response | Vanderbilt Specialized Chemistry Center | 06/18/12 |
| aid602147 | Cellular PLD2 concentration response | Vanderbilt Specialized Chemistry Center | 06/18/12 |
| aid602167 | Counterscreen for inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Herpes Virus Virion Protein 16 (VP16) | The Scripps Research Institute Molecular Screening Center | 06/18/12 |
| aid602168 | Counterscreen for inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3): Luminescence-based cell-based high throughput dose response assay to identify inhibitors of the Steroid Receptor Coactivator 1 (SRC1; NCOA1) | The Scripps Research Institute Molecular Screening Center | 06/18/12 |
| aid602198 | Dose Response of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin, Cherry Pick 2 | NMMLSC | 06/18/12 |
| aid602176 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, compounds from Cherry Pick 01 | NMMLSC | 06/18/12 |
| aid602177 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, compounds from Cherry Pick 01 | NMMLSC | 06/18/12 |
| aid602178 | High-throughput multiplex microsphere dose response for inhibitors of toxin protease, specifically Lethal Factor protease, compounds from Cherry Pick 01 | NMMLSC | 06/18/12 |
| aid602208 | JHICC_CHT_Inh_3H uptake_CRC | Johns Hopkins Ion Channel Center | 06/18/12 |
| aid602166 | Luminescence-based cell-based high throughput dose response assay for inhibitors of the Steroid Receptor Coactivator 3 (SRC3; NCOA3) | The Scripps Research Institute Molecular Screening Center | 06/18/12 |
| aid602150 | PLD1 purified enzyme concentration response | Vanderbilt Specialized Chemistry Center | 06/18/12 |
| aid602149 | PLD2 purified enzyme concentration response | Vanderbilt Specialized Chemistry Center | 06/18/12 |
| aid602136 | SAR analysis of small molecule inhibitors of APOBEC3G DNA Deaminase via a fluorescence-based single-stranded DNA deaminase assay | Burnham Center for Chemical Genomics | 06/18/12 |
| aid602181 | TRFRET-based biochemical high throughput dose response assay for inhibitors of the interaction of the Ras and Rab interactor 1 protein (Rin1) and the c-abl oncogene 1, non-receptor tyrosine kinase (Abl) | The Scripps Research Institute Molecular Screening Center | 06/18/12 |
| aid588783 | Dose Response Assay for Inhibitors of the beta-Arrestin-Adaptor Protein 2 Interaction for Cherry Pick 1 | NMMLSC | 01/06/12 |
| aid588606 | Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr1 with Hit compounds from Cherry Pick1 | NMMLSC | 01/06/12 |
| aid588604 | Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Cdr2 with Hit compounds from Cherry Pick1 | NMMLSC | 01/06/12 |
| aid588608 | Dose Response HTS singleplex for inhibitors of yeast efflux pump, specifically Mdr1 with Hit compounds from Cherry Pick1 | NMMLSC | 01/06/12 |
| aid588554 | Dose Response confirmation of uHTS Activators of the Apaf-1 Pathway in Fluorescent format | Burnham Center for Chemical Genomics | 01/06/12 |
| aid588596 | Dose Response of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin, Cherry Pick 1 | NMMLSC | 01/06/12 |
| aid588592 | Dose Response validation of Activators of Apaf-1 using a Fluorescent Interference Counterscreen assay | Burnham Center for Chemical Genomics | 01/06/12 |
| aid588637 | Dose response assay for compounds that inhibit KCNQ2 potassium channels on automated electrophysiological assay II | Johns Hopkins Ion Channel Center | 01/06/12 |
| aid588584 | Dose response confirmation of the uHTS fluorescent assay for identification of inhibitors of ATG4B Set 2 | Burnham Center for Chemical Genomics | 01/06/12 |
| aid588574 | Dose response confirmation of uHTS hits for Apaf-1 using a LZ-Caspase-9/Caspase-3 Fluorescent Selectivity assay | Burnham Center for Chemical Genomics | 01/06/12 |
| aid588586 | Dose response counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay Set 2 | Burnham Center for Chemical Genomics | 01/06/12 |
| aid588763 | Dose response for HTS for Beta-2AR agonists via FAP method from CP1 | NMMLSC | 01/06/12 |
| aid588775 | Dose response for HTS for Beta-2AR agonists via FAP method from Powderset1 | NMMLSC | 01/06/12 |
| aid588769 | Late stage assay provider results from the probe development effort to identify inhibitors of plasma platelet activating factor acetylhydrolase (pPAFAH): fluorescence-based dose response biochemical gel-based competitive Activity-Based Protein Profiling (ABPP) assay for HTS compounds | The Scripps Research Institute Molecular Screening Center | 01/06/12 |
| aid588601 | SAR Analysis of small molecule inhibitors of Sentrin-specific protease 8 (SENP8) using a Luminescent assay - Set 2 | Burnham Center for Chemical Genomics | 01/06/12 |
| aid588603 | SAR analysis of small molecule activators of the MazEF TA System via a fluorescence-based single-stranded RNase assay | Burnham Center for Chemical Genomics | 01/06/12 |
| aid588411 | Counterscreen for agonists of heterodimerization of the mu 1 (OPRM1) and delta 1 (OPRD1) opioid receptors: Luminescence-based cell-based high throughput dose response assay to identify agonists of OPRD1 homodimerization | The Scripps Research Institute Molecular Screening Center | 01/05/12 |
| aid588538 | Dose Response validation of Inhibitors of Apaf-1 using a Fluorescent Interference Counterscreen assay | Burnham Center for Chemical Genomics | 01/05/12 |
| aid588524 | Dose response confirmation of uHTS hits for Apaf-1 in a Fluorescent assay | Burnham Center for Chemical Genomics | 01/05/12 |
| aid588481 | Dose response confirmation uHTS hits for MazEF TA System activators via a fluorescence-based single-stranded RNase assay | Burnham Center for Chemical Genomics | 01/05/12 |
| aid588502 | Dose response confirmation uHTS hits for MazEF TA System activators via a fluorescence-based single-stranded RNase assay counterscreen | Burnham Center for Chemical Genomics | 01/05/12 |
| aid588400 | Dose response counterscreen of uHTS hits for ATG4B inhibitors in a Phospholipase A2 assay | Burnham Center for Chemical Genomics | 01/05/12 |
| aid588504 | Luminescence-based cell-based high throughput dose response assay for activators of the GAA850 frataxin (FXN) promoter | The Scripps Research Institute Molecular Screening Center | 01/05/12 |
| aid588359 | SAR analysis counterscreen of small molecule antagonists of the CCR6 receptor using an APJ receptor luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 01/05/12 |
| aid588341 | Counterscreen for inhibitors of TLR9-MyD88 binding: fluorescence-based cell-based high throughput dose response assay to identify non-selective inhibitors of the beta-lactamase enzyme (BLA) | The Scripps Research Institute Molecular Screening Center | 01/04/12 |
| aid540297 | Dose Response confirmation of uHTS hits for Scp-1 phosphatase using a colorimetric assay | Burnham Center for Chemical Genomics | 01/04/12 |
| aid540252 | Dose Response orthogonal assay utilizing the direct end-point detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase | Burnham Center for Chemical Genomics | 01/04/12 |
| aid540269 | Dose Response orthogonal kinetic assay utilizing the direct detection of NADPH for uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase | Burnham Center for Chemical Genomics | 01/04/12 |
| aid588340 | Fluorescence-based cell-based high throughput dose response assay for inhibitors of TLR9-MyD88 binding | The Scripps Research Institute Molecular Screening Center | 01/04/12 |
| aid540288 | SAR VHR1 Fluorescent Assay for In Vitro dose response studies Set 3 | Burnham Center for Chemical Genomics | 01/04/12 |
| aid540334 | SAR analysis of small molecule antagonists of the CCR6 receptor: a luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 01/04/12 |
| aid504893 | Counterscreen for activators of the Protein Kinase A-R1A (PKA-R1A) complex: fluorescence polarization-based biochemical high throughput dose response assay to identify activators of the Protein Kinase A-R2B (PKA-R2B) complex | The Scripps Research Institute Molecular Screening Center | 08/04/11 |
| aid504896 | Counterscreen for activators of the Protein Kinase A-R2B (PKA-R2B) complex: fluorescence polarization-based biochemical high throughput dose response assay to identify activators of the Protein Kinase A-R1A (PKA-R1A) complex | The Scripps Research Institute Molecular Screening Center | 08/04/11 |
| aid504762 | Dose Response confirmation of activators of hexokinase domain containing I (HKDC1) in the hexokinase 1 selectivity assay | Burnham Center for Chemical Genomics | 08/04/11 |
| aid504763 | Dose Response confirmation of inhibitors of hexokinase domain containing I (HKDC1) in the hexokinase 1 selectivity assay | Burnham Center for Chemical Genomics | 08/04/11 |
| aid504765 | Dose Response confirmation of uHTS small molecule inhibitors of Plasmodium falciparum Glucose-6-phosphate dehydrogenase via a fluorescence intensity assay | Burnham Center for Chemical Genomics | 08/04/11 |
| aid504887 | Fluorescence polarization-based biochemical high throughput dose response assay for activators of the Protein Kinase A-R1A (PKA-R1A) complex | The Scripps Research Institute Molecular Screening Center | 08/04/11 |
| aid504888 | Fluorescence polarization-based biochemical high throughput dose response assay for activators of the Protein Kinase A-R2B (PKA-R2B) complex | The Scripps Research Institute Molecular Screening Center | 08/04/11 |
| aid504792 | Human Glucose-6-Phosphate Dehydrogenase Dose Response Selectivity Assay for Inhibitors of Plasmodium falciparum Glucose-6-Phosphate Dehydrogenase | Burnham Center for Chemical Genomics | 08/04/11 |
| aid504723 | Dose Response confirmation of APOBEC3A DNA Deaminase Inhibitors via a A3G counterscreen | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504722 | Dose Response confirmation of APOBEC3G DNA Deaminase Inhibitors via a A3A counterscreen | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504549 | Dose Response confirmation of Image-Based HTS for Selective Agonists for NTR1 | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504593 | Dose Response confirmation of Inhibitors of Mdm2/MdmX interaction in luminescent format | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504669 | Dose Response confirmation of Inhibitors of Mdm2/MdmX interaction using a Brca1/Bard1 BiLC Counterscreen assay | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504689 | Dose Response confirmation of UBC13 Polyubiquitin Inhibitors using a Bfl-1 counterscreen | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504730 | Dose Response confirmation of activators of hexokinase domain containing I (HKDC1) | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504729 | Dose Response confirmation of inhibitors of hexokinase domain containing I (HKDC1) | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504724 | Dose Response confirmation of small molecule APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504719 | Dose Response confirmation of small molecule APOBEC3G DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504728 | Dose Response confirmation of small molecule antagonists of the CCR6 receptor: a luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504544 | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1: a luminescent tim23-1 yeast counterscreen. | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504672 | Dose Response confirmation of uHTS small molecule inhibitors of tim23-1: a luminescent TIM10 yeast counterscreen. | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504657 | Dose Response confirmation of uHTS small molecule inhibitors of tim23-1: a luminescent tim10-1 yeast counterscreen. | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504565 | Dose Response of Developing T Cell Immune Modulators with powder sourced compounds | NMMLSC | 08/03/11 |
| aid504500 | Dose Response of inhibitors of GRK2 binding with RNA aptamer, Cherry Pick 1 | NMMLSC | 08/03/11 |
| aid504330 | Dose response assay for dual activators of procaspase-3 and procaspase-7: Absorbance-based biochemical high throughput screening assay to identify activators of procaspase-7 | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504756 | Dose response confirmation of the uHTS fluorescent assay for identification of inhibitors of ATG4B. | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504328 | Dose response counterscreen for dual activators of procaspase-3 and procaspase-7: Absorbance-based biochemical high throughput screening assay to identify activators of procaspase-3 | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504698 | Fluorescence-based biochemical high throughput dose response assay for activators of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504742 | Fluorescence-based biochemical high throughput dose response assay for inhibitors of the calcium sensitivity of cardiac Regulated Thin Filaments (RTF) | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504699 | Fluorescence-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504453 | Fluorescence-polarization-based biochemical polarscreen dose response binding assay for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg) | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504712 | HTS Dose response counterscreen for assays utilizing the enzyme, beta-galactosidase - Set 3 | Burnham Center for Chemical Genomics | 08/03/11 |
| aid504701 | Homogeneous Time Resolved Fluorescence (HTRF)-based cell-based high throughput dose response assay for antagonists of the orexin 1 receptor (OX1R; HCRTR1) | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504735 | Late stage assay provider counterscreen for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg): Luminescence-based cell-based dose response assay for partial agonists of the peroxisome proliferator-activated receptor alpha (PPARA). | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504460 | Late-stage fluorescence dose response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): purchased compounds EC50 | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504410 | Late-stage radioligand binding dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): PDSP screen Ki Set 2 | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504447 | Luminescence-based cell-based assay provider high throughput dose response assay for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg) | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid504589 | SAR Analysis for the identification of selective inhibits of the transient receptor potential cation channel C4 (TRPC4): Automated Electrophysiology_2 | Johns Hopkins Ion Channel Center | 08/03/11 |
| aid504446 | TR-FRET-based biochemical dose response competitive binding lanthascreen assay for partial agonists of the peroxisome proliferator-activated receptor gamma (PPARg) | The Scripps Research Institute Molecular Screening Center | 08/03/11 |
| aid489014 | Absorbance-based biochemical high throughput dose response assay for activators of procaspase-3 | The Scripps Research Institute Molecular Screening Center | 08/02/11 |
| aid504322 | CHOP dose-response primary assay | Emory University | 08/02/11 |
| aid492957 | Counterscreen for AddAB inhibitors: absorbance-based bacterial cell-based high throughput dose response assay to identify inhibitors of RecBCD | The Scripps Research Institute Molecular Screening Center | 08/02/11 |
| aid489013 | Counterscreen for procaspase-3 activators: absorbance-based biochemical high throughput dose response assay for activators of procaspase-7 | The Scripps Research Institute Molecular Screening Center | 08/02/11 |
| aid493155 | Dose Response confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay | Burnham Center for Chemical Genomics | 08/02/11 |
| aid493182 | Dose Response confirmation of uHTS for the identification of UBC13 Polyubiquitin Inhibitors via a TR-FRET Assay reconfirm | Burnham Center for Chemical Genomics | 08/02/11 |
| aid493003 | Dose Response confirmation of uHTS small molecule inhibitors of tim10-1 yeast via a luminescent assay | Burnham Center for Chemical Genomics | 08/02/11 |
| aid492970 | Fluorescence-based biochemical dose response assay to identify inhibitors of Protein Arginine Deiminase 4 (PAD4) | The Scripps Research Institute Molecular Screening Center | 08/02/11 |
| aid493021 | Inhibitors of T-Type Calcium Channels | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 08/02/11 |
| aid493022 | Inhibitors of T-Type Calcium Channels (SynthLib1) | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 08/02/11 |
| aid493023 | Inhibitors of T-Type Calcium Channels (SynthLib2) | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 08/02/11 |
| aid489010 | Intein inhibitors as potential Tuberculosis drugs | Southern Research Specialized Biocontainment Screening Center | 08/02/11 |
| aid504317 | Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-1 (PLIN1) (2K validation set) | The Scripps Research Institute Molecular Screening Center | 08/02/11 |
| aid504319 | Luminescence-based biochemical high throughput dose response assay for inhibitors of the interaction of the lipase co-activator protein, abhydrolase domain containing 5 (ABHD5) with perilipin-5 (MLDP; PLIN5) (2K validation set) | The Scripps Research Institute Molecular Screening Center | 08/02/11 |
| aid492991 | SAR Analysis for the identification of selective inhibits of the transient receptor potential cation channel C4 (TRPC4): Automated Electrophysiology | Johns Hopkins Ion Channel Center | 08/02/11 |
| aid504313 | XBP1 DR counterscreen for CHOP | Emory University | 08/02/11 |
| aid485288 | A confirmatory biochemical assay using the ADP-Hunter methodology, purified TAg, and ATP to quantify activity of synthesized compounds that inhibit the ATPase activity of Tag (3) | Southern Research Specialized Biocontainment Screening Center | 08/01/11 |
| aid488790 | Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically AGP1 | NMMLSC | 08/01/11 |
| aid488825 | Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically CIT2 | NMMLSC | 08/01/11 |
| aid488823 | Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically LAP4 | NMMLSC | 08/01/11 |
| aid488812 | Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically MEP2 | NMMLSC | 08/01/11 |
| aid488814 | Confirmatory Cherry Pick 3 SAR Dose Response Multiplex in TOR pathway GFP-fusion proteins for Saccharomyes cerevisiae, specifically RPL19A | NMMLSC | 08/01/11 |
| aid463257 | Counterscreen for NR2E3 inverse agonists: TR-FRET-based biochemical high throughput dose response assay to identify inverse agonists of the interaction between peroxisome proliferator-activated receptor gamma (PPARg) and nuclear receptor co-repressor 2 (NCOR2) | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid488861 | Dose Response Confirmation of compounds that inhibit VHR1 in Fluorescent Assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488817 | Dose Response concentration confirmation of uHTS hits from a small molecule activators of human intestinal alkaline phosphatase via a luminescent assay - Set 2 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488783 | Dose Response concentration confirmation of uHTS hits from a small molecule activators of mouse intestinal alkaline phosphatase via a luminescent assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488923 | Dose Response confirmation of compounds that inhibit HePTP | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488863 | Dose Response confirmation of inhibitors of NALP1 in yeast using a Caspase-1-ASC counter screen. | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488800 | Dose Response confirmation of inhibitors of NALP3 in yeast using a Caspase-1-ASC counter screen | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488901 | Dose Response confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Caspase-3 Selectivity assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488920 | Dose Response confirmation of inhibitors of Sentrin-specific proteases (SENPs) using a Luminescent Interference Counterscreen assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488875 | Dose Response confirmation of uHTS activators of Human Intestinal Alkaline Phosphatase using Mouse Intestinal Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488888 | Dose Response confirmation of uHTS activators of Human Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488886 | Dose Response confirmation of uHTS activators of Human Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488873 | Dose Response confirmation of uHTS activators of Mouse Intestinal Alkaline Phosphatase using Human Intestinal Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488878 | Dose Response confirmation of uHTS activators of Mouse Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488880 | Dose Response confirmation of uHTS activators of Mouse Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488921 | Dose Response confirmation of uHTS for inhibitors of Sentrin-specific protease 6 (SENP6) using a Luminescent assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488903 | Dose Response confirmation of uHTS for inhibitors of Sentrin-specific protease 8 (SENP8) using a Luminescent assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488860 | Dose Response confirmation of uHTS for the identification of inhibitors of NALP1 in yeast using a luminescent assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488799 | Dose Response confirmation of uHTS for the identification of inhibitors of NALP3 in yeast using a luminescent assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488748 | Dose Response confirmation of uHTS hits from a small molecule agonists of the APJ receptor via a luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488793 | Dose Response confirmation of uHTS hits from a small molecule inhibitors of human intestinal alkaline phosphatase via a luminescent assay - Set 2 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488785 | Dose Response confirmation of uHTS hits from a small molecule inhibitors of mouse intestinal alkaline phosphatase via a luminescent assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488874 | Dose Response confirmation of uHTS inhibitors of Human Intestinal Alkaline Phosphatase using Mouse Intestinal Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488892 | Dose Response confirmation of uHTS inhibitors of Human Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488882 | Dose Response confirmation of uHTS inhibitors of Human Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488876 | Dose Response confirmation of uHTS inhibitors of Mouse Intestinal Alkaline Phosphatase using Human Intestinal Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488879 | Dose Response confirmation of uHTS inhibitors of Mouse Intestinal Alkaline Phosphatase using Placental Alkaline Phosphatase | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488906 | Dose Response confirmation of uHTS inhibitors of Mouse Intestinal Alkaline Phosphatase using Tissue Nonspecific Alkaline Phosphatase. | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488865 | Dose Response screen for agonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule agonists hits of the APJ receptor | Burnham Center for Chemical Genomics | 08/01/11 |
| aid463220 | Dose Response: Fluorescence polarization-based cell-based high throughput dose response assay for inhibitors of insulin-degrading enzyme (IDE) | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid485352 | HTS Dose response counterscreen for assays utilizing the enzyme, beta-galactosidase - Set 2 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid489005 | Inhibitors of T-Type Calcium Channel | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 08/01/11 |
| aid485336 | Late stage assay provider counterscreen results from the probe development effort to identify inhibitors of kruppel-like factor 5 (KLF5): chemiluminescence-based western blot assay for inhibitors of KLF5 protein levels | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid463225 | Late-stage fluorescence dose response cell-based counterscreening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): inhibition by S1P4-selective antagonist | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid463250 | Late-stage fluorescence-based counterscreen for antagonists of the G-protein coupled receptor 7 (GPR7): cell-based dose response assay to identify antagonists of the melanin-concentrating hormone receptor 1 (MCHR1) | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid463251 | Late-stage fluorescence-based dose response cell-based screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7) | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid485339 | Late-stage fluorescence-based dose response cell-based screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7): Intracellular calcium release | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid463217 | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488987 | SAR Analysis for the identification of Selective Antagonists of ERK1/2 Activity in GPR35-Overexpressing U2OS Cells - Set 2 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488824 | SAR Analysis of Agonists of the DOR Receptor using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488822 | SAR Analysis of Agonists of the MOR Receptor using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488831 | SAR Analysis of Antagonists of the DOR Receptor using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488842 | SAR Analysis of Antagonists of the MOR Receptor using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid463228 | SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid485287 | SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay - Set 4 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488791 | SAR Confirmatory Dose Response LIBS Assay for Allosteric Ligands of the VLA-4 Integrin | NMMLSC | 08/01/11 |
| aid488869 | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 4 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488871 | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 4 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488884 | SAR Selectivity Analysis of small molecule inhibitors of PEST using pCAP in a fluorescence assay | Burnham Center for Chemical Genomics | 08/01/11 |
| aid485286 | SAR analysis of Agonists of the GPR35 Receptor using an Image-Based Assay - Set 4 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488833 | SAR analysis of Agonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay-Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488957 | SAR analysis of Antagonists of IAP-family anti-apoptotic proteins - Set 2 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488963 | SAR analysis of Antagonists of XIAP-Bir3 domain of IAP-family anti-apoptotic proteins - Set 2 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid463227 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 5 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid485283 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 6 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488819 | SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488925 | SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 4 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid485282 | SAR analysis of agonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 4 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid485277 | SAR analysis of agonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid485285 | SAR analysis of antagonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 4 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid485278 | SAR analysis of antagonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488826 | SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 5 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid488935 | SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 6 | Burnham Center for Chemical Genomics | 08/01/11 |
| aid463256 | TR-FRET-based biochemical high throughput dose response assay to identify NR2E3 inverse agonists | The Scripps Research Institute Molecular Screening Center | 08/01/11 |
| aid463108 | Counterscreen for Oxytocin Receptor (OXTR) agonists: Fluorescence-based cell-based high throughput dose response assay to identify agonists of the vasopressin 1 receptor (V1R) | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463128 | Counterscreen for vasopressin 1 receptor (V1R) agonists: Fluorescence-based cell-based high throughput dose response assay for agonists of the Oxytocin Receptor (OXTR) | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid449765 | Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator(PAM) : Activity with human M4 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 07/31/11 |
| aid463120 | Dose Response concentration confirmation of uHTS hits from a small molecule activators of human intestinal alkaline phosphatase via a luminescent assay | Burnham Center for Chemical Genomics | 07/31/11 |
| aid435032 | Dose Response confirmation of HTS hits from an HePTP Fluorescent Assay using OMFP substrate - Set 2 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid435024 | Dose Response confirmation of uHTS hits from a small molecule inhibitors of LYP via a fluorescence intensity assay - Set 2 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid435027 | Dose Response confirmation of uHTS hits from a small molecule inhibitors of LYP via a fluorescence intensity assay using pCAP substrate | Burnham Center for Chemical Genomics | 07/31/11 |
| aid463135 | Dose Response confirmation of uHTS hits from a small molecule inhibitors of human intestinal alkaline phosphatase via a luminescent assay |
Burnham Center for Chemical Genomics | 07/31/11 |
| aid449766 | Dose Response of primary screening hit compounds for Identification of VLA-4 Allosteric Modulators | NMMLSC | 07/31/11 |
| aid463214 | Dose Response screen for antagonists of Angiotensin II Receptor Type 1 to assess selectivity of uHTS small molecule antagonists hits of the APJ receptor | Burnham Center for Chemical Genomics | 07/31/11 |
| aid435026 | Fluorescence Cell-Free Homogeneous Counterscreen to Identify Inhibitors of the RanGTP-Importin-beta complex. | Broad Institute | 07/31/11 |
| aid435023 | Fluorescence Polarization Cell-Free Homogeneous Dose Retest to Confirm Inhibitors of the LANA Histone H2A/H2B Interaction | Broad Institute | 07/31/11 |
| aid463103 | Fluorescence-based cell-based high throughput dose response assay for agonists of the Oxytocin Receptor (OXTR) | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463125 | Fluorescence-based cell-based high throughput dose response assay for potentiators of Oxytocin Receptor (OXTR) | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463127 | Fluorescence-based cell-based high throughput dose response screening assay for agonists of the vasopressin 1 receptor (V1R) | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid435017 | High throughput discovery of novel modulators of ROMK K+ channel activity: Analog Library Testing | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 07/31/11 |
| aid463182 | High throughput fluorescence intensity-based biochemical assay to screen for small molecule inhibitors of Furin:Concentration-response Confirmation Assays | University of Pittsburgh | 07/31/11 |
| aid463081 | Late stage assay provider results from the probe development effort to identify inhibitors of GSTO1: Gel-based activity-based protein profiling (ABPP) IC50 | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463142 | Late stage assay provider results from the probe development effort to identify inhibitors of GSTO1: Gel-based activity-based protein profiling (ABPP) IC50 Set 2 | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463124 | Late stage assay provider results from the probe development effort to identify inhibitors of protein phosphatase methylesterase 1 (PME-1): Gel-based Activity-Based Protein Profiling (ABPP) IC50 Set 2 | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid435013 | Late stage results from the probe development effort to identify inhibitors of (NADPH oxidase 1) NOX1: Family selectivity: Set 2 | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463107 | Late-stage fluorescence dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Synthesized compounds | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463118 | Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 1 (S1P1) counterscreen assay | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463122 | Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 2 (S1P2) counterscreen assay | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463123 | Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 3 (S1P3) counterscreen assay | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463129 | Late-stage fluorescence-based dose-response cell-based assay to identify agonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Sphingosine 1-Phosphate Receptor 5 (S1P5) counterscreen assay | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463088 | Luminescence-based cell-based high throughput dose response assay for activators of the Aryl Hydrocarbon Receptor (AHR) | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid463086 | Luminescence-based counterscreen for activators of the Aryl Hydrocarbon Receptor (AHR): cell-based high throughput dose response screening assay for activators of the Pregnane X Receptor (PXR) | The Scripps Research Institute Molecular Screening Center | 07/31/11 |
| aid435014 | Measurement of GPCR-mediated thallium flux through GIRK channels: Dose-Response Testing | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 07/31/11 |
| aid435016 | Measurement of GPCR-mediated thallium flux through GIRK channels: Dose-Response with Rauwolscine | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 07/31/11 |
| aid449726 | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 3 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid449727 | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 3 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid435018 | SAR analysis for the identification of translation initiation inhibitors (PABP) | Burnham Center for Chemical Genomics | 07/31/11 |
| aid435011 | SAR analysis for the identification of translation initiation inhibitors (eIF4H) | Burnham Center for Chemical Genomics | 07/31/11 |
| aid449736 | SAR analysis of compounds that inhibit HePTP - Set 2 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid435029 | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion, cell-cell fusion assay | Burnham Center for Chemical Genomics | 07/31/11 |
| aid449733 | SAR analysis of compounds that inhibit VHR1, Fluorescent Assay - Set 2 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid449737 | SAR analysis of small molecule agonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 3 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid463105 | SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 4 | Burnham Center for Chemical Genomics | 07/31/11 |
| aid434976 | Counterscreen for inhibitors of gld-1: Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of the HIV Rev protein-RRE RNA interaction | The Scripps Research Institute Molecular Screening Center | 07/30/11 |
| aid434968 | Fluorescence Cell-Free Homogeneous Counter Screen to Identify Inhibitors of GFP Chromophore Formation | Broad Institute | 07/30/11 |
| aid435010 | Fluorescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of RecA-Intein Splicing Activity | Broad Institute | 07/30/11 |
| aid435009 | Late stage results from the probe development effort to identify inhibitors of (NADPH oxidase 1) NOX1: Xanthine Oxidase Set 2 | The Scripps Research Institute Molecular Screening Center | 07/30/11 |
| aid435002 | Late stage results from the probe development effort to identify inhibitors of NOX1: HEK/293 IC50 Set 2 | The Scripps Research Institute Molecular Screening Center | 07/30/11 |
| aid434957 | Late stage results from the probe development effort to identify inhibitors of kruppel-like factor 5 (KLF5): luminescence-based cell-based dose response assay for inhibitors of KLF5 (Round 1) | The Scripps Research Institute Molecular Screening Center | 07/30/11 |
| aid435004 | Luminescence Cell-Based Dose Retest to Identify Potentiators of Heat Shock Factor 1 (HSF1) | Broad Institute | 07/30/11 |
| aid434997 | Luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Cherry picks 2 | The Scripps Research Institute Molecular Screening Center | 07/30/11 |
| aid434967 | SAR analysis of compounds that inhibit Human Immunodeficiency Virus Fusion. | Burnham Center for Chemical Genomics | 07/30/11 |
| aid434981 | SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 3 | Burnham Center for Chemical Genomics | 07/30/11 |
| aid434980 | SAR analysis of small molecule inhibitors of Mint-PDZ and N-type Ca2+ channel carboxyl-terminal peptide association using HTRF - Set 2 | Burnham Center for Chemical Genomics | 07/30/11 |
| aid434943 | Absorbance Microorganism Dose Response to Identify Inhibitors of Vibrio harveyi | Broad Institute | 07/29/11 |
| aid434935 | Fluorescence Cell-Based Secondary Assay of Resistant C. albicans Growth in the Presence of Fluconazole | Broad Institute | 07/29/11 |
| aid434945 | Fluorescence Cell-Based Secondary Assay to Identify Inhibitors of Calcineurin | Broad Institute | 07/29/11 |
| aid434940 | Late stage counterscreen results from the probe development effort to identify activators of signal transducer and activator of transcription 1 (STAT1): luminescence-based cell-based dose response assay for STAT3 activators | The Scripps Research Institute Molecular Screening Center | 07/29/11 |
| aid434932 | Late stage results from the probe development effort to identify activators of signal transducer and activator of transcription 1 (STAT1): luminescence-based cell-based dose response assay for STAT1 activators | The Scripps Research Institute Molecular Screening Center | 07/29/11 |
| aid434938 | Luminescence Cell-Based Secondary Assay to Identify Inhibitors of Hsp90 | Broad Institute | 07/29/11 |
| aid434944 | Luminescence Cell-Free Homogeneous Dose Response to Identify Inhibitors of Lux-S | Broad Institute | 07/29/11 |
| aid434954 | Luminescence Cell-Free Homogeneous Dose Retest to Identify Inhibitors of Glycogen Synthase Kinase-3 beta Activity | Broad Institute | 07/29/11 |
| aid434924 | SAR analysis of Agonists of the GPR35 Receptor using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 07/29/11 |
| aid434925 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 4 | Burnham Center for Chemical Genomics | 07/29/11 |
| aid434928 | SAR analysis of agonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 2 | Burnham Center for Chemical Genomics | 07/29/11 |
| aid434929 | SAR analysis of antagonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 3 | Burnham Center for Chemical Genomics | 07/29/11 |
| aid434922 | SAR analysis of antagonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 2 | Burnham Center for Chemical Genomics | 07/29/11 |
| aid2784 | Dose Response confirmation of uHTS hits from a small molecule antagonists of the APJ receptor via a luminescent beta-arrestin assay | Sanford-Burnham Center for Chemical Genomics | 07/12/11 |
| aid2828 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao with additional round of SAR compounds | NMMLSC | 07/12/11 |
| aid2829 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao with additional round of SAR compounds. | NMMLSC | 07/12/11 |
| aid2826 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao with additional round of SAR compounds. | NMMLSC | 07/12/11 |
| aid2827 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao with additional round of SAR compounds | NMMLSC | 07/12/11 |
| aid2841 | Dose-response primary assay and counterscreen assay for HTS small molecule inhibitors of CHOP to regulate the unfolded protein response to ER stress | Emory University | 07/12/11 |
| aid2802 | Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of GLD-1 protein - TGE RNA interaction | The Scripps Research Institute Molecular Screening Center | 07/12/11 |
| aid2771 | Late stage counterscreen results from the probe development effort to identify STAT1 inhibitors: luminescence-based cell-based dose response assay for STAT3 inhibitors | The Scripps Research Institute Molecular Screening Center | 07/12/11 |
| aid2772 | Late stage results from the probe development effort to identify STAT1 inhibitors: luminescence-based cell-based dose response assay for STAT1 inhibitors | The Scripps Research Institute Molecular Screening Center | 07/12/11 |
| aid2808 | Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Purchased analogs | The Scripps Research Institute Molecular Screening Center | 07/12/11 |
| aid2819 | Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Purchased analogs 2 | The Scripps Research Institute Molecular Screening Center | 07/12/11 |
| aid2773 | Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Synthesized analogs 3 | The Scripps Research Institute Molecular Screening Center | 07/12/11 |
| aid2821 | Luminescence Cell-Free Homogenous Dose Retest to Identify Inhibitors of Serine/Threonine Kinase 33 Activity | Broad Institute | 07/12/11 |
| aid2793 | SAR analysis of NF-kappaB dependent luciferase using DAP as an inducer - Set 2 | Burnham Center for Chemical Genomics | 07/12/11 |
| aid2789 | SAR analysis of NF-kappaB dependent luciferase using Doxorucibin as an inducer - Set 2 | Burnham Center for Chemical Genomics | 07/12/11 |
| aid2792 | SAR analysis of NF-kappaB dependent luciferase using PMA/Ionomycin as an inducer - 2 | Burnham Center for Chemical Genomics | 07/12/11 |
| aid2798 | SAR analysis of compounds that inhibit NOD1 - Set 3 | Burnham Center for Chemical Genomics | 07/12/11 |
| aid2799 | SAR analysis of compounds that inhibit NOD2 - Set 3 | Burnham Center for Chemical Genomics | 07/12/11 |
| aid2801 | SAR analysis of inhibitors of TNFa specific NF-kB induction - Set 3 | Burnham Center for Chemical Genomics | 07/12/11 |
| aid2723 | Absorbance Microorganism Dose Retest to Identify Inhibitors of Vibrio harveyi | Broad Institute | 07/11/11 |
| aid2470 | Absorbance Microorganism-Based Dose Response Followup to Identify Inhibitors of Streptokinase Expression. | Broad Institute | 07/11/11 |
| aid2725 | Absorbance Microorganism-Based Dose Retest to Identify Inhibitors of Vibrio harveyi | Broad Institute | 07/11/11 |
| aid2594 | Confirmation dose response assay for compounds that inhibit/block inward-rectifying potassium ion channel Kir2.1 | Johns Hopkins Ion Channel Center | 07/11/11 |
| aid2759 | Counterscreen for agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3): TR-FRET-based biochemical high throughput dose response assay to identify agonists of the interaction between peroxisome proliferator-activated receptor gamma (PPARg) and nuclear receptor co-repressor 2 (NCOR2) | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2651 | Discovery of Novel Allosteric Modulators of the M1 Muscarinic Receptor: PAM Calcium Assay SAR | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 07/11/11 |
| aid2428 | Discovery of novel allosteric modulators of the M1 muscarinic receptor: PAM Calcium Assay Dose-Response with M3 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 07/11/11 |
| aid2638 | Dosage response for compounds that protect hERG from block by proarrhythmic agents using manual patch clamp | Johns Hopkins Ion Channel Center | 07/11/11 |
| aid2743 | Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically AGP1 based on MLPCN hits | NMMLSC | 07/11/11 |
| aid2744 | Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically CIT2 based on MLPCN hits | NMMLSC | 07/11/11 |
| aid2745 | Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically LAP4 based on MLPCN hits | NMMLSC | 07/11/11 |
| aid2742 | Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically MEP2 based on MLPCN hits | NMMLSC | 07/11/11 |
| aid2740 | Dose Response of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae specifically RPL19A based on MLPCN hits | NMMLSC | 07/11/11 |
| aid2654 | Dose response of Retigabine-insensitive compounds that potentiate KCNQ2 potassium channel | Johns Hopkins Ion Channel Center | 07/11/11 |
| aid2755 | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput counterscreen to identify inhibitors of TEM-1 metallo-beta-lactamase | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2756 | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of IMP-1metallo-beta-lactamase | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2754 | Epi-absorbance-based dose response assay for common IMP-1 and VIM-2 inhibitors: biochemical high throughput screening assay to identify inhibitors of VIM-2 metallo-beta-lactamase | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2579 | G6DPH counterscreen for TbHK1 inhibitors - Analogues series | University of Pittsburgh | 07/11/11 |
| aid2485 | HTS dose response assay for identification of inhibitors of TNFa-specific NF-kB induction | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2583 | Late stage counterscreen for the probe development effort to identify selective agonists of the Transient Receptor Potential Channels 3 (TRPML3): fluorescence-based cell-based dose response assay for TRPN1 agonists. | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2556 | Late stage results from the probe development effort to identify inhibitors of (NADPH oxidase 1) NOX1: Xanthine Oxidase | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2532 | Late stage results from the probe development effort to identify inhibitors of NOX1: HEK/293 IC50 | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2510 | Late stage results from the probe development effort to identify selective agonists of the Transient Receptor Potential Channels 3 (TRPML3): fluorescence-based cell-based dose response assay for TRPML3 agonists | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2664 | Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Synthesized analogs | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2752 | Late-stage luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1): Synthesized analogs 2 | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2765 | Luminescence Cell-Based Dose Retest to Identify Inhibitors of A1 Apoptosis | Broad Institute | 07/11/11 |
| aid2735 | Luminescence Microorganism Dose Retest to Identify Inhibitors of the AI-2 Quorum Sensing System | Broad Institute | 07/11/11 |
| aid2724 | Luminescence Microorganism-Based Dose Retest to Identify Modulators of the AI-2 Quorum Sensing System | Broad Institute | 07/11/11 |
| aid2538 | Luminescence-based cell-based dose response assay to identify inhibitors of NADPH oxidase 1 (NOX1) | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2443 | Mode of action - deactivation constant concentration response for ztz240, a potentiator of KCNQ2 potassium channels | Johns Hopkins Ion Channel Center | 07/11/11 |
| aid2603 | Mode of action assay-Automated electrophysiology assay of compounds that potentiate KCNQ2 potassium channel | Johns Hopkins Ion Channel Center | 07/11/11 |
| aid2493 | SAR Analysis of Agonists of the DOR Receptor using an Image-Based Assay - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2492 | SAR Analysis of Agonists of the MOR Receptor using an Image-Based Assay - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2686 | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2682 | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2497 | SAR analysis of Agonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2480 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2491 | SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2505 | SAR analysis of GM-Tri-DAP induced IL-8 secretion in MCF-7/NOD1 cells - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2503 | SAR analysis of Muramyl dipeptide (MDP) induced IL-8 secretion in MCF-7/NOD2 cells - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2504 | SAR analysis of Tumor necrosis factor alpha (TNF-alpha) induced IL-8 secretion in MCF-7/NOD1 cells - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2466 | SAR analysis of compounds that inhibit NOD1 - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2475 | SAR analysis of compounds that inhibit NOD2 - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2483 | SAR analysis of inhibitors of TNFa specific NF-kB induction - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2500 | SAR analysis of small molecule agonists of the kappa opioid receptor via a luminescent beta-arrestin assay - Set 2 | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2489 | SAR analysis of small molecule inhibitors of Mint-PDZ and N-type Ca2+ channel carboxyl-terminal peptide association using HTRF | Burnham Center for Chemical Genomics | 07/11/11 |
| aid2758 | TR-FRET-based biochemical high throughput dose response assay for agonists of nuclear receptor subfamily 2, group E, member 3 (NR2E3) | The Scripps Research Institute Molecular Screening Center | 07/11/11 |
| aid2377 | Counterscreen for inhibitors of EBNA-1: fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors of the Epstein-Barr virus-encoded protein, ZTA | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2422 | Counterscreen for inhibitors of PP1: fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Protein Phosphatase 5 (PP5) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2394 | Counterscreen for inhibitors of PP5: fluorescence-based biochemical high throughput dose response assay for inhibitors of Protein Phosphatase 1 (PP1) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2423 | Fluorescence Cell-Based Secondary Assay to Identify Inhibitors of Resistant C. albicans Growth in the Presence of Fluconazole | Broad Institute | 07/10/11 |
| aid2387 | Fluorescence Cell-Based Secondary Assay to Measure Toxicity of Compounds Not in the Presence of Fluconazole | Broad Institute | 07/10/11 |
| aid2381 | Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of the Epstein-Barr virus nuclear antigen 1 (EBNA-1) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2395 | Fluorescence-based biochemical high throughput dose response assay for inhibitors of Protein Phosphatase 5 (PP5) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2403 | Fluorescence-based biochemical high throughput dose response assay to identify inhibitors of Protein Phosphatase 1 (PP1) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2343 | HTS Image-Based Screen for Agonists of the DOR Receptor | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2356 | HTS Image-Based Screen for Antagonists of the DOR Receptor | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2351 | Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2354 | Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 2 (S1P2) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2349 | Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 3 (S1P3) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2350 | Late stage counterscreen assay for S1P4 antagonists: Fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 5 (S1P5) | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2346 | Late stage fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4): Synthesized analogues | The Scripps Research Institute Molecular Screening Center | 07/10/11 |
| aid2382 | Luminescence Cell-Based Dose Confimation HTS to Identify Inhibitors of Heat Shock Factor 1 (HSF1) | Broad Institute | 07/10/11 |
| aid2388 | Luminesence Cell-Based Secondary Assay to Identify Inhibitors of Calcineurin | Broad Institute | 07/10/11 |
| aid2400 | Luminesence Cell-Based Secondary Assay to Identify Inhibitors of Hsp90 | Broad Institute | 07/10/11 |
| aid2408 | Mode of action - current amplitude concentration response for ztz240, a potentiator of KCNQ2 potassium channels | Johns Hopkins Ion Channel Center | 07/10/11 |
| aid2370 | SAR Analysis of Agonists of the DOR Receptor using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2352 | SAR Analysis of Agonists of the MOR Receptor using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2357 | SAR Analysis of Antagonists of the DOR Receptor using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2420 | SAR Analysis of Antagonists of the MOR Receptor using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2397 | SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2359 | SAR analysis of Agonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2338 | SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2348 | SAR analysis of Antagonists of the Kappa Opioid Receptor (KOR) using an Image-Based Assay | Burnham Center for Chemical Genomics | 07/10/11 |
| aid2230 | Confirmation assay for inhibitors of Trypanosoma brucei hexokinase 1-Analogue-first series | University of Pittsburgh | 07/09/11 |
| aid2214 | Counterscreen for inhibitors of M1 and M17 aminopeptidases: QFRET-based biochemical high throughput dose response assay for inhibitors of the Cathepsin L proteinase (CTSL1). | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2218 | Counterscreen for inhibitors of MCL1: fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of BCL2-related protein, long isoform (BCLXL). | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2204 | Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: Calcium Flux Assay | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 07/09/11 |
| aid2298 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao for SAR Compounds | NMMLSC | 07/09/11 |
| aid2311 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao for SAR Compounds | NMMLSC | 07/09/11 |
| aid2295 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao for SAR compounds | NMMLSC | 07/09/11 |
| aid2296 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao for SAR Compounds | NMMLSC | 07/09/11 |
| aid2307 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao for SAR Compounds | NMMLSC | 07/09/11 |
| aid2207 | Fluorescence counterscreen for potentiators or agonists of NPY-Y1: Cell-based high-throughput dose response assay for potentiators or agonists of NPY-Y2. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2217 | Fluorescence polarization-based biochemical high throughput dose response assay for inhibitors of myeloid cell leukemia sequence 1 (MCL1) interactions with BIM-BH3 peptide. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2210 | Fluorescence-based cell-based high-throughput dose response assay for agonists of NPY-Y2. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2220 | Fluorescence-based cell-based high-throughput dose response assay for potentiators or agonists of NPY-Y2. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2219 | Fluorescence-based counterscreen for agonists of NPY-Y1: cell-based high-throughput dose response assay for agonists of NPY-Y2. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2212 | Fluorescence-based counterscreen for agonists of NPY-Y2: cell-based high-throughput dose response assay for agonists of NPY-Y1. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2211 | Fluorescence-based counterscreen for potentiators or agonists of NPY-Y2: cell-based high-throughput dose response assay for potentiators or agonists of NPY-Y1. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2251 | Fluorescence-based dose response cell-based high throughput screening assay to identify antagonists of the G-protein coupled receptor 7 (GPR7). | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2208 | Fluorescence-based dose response cell-based high-throughput screening assay for agonists of NPY-Y1. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2209 | Fluorescence-based dose response cell-based high-throughput screening assay for potentiators or agonists of NPY-Y1. | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2073 | Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | Burnham Center for Chemical Genomics | 07/09/11 |
| aid1903 | Identification of SV40 T antigen inhibitors: A route to novel anti-viral reagents | Southern Research Specialized Biocontainment Screening Center | 07/09/11 |
| aid2013 | Image-Based HTS for Selective Antagonists for GPR55 | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2058 | Image-Based HTS for Selective Antagonists of GPR35 | Burnham Center for Chemical Genomics | 07/09/11 |
| aid1961 | Image-based HTS for Selective Agonists of GPR55 | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2332 | Late stage fluorescence dose response cell-based screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 4 (S1P4) | The Scripps Research Institute Molecular Screening Center | 07/09/11 |
| aid2264 | SAR analysis of NF-kB dependent luciferase using DAP as an inducer | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2333 | SAR analysis of compounds that inhibit NOD1 revised | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2334 | SAR analysis of compounds that inhibit NOD2 revised | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2337 | SAR analysis of inhibitors of TNFa specific NF-kB induction revised | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2284 | SAR analysis of small molecule agonists of the kappa opioid receptor via a luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2285 | SAR analysis of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2006 | uHTS HTRF assay for identification of inhibitors of SUMOylation | Burnham Center for Chemical Genomics | 07/09/11 |
| aid1654 | uHTS absorbance assay for the identification of compounds that inhibit VHR1. | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2014 | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (PABP) | Burnham Center for Chemical Genomics | 07/09/11 |
| aid2012 | uHTS fluorescence polarization assay for the identification of translation initiation inhibitors (eIF4H) | Burnham Center for Chemical Genomics | 07/09/11 |
| aid1817 | uHTS identification of small molecule antagonists of the binding of Siah-1 and a peptide ligand via a fluorescence polarization assay. | Burnham Center for Chemical Genomics | 07/09/11 |
| aid1778 | uHTS identification of small molecule antagonists of the kappa opioid receptor via a luminescent beta-arrestin assay | Burnham Center for Chemical Genomics | 07/09/11 |
| aid1779 | uHTS identification of small molecule inhibitors of LYP via a fluorescence intensity assay | Burnham Center for Chemical Genomics | 07/09/11 |
| aid1018 | Chemical Antagonists IAP-family anti-apoptotic proteins | Sanford-Burnham Center for Chemical Genomics | 07/08/11 |
| aid1619 | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | SRMLSC | 07/08/11 |
| aid696 | Luminescent assay for HTS discovery of chemical activators of placental alkaline phosphatase | Burnham Center for Chemical Genomics | 07/08/11 |
| aid1001 | uHTS identification of compounds activating TNAP in the absence of phosphate acceptor performed in luminescent assay | Sanford-Burnham Center for Chemical Genomics | 07/08/11 |
| aid1578 | uHTS luminescence assay for the identification of compounds that inhibit NOD1 | Burnham Center for Chemical Genomics | 07/08/11 |
| aid2102 | Identification of SV40 T antigen inhibitors: Cytotoxicity screen of selected hits | Southern Research Specialized Biocontainment Screening Center | 06/09/11 |
| aid2009 | Oxadiazole SAR compounds tested by Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant | NMMLSC | 06/09/11 |
| aid1914 | Absorbance Microorganism-Based Dose Response HTS to Identify Inhibitors of Streptokinase Expression | Broad Institute | 06/08/11 |
| aid1435 | Homologous Recombination - Rad 51_Dose response | PCMD | 06/08/11 |
| aid1431 | Kallikrein 5 1536 HTS Dose Response Confirmation | PCMD | 06/08/11 |
| aid1275 | Dose Response Confirmation for small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) | Emory University | 06/07/11 |
| aid2137 | Absorbance Microorganism-Based Dose Response Followup to Identify Inhibitors of Streptokinase Expression | Broad Institute | 06/05/11 |
| aid2021 | Additional SAR compounds tested by Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant | NMMLSC | 06/05/11 |
| aid2022 | Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype | NMMLSC | 06/05/11 |
| aid2046 | Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype | NMMLSC | 06/05/11 |
| aid2036 | Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype | NMMLSC | 06/05/11 |
| aid2039 | Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant | NMMLSC | 06/05/11 |
| aid2040 | Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype | NMMLSC | 06/05/11 |
| aid2043 | Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant | NMMLSC | 06/05/11 |
| aid2038 | Additional SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | NMMLSC | 06/05/11 |
| aid2018 | AlphaScreen confirmatory assay for validation of inhibitors of SUMOylation | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2075 | Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2 | NMMLSC | 06/05/11 |
| aid2077 | Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B | NMMLSC | 06/05/11 |
| aid2081 | Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W | NMMLSC | 06/05/11 |
| aid2084 | Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL | NMMLSC | 06/05/11 |
| aid2080 | Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1 | NMMLSC | 06/05/11 |
| aid2086 | Confirmation dose response of hits from multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1 | NMMLSC | 06/05/11 |
| aid2167 | Counterscreen for inhibitors of tRNA 2'-phosphotransferase (TPT1): fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors of RNAse T1. | The Scripps Research Institute Molecular Screening Center | 06/05/11 |
| aid2186 | Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: Fold-shift Assay | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2192 | Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: [3H]N-methylscopolamine Competition | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2194 | Discovery of Novel Allosteric Modulators of the Muscarinic Receptor M5: [3H]N-methylscopolamine Competition with Acetylcholine | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2150 | Dose Response of SAR compounds via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype | NMMLSC | 06/05/11 |
| aid2160 | Fluorescence polarization-based biochemical high throughput dose response assay to identify inhibitors of tRNA 2'-phosphotransferase (TPT1). | The Scripps Research Institute Molecular Screening Center | 06/05/11 |
| aid2173 | Fluorescence-based biochemical high throughput dose response assay for inhibitors of the Hepatitis C Virus non-structural protein 3 helicase (NS3). | The Scripps Research Institute Molecular Screening Center | 06/05/11 |
| aid2141 | HTS TR-FRET-based dose response confirmatory assay for Siah-1 | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2134 | HTS HePTP Fluorescent Assay using OMFP substrate for In Vitro dose response studies | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2133 | HTS Image-Based Screen for Selective Agonists of the KOR Receptor | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2136 | HTS Image-Based Screen for Selective Antagonists of the KOR Receptor | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2127 | HTS fluorescence polarization-based dose response confirmatory screen for the Siah-1 primary assay utilizing an alternative fluorophore, fluorescein-labeled plectin | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2126 | LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies. | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2068 | MOA HePTP Fluorescent secondary assay for identification of redox-state modulating compounds | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2070 | MOA VHR1 Fluorescent secondary assay for identification of redox-state modulating compounds | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2197 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Potency at human mGluR4 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2185 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Rat PAM Potency | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2193 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR1 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2188 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR2 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2190 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR3 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2183 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR4 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2199 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR5 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2191 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR6 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2182 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR7 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2181 | Modulation of the Metabotropic Glutamate Receptor mGluR4: Selectivity at mGluR8 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 06/05/11 |
| aid2037 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype | NMMLSC | 06/05/11 |
| aid2033 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype | NMMLSC | 06/05/11 |
| aid2031 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype | NMMLSC | 06/05/11 |
| aid2051 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant | NMMLSC | 06/05/11 |
| aid2027 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype | NMMLSC | 06/05/11 |
| aid2042 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant | NMMLSC | 06/05/11 |
| aid2053 | Oxadiazole SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | NMMLSC | 06/05/11 |
| aid2020 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant | NMMLSC | 06/05/11 |
| aid2019 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 wildtype protein | NMMLSC | 06/05/11 |
| aid2045 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype | NMMLSC | 06/05/11 |
| aid2041 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab7 wildtype | NMMLSC | 06/05/11 |
| aid2048 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 activated mutant | NMMLSC | 06/05/11 |
| aid2055 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac1 wildtype | NMMLSC | 06/05/11 |
| aid2050 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras activated mutant | NMMLSC | 06/05/11 |
| aid2047 | Pyrazoline SAR compounds tested via Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | NMMLSC | 06/05/11 |
| aid2195 | QFRET-based biochemical high throughput dose response assay for inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | The Scripps Research Institute Molecular Screening Center | 06/05/11 |
| aid2196 | QFRET-based counterscreen for inhibitors of PFM18AAP: biochemical high throughput dose response assay for inhibitors of the Cathepsin L proteinase (CTSL1). | The Scripps Research Institute Molecular Screening Center | 06/05/11 |
| aid2151 | SAR Compounds tested by Dose Response Screen via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Mutant. | NMMLSC | 06/05/11 |
| aid2145 | SAR Compounds tested by Dose Response Screen via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 3 Wildtype. | NMMLSC | 06/05/11 |
| aid2140 | SAR LYP1 Fluorescent Assay using OMFP substrate for In Vitro dose response studies | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2135 | SAR LYP1 Fluorescent Assay using pCAP substrate for In Vitro dose response studies | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2159 | TR-FRET-based biochemical high-throughput dose response assay to identify inhibitors of Hepatitis C Virus (HCV) core protein dimerization. | The Scripps Research Institute Molecular Screening Center | 06/05/11 |
| aid2091 | uHTS Homogeneous Terbium Time-Resolved Fluorescence Resonance Energy Transfer (HTRF) Assay | Burnham Center for Chemical Genomics | 06/05/11 |
| aid2001 | uHTS luminescence assay for the identification of compounds that inhibit NOD2 in MDP treated cells | Burnham Center for Chemical Genomics | 06/05/11 |
| aid702 | Dose-Response of Allosteric Antagonists for the VLA-4 Integrin | NMMLSC | 06/04/11 |
| aid521 | HTS Discovery of Chemical Inhibitors of HePTP, a Leukemia Target | Burnham Center for Chemical Genomics | 06/04/11 |
| aid1209 | HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | Sanford-Burnham Center for Chemical Genomics | 06/04/11 |
| aid568 | High Throughput Screening Assay for Hsc70 Inhibitors | Burnham Center for Chemical Genomics | 06/04/11 |
| aid1445 | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) | SRMLSC | 06/04/11 |
| aid425 | MKP-3 in vitro HTS assay | Sanford-Burnham Center for Chemical Genomics | 06/04/11 |
| aid1920 | Epi-absorbance-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. | The Scripps Research Institute Molecular Screening Center | 06/01/11 |
| aid1919 | Epi-absorbance-based dose response biochemical high throughput screening assay for selective inhibitors of VIM-2 metallo-beta-lactamase | The Scripps Research Institute Molecular Screening Center | 06/01/11 |
| aid1926 | FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify epi-absorbance assay artifacts. | The Scripps Research Institute Molecular Screening Center | 06/01/11 |
| aid1927 | FRET-based counterscreen for selective VIM-2 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of IMP-1 metallo-beta-lactamase. | The Scripps Research Institute Molecular Screening Center | 06/01/11 |
| aid1960 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 | Broad Institute | 06/01/11 |
| aid1964 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of POS-1 Binding to mex-3-RNA | Broad Institute | 06/01/11 |
| aid1636 | Cathepsin L probe #2 dose-response testing | PCMD | 05/31/11 |
| aid1764 | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS competition at M3 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/31/11 |
| aid1895 | Dose Response Confirmation Screen via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Mutant | NMMLSC | 05/31/11 |
| aid1897 | Dose Response Confirmation via Multiplex HTS Assay for Inhibitors of MEK Kinase PB1 Domains, specifically MEK5 binding to MEK Kinase 2 Wildtype | NMMLSC | 05/31/11 |
| aid1872 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS4-Galphao. | NMMLSC | 05/31/11 |
| aid1442 | E3 Ligase_Mutant_Dose Response | PCMD | 05/31/11 |
| aid1444 | E3 Ligase_WT_Dose Response | PCMD | 05/31/11 |
| aid1682 | Fluorescence counterscreen assay for TRPML3 agonists: dose response cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel N1 (TRPN1) | The Scripps Research Institute Molecular Screening Center | 05/31/11 |
| aid1660 | Fluorescence counterscreen assay for TRPN1 agonists: dose response cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel ML3 (TRPML3) | The Scripps Research Institute Molecular Screening Center | 05/31/11 |
| aid1878 | Fluorescent assay for identification of compounds that inhibit VHR1 | Burnham Center for Chemical Genomics | 05/31/11 |
| aid1436 | Homologous Recombination_Rad51_DNA binding assay | PCMD | 05/31/11 |
| aid1437 | Homologous recombination_Rad 51_dose response_2 | PCMD | 05/31/11 |
| aid1723 | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Dose-Dependent Assay 2 with KCC2 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/31/11 |
| aid1695 | Rml C and D dose-response confirmation | PCMD | 05/31/11 |
| aid1659 | SAR assay for compounds activating TNAP in the presence of 100 mM DEA performed in a luminescence assay | Burnham Center for Chemical Genomics | 05/31/11 |
| aid858 | Allosteric Modulators of D1 Receptors: Dose-dependent Assay | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/30/11 |
| aid857 | Allosteric Modulators of D1 Receptors: Dose-dependent Counterscreen | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/30/11 |
| aid1417 | Dose Response Confirmation for Mcl-1/Noxa Interaction Inhibitors | Emory University | 05/30/11 |
| aid1419 | Dose Response Confirmation for Small Molecule Inhibitors of Epstein-Barr Virus | Emory University | 05/30/11 |
| aid855 | Dose Response Confirmation for Small Molecule Inhibitors of Eukaryotic Translation Initiation | Emory University | 05/30/11 |
| aid733 | Estrogen Receptor-beta Coactivator Binding Inhibitors Dose Response Confirmation | Emory University | 05/30/11 |
| aid1060 | Estrogen Receptor-beta Coactivator Binding Inhibitors ELISA Secondary Assay | Emory University | 05/30/11 |
| aid618 | Luminescent HTS for small molecule inhibitors of MT1-MMP transcription | Sanford-Burnham Center for Chemical Genomics | 05/30/11 |
| aid1241 | Name: High Throughput Screen to Identify Compounds that increase expression of NF-kB in Human Neuronal Cells - Dose Response | SRMLSC | 05/30/11 |
| aid1938 | Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator (PAM): Analog Dose Response with rM4 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/29/11 |
| aid1939 | Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator (PAM): NMS Competition at rM4 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/29/11 |
| aid1923 | Discovery of a Highly Selective in vitro and in vivo M4 Positive Allosteric Modulator(PAM): Analog Potency | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/29/11 |
| aid1767 | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS competition at M2 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/29/11 |
| aid1757 | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS competition at M4 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/29/11 |
| aid1690 | Dose Response for ABC transporter inhibitors: specifically ABCG2 screen, ABCB1 counter-screen | NMMLSC | 05/29/11 |
| aid1888 | Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS16-Galphao. | NMMLSC | 05/29/11 |
| aid1869 | Dose respone, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS8-Galphao. | NMMLSC | 05/29/11 |
| aid1884 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS19-Galphao. | NMMLSC | 05/29/11 |
| aid1871 | Dose response, multiplexed high-throughput screen for small molecule regulators of RGS family protein interactions, specifically RGS7-Galphao. | NMMLSC | 05/29/11 |
| aid1701 | Fluorescence-based counterscreen assay for S1P4 agonists: Cell-based dose response high throughput screening assay to identify agonists of the Sphingosine 1-Phosphate Receptor 1 (S1P1) | The Scripps Research Institute Molecular Screening Center | 05/29/11 |
| aid1966 | HTS Dose response counterscreen for assays utilizing the enzyme, b-galactosidase | Burnham Center for Chemical Genomics | 05/29/11 |
| aid1736 | Identification of Novel Modulators of Cl- dependent Transport Process via HTS; Dose-dependent Assay with KCC2 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/29/11 |
| aid1913 | Luminescence-based dose response biochemical high throughput screening assay for inhibitors of the Heat Shock Protein 90 (HSP90) | The Scripps Research Institute Molecular Screening Center | 05/29/11 |
| aid1699 | Luminescent counterscreen for inhibitors of the Janus kinase 2 mutant JAK2V617F: dose response cell-based high throughput screening assay for inhibitors of parental Ba/F3 cell viability. | The Scripps Research Institute Molecular Screening Center | 05/29/11 |
| aid1769 | Profiling Assay to determine GST-GSH interactions in multiplex bead-based assays | NMMLSC | 05/29/11 |
| aid1890 | QFRET-based dose response biochemical high throughput screening assay to identify inhibitors of the SARS coronavirus 3C-like Protease (3CLPro) | The Scripps Research Institute Molecular Screening Center | 05/29/11 |
| aid1957 | SAR VHR1 Fluorescent Assay for In Vitro dose response studies | Burnham Center for Chemical Genomics | 05/29/11 |
| aid1958 | SAR VHR1 absorbance Assay for In Vitro dose response studies. | Burnham Center for Chemical Genomics | 05/29/11 |
| aid1941 | SAR assay for compounds inhibiting TNAP in the absence of phosphate acceptor performed in a luminescent assay | Burnham Center for Chemical Genomics | 05/29/11 |
| aid1627 | Cathepsin L dose-response testing in the presence of cysteine | PCMD | 05/28/11 |
| aid936 | Concentration Response Redox Cycling H2O2 Generation assay, 1 mM DTT, to characterize small molecule inhibitors identified in the Polo box domain (PBD) of Plk1 Primary HTS. | University of Pittsburgh | 05/28/11 |
| aid1057 | Concentration Response fluorescence polarization-based assay to test PMLSC Chemistry Core synthesized analogs of confirmed hits from the Polo box domain (PBD) of Plk1 Primary HTS. | University of Pittsburgh | 05/28/11 |
| aid1536 | Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate. | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1535 | Confirmation of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay. | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1514 | Counter Screen using XIAP-Bir3 of the Chemical Antagonists of IAP-family anti-apoptotic proteins confirmation assay | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1655 | Counter screen SAR assay for PMM2 inhibitors via a fluorescence intensity assay | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1528 | Counterscreen assay for PERK inhibitors: Dose response cell-based high throughput screening assay to measure inhibition of PERK at 6 hours | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid874 | Counterscreen for S1P2 Agonists: Dose Response High Throughput Cell-Based Screen to Identify Activators of CRE-BLA: S1P2 Purchased Analogues | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid856 | Counterscreen for S1P2 Antagonists: Dose Response Cell-Based Screen to Identify Antagonists of CRE-BLA | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1470 | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist NMS binding at M1 | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/28/11 |
| aid1323 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 2 (SRC-2) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1331 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 3 (SRC-3) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1534 | Dose response biochemical high throughput screening assay for inhibitors of the p97 ATPase | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1399 | Dose response cell-based assay to measure STAT3 inhibition | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1518 | Dose response cell-based high throughput screening assay for antagonists of the Sphingosine 1-Phosphate Receptor 3 (S1P3) | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1562 | Dose response cell-based high-throughput screening assay for agonists of the transient receptor potential channel ML3 (TRPML3) | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1538 | Dose response cell-based high-throughput screening assay for agonists of the transient receptor potential channel N1 (TRPN1) | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1522 | Dose response cell-based high-throughput screening assay to measure PERK inhibition | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1411 | Dose response counterscreen assay for STAT3 inhibitors: cell-based high throughput assay to measure STAT1 inhibition | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1409 | Dose response counterscreen for STAT1 inhibitors: cell-based high throughput assay to measure STAT3 inhibition | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1221 | Estrogen Receptor (beta) binding: Dose Response of Primary Screen Assay | NMMLSC | 05/28/11 |
| aid1342 | Fluorescence polarization assay for PKD inhibitiors-interference assay-57K HTS campaign | University of Pittsburgh | 05/28/11 |
| aid1077 | Fluorescent secondary assay for dose-response confirmation of chemical inhibitors of HePTP | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1632 | HTS assay for inhibitors of Trypanosoma brucei hexokinase 1: IC50 determinations | University of Pittsburgh | 05/28/11 |
| aid1193 | In Vitro Hsc70 Dose Response Fluorescence Polarization Assay | Sanford-Burnham Center for Chemical Genomics | 05/28/11 |
| aid1544 | Luminescence counterscreen assay for p97 inhibitors: Dose response biochemical high throughput screening assay to identify inhibitors of the C522A mutant p97 ATPase. | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1629 | Luminescence counterscreen assay for p97 inhibitors: dose response biochemical high throughput screening assay to identify inhibitors of the C522A mutant p97 ATPase: synthesized compounds. | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid1512 | Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase confirmation | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1330 | Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-W. | NMMLSC | 05/28/11 |
| aid1340 | Multiplexed dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac wildtype | NMMLSC | 05/28/11 |
| aid1327 | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-B protein. | NMMLSC | 05/28/11 |
| aid1324 | Profiling Assay to determine GST-GSH interactions in multiplex bead-based assays (HPSMTB buffer) | NMMLSC | 05/28/11 |
| aid1056 | SAR analysis of an In Vitro TNAP Dose Response Luminescent Assay | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1666 | SAR assay for compounds that inhibit PHOSPHO1 | Burnham Center for Chemical Genomics | 05/28/11 |
| aid1028 | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC - Secondary Assay | SRMLSC | 05/28/11 |
| aid1641 | TR-FRET counterscreen for FAK inhibitors: dose-response biochemical high throughput screening assay to identify inhibitors of Proline-rich tyrosine kinase 2 (Pyk2) | The Scripps Research Institute Molecular Screening Center | 05/28/11 |
| aid689 | Colorimetric assay for HTS discovery of chemical inhibitors of EphA4 receptor antagonists | Sanford-Burnham Center for Chemical Genomics | 05/27/11 |
| aid779 | Counter Screen for Placental Alkaline Phosphatase-based Assays Positives | Burnham Center for Chemical Genomics | 05/27/11 |
| aid843 | Counter screen for S1P2 Agonists: Dose Response High Throughput Cell-Based Screen to Identify Activators of CRE-BLA | The Scripps Research Institute Molecular Screening Center | 05/27/11 |
| aid842 | Dose response biochemical assay to identify inhibitors of the HIV Rev - RRE RNA interaction (disruption of protein-RNA interaction) | The Scripps Research Institute Molecular Screening Center | 05/27/11 |
| aid852 | Factor XIIa 1536 HTS Dose Response Confirmation | PCMD | 05/27/11 |
| aid844 | Identification of Molecular Probes that Activate MRP-1 - Dose Response | SRMLSC | 05/27/11 |
| aid518 | TNAP luminescent HTS assay | Burnham Center for Chemical Genomics | 05/27/11 |
| aid1744 | Discovery of novel allosteric modulators of the M1 muscarinic receptor: Agonist Activity against Muscarinic Panel | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/25/11 |
| aid1734 | Identification of Novel Modulators of Cl- dependent Transport Process via HTS: Rubidium Flux | Vanderbilt Screening Center for GPCRs, Ion Channels and Transporters | 05/25/11 |
| aid1749 | SAR analysis of Antagonists of IAP-family anti-apoptotic proteins | Burnham Center for Chemical Genomics | 05/25/11 |
| aid1750 | SAR analysis of Antagonists of XIAP-Bir3 domain of IAP-family anti-apoptotic proteins | Burnham Center for Chemical Genomics | 05/25/11 |
| aid1755 | SAR analysis of compounds that potentiate TRAIL-induced apoptosis in MDA-MB-435 cells. | Burnham Center for Chemical Genomics | 05/25/11 |
| aid1752 | SAR analysis of compounds that potentiate TRAIL-induced apoptosis in PPC-1 cells. | Burnham Center for Chemical Genomics | 05/25/11 |
| aid1378 | AKT counterscreen of confirmed PKD inhibitors-57K library | University of Pittsburgh | 05/21/11 |
| aid1380 | CDK7 counterscreen of confirmed PKD inhibitors-57K library addition | University of Pittsburgh | 05/21/11 |
| aid1449 | Chemical Antagonists of IAP-family anti-apoptotic proteins confirmation | Burnham Center for Chemical Genomics | 05/21/11 |
| aid1414 | Counterscreen assay for inhibitors of Wee1 degradation: dose response cell-based assay to identify inhibitors of cyclin B degradation | The Scripps Research Institute Molecular Screening Center | 05/21/11 |
| aid1412 | Dose Response Cell-based Assay for Inhibitors of Wee1 Degradation | The Scripps Research Institute Molecular Screening Center | 05/21/11 |
| aid1396 | Dose response cell-based assay to measure STAT1 inhibition | The Scripps Research Institute Molecular Screening Center | 05/21/11 |
| aid1398 | Dose response cell-based assay to measure STAT3 activation | The Scripps Research Institute Molecular Screening Center | 05/21/11 |
| aid1406 | Dose response counterscreen assay for STAT3 activators: cell-based high throughput assay to measure STAT1 activation | The Scripps Research Institute Molecular Screening Center | 05/21/11 |
| aid1404 | Dose response counterscreen for STAT1 activators: cell-based high throughput assay to measure STAT3 activation | The Scripps Research Institute Molecular Screening Center | 05/21/11 |
| aid1394 | E3 Ligase dose-response_384 | PCMD | 05/21/11 |
| aid1383 | PLK1 counterscreening assay for identified PKD inhibitors | University of Pittsburgh | 05/21/11 |
| aid1392 | RNA polymerase SAR | PCMD | 05/21/11 |
| aid1450 | SAR assay for compounds activating TNAP in the absence of phosphate acceptor performed in a luminescent assay | Burnham Center for Chemical Genomics | 05/21/11 |
| aid1319 | Dose response biochemical High Throughput Screening assay for agonists of the steroid receptor coactivator 1 (SRC-1) recruitment by the peroxisome proliferator-activated receptor gamma (PPARgamma) | The Scripps Research Institute Molecular Screening Center | 05/20/11 |
| aid1284 | Dose response biochemical screening assay for inhibitors of c-Jun N-Terminal Kinase 3 (JNK3) | The Scripps Research Institute Molecular Screening Center | 05/20/11 |
| aid1268 | Dose response cell-based high throughput screening assay to identify enhancers of beta-glucosidase activity | The Scripps Research Institute Molecular Screening Center | 05/20/11 |
| aid1277 | Dose response cell-based screening assay for antagonists of neuropeptide Y receptor Y1 (NPY-Y1) | The Scripps Research Institute Molecular Screening Center | 05/20/11 |
| aid1278 | Dose response counterscreen assay for neuropeptide Y receptor Y1 (NPY-Y1): Cell-based high throughput assay to measure NPY-Y2 antagonism | The Scripps Research Institute Molecular Screening Center | 05/20/11 |
| aid1279 | Dose response counterscreen for neuropeptide Y receptor Y2 (NPY-Y2): Cell-based high throughput assay to measure NPY-Y1 antagonism | The Scripps Research Institute Molecular Screening Center | 05/20/11 |
| aid1333 | Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Cdc42 activated mutant | NMMLSC | 05/20/11 |
| aid1337 | Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rab2 wildtype | NMMLSC | 05/20/11 |
| aid1339 | Multiplex dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Rac activated mutant | NMMLSC | 05/20/11 |
| aid1329 | Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Mcl-1. | NMMLSC | 05/20/11 |
| aid1335 | Multiplexed dose response to identify specific small molecule inhibitors of Ras and Ras-related GTPases specifically Ras wildtype | NMMLSC | 05/20/11 |
| aid1328 | Multiplexed high-throughput screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-2 | NMMLSC | 05/20/11 |
| aid1261 | YopH - IC50 determinations (10 point dose range) | University of Pittsburgh | 05/20/11 |
| aid1003 | Confirmation Cuvette-Based Assay for Inhibitors of AmpC Beta-Lactamase (assay with detergent) | NCGC | 05/17/11 |
| aid1244 | Counter Screen for TR3-Based Bcl-B Inhibitors: Fluorescence Polarization Bcl-B/FITC-Bim-BH3 Assay | Sanford-Burnham Center for Chemical Genomics | 05/17/11 |
| aid1050 | Dose Response cell-based high-throughput screening assay to identify agonists of galanin receptor 2 (GALR2) | The Scripps Research Institute Molecular Screening Center | 05/17/11 |
| aid1225 | Dose Response cell-based high-throughput screening assay to identify antagonists of galanin receptor 2 (GALR2) | The Scripps Research Institute Molecular Screening Center | 05/17/11 |
| aid1228 | Dose response counterscreen for agonists of galanin receptor 2 (GalR2): a cell-based high-throughput screening assay for activators of beta-lactamase activity | The Scripps Research Institute Molecular Screening Center | 05/17/11 |
| aid1238 | Dose response counterscreen for antagonists of galanin receptor 2 (GalR2): a cell-based high-throughput screening assay for inhibitors of beta-lactamase activity | The Scripps Research Institute Molecular Screening Center | 05/17/11 |
| aid1223 | Estrogen Receptor (alpha) binding: Dose Response of Primary Screen Assay | NMMLSC | 05/17/11 |
| aid1079 | Estrogen Receptor-alpha Coactivator Binding Inhibitors ELISA Secondary Assay | Emory University | 05/17/11 |
| aid1243 | Fluorescence Polarization Dose Response Assay for TR3-Based Bcl-B Inhibitors | Sanford-Burnham Center for Chemical Genomics | 05/17/11 |
| aid1227 | GAPDH Dose Response Colorimetric Assay | Sanford-Burnham Center for Chemical Genomics | 05/17/11 |
| aid1233 | High Throughput Screen to Identify Compounds that Inhibit Class II HMG-CoA Reductases - Confirmatory Screen | SRMLSC | 05/17/11 |
| aid1070 | In Vitro Bfl-1 Dose Response Fluorescence Polarization Assay for SAR Study | Sanford-Burnham Center for Chemical Genomics | 05/17/11 |
| aid1072 | In Vitro Hsp70 Dose Response Fluorescence Polarization Assay for SAR Study | Burnham Center for Chemical Genomics | 05/17/11 |
| aid1017 | Luminescent assay for identification of inhibitors of human intestinal alkaline phosphatase | Sanford-Burnham Center for Chemical Genomics | 05/17/11 |
| aid1052 | MKP-3 in vitro secondary assay for identification of irreversible and slow-binding inhibitors | Burnham Center for Chemical Genomics | 05/17/11 |
| aid1058 | SMAD Transcription Factor Inhibitors Secondary Dose Response Confirmation | Emory University | 05/17/11 |
| aid1026 | sEH_DR_Inh_Infinite200_Fluorescence_01072008 | Columbia University Molecular Screening Center | 05/17/11 |
| aid832 | Cathepsin G dose-response confirmation | PCMD | 05/12/11 |
| aid831 | Cathepsin S dose-response confirmation | PCMD | 05/12/11 |
| aid876 | Concentration Response Redox Cycling H2O2 Generation assay to characterize small molecule inhibitors identified in the Polo box domain (PBD) of Plk1 Primary HTS. | University of Pittsburgh | 05/12/11 |
| aid877 | Concentration Response fluorescence polarization-based assay to confirm small molecule inhibitors identified in the Polo box domain (PBD) of Plk1 Primary HTS. | University of Pittsburgh | 05/12/11 |
| aid854 | Dose Response Cell Based Assay for Agonists of the S1P2 Receptor | The Scripps Research Institute Molecular Screening Center | 05/12/11 |
| aid872 | Dose Response Cell Based Assay for Agonists of the S1P2 Receptor of Purchased Analogues | The Scripps Research Institute Molecular Screening Center | 05/12/11 |
| aid851 | Dose Response Cell Based Assay for Antagonists of the S1P2 Receptor | The Scripps Research Institute Molecular Screening Center | 05/12/11 |
| aid835 | Dose-response biochemical assay for antagonists of the interaction between the Eph receptor B4 (EphB4) and its ligand ephrin-B2 via TNYL-RAW peptide | The Scripps Research Institute Molecular Screening Center | 05/12/11 |
| aid838 | Mycobacterium tuberculosis Pantothenate Synthetase Secondary Assay | SRMLSC | 05/12/11 |
| aid820 | Cathepsin B dose-response confirmation | PCMD | 05/11/11 |
| aid825 | Cathepsin L dose-response confirmation | PCMD | 05/11/11 |
| aid829 | Complement C1s ELISA | PCMD | 05/11/11 |
| aid787 | Complement factor C1s IC50 from mixture screen | PCMD | 05/11/11 |
| aid810 | Dose-response biochemical assay for inhibitors of Focal Adhesion Kinase (FAK) | The Scripps Research Institute Molecular Screening Center | 05/11/11 |
| aid826 | RNA polymerase dose-response confirmation | PCMD | 05/11/11 |
| aid786 | TR-FRET secondary assay for HTS discovery of chemical inhibitors of Hsp70 | Burnham Center for Chemical Genomics | 05/11/11 |
| aid714 | BAP1 Enzyme inhibitors Dose Response Confirmation | Emory University | 05/06/11 |
| aid754 | Cell-based secondary assay for identifying Hsp90 inhibitors that degrade Hsp90 client protein Her2 | Emory University | 05/06/11 |
| aid769 | Dose response biochemical assay for autofluorescent inhibitors of Matrix Metalloproteinase 13 (MMP13) activity | The Scripps Research Institute Molecular Screening Center | 05/06/11 |
| aid735 | Dose-response biochemical assay for inhibitors of Matrix Metalloproteinase 13 (MMP13) activity | The Scripps Research Institute Molecular Screening Center | 05/06/11 |
| aid713 | Estrogen Receptor-alpha Coactivator Binding Inhibitors Dose Response Confirmation | Emory University | 05/06/11 |
| aid737 | Estrogen Receptor-alpha Coactivator Binding Potentiators Dose Response Confirmation | Emory University | 05/06/11 |
| aid716 | Factor XIIa Dose Response Confirmation | PCMD | 05/06/11 |
| aid724 | Formylpeptide Receptor (FPR) Ligand Structure Activity Relationship (SAR) Analysis : Dose Response Assay | NMMLSC | 05/06/11 |
| aid723 | Formylpeptide Receptor (FPR) Ligand Structure Activity Relationship (SAR) Analysis : Dose Response Assay Counterscreen Against Formyl Peptide Receptor-Like-1 (FPRL1) | NMMLSC | 05/06/11 |
| aid766 | Formylpeptide Receptor (FPRL1) Ligand Structure Activity Relationship (SAR) Analysis : Dose Response Assay | NMMLSC | 05/06/11 |
| aid762 | Formylpeptide Receptor (FPRL1) Ligand Structure Activity Relationship (SAR) Analysis : FPR Dose Response Counterscreen Assay | NMMLSC | 05/06/11 |
| aid748 | High Throughput Fluorescence Polarization Screen for Bcl-B Phenotype Converters | Burnham Center for Chemical Genomics | 05/06/11 |
| aid730 | S1P3 Dose Response Assay Counterscreen for 5-Hydroxytryptamine(Serotonin) Receptor Subtype 1E Agonists | The Scripps Research Institute Molecular Screening Center | 05/06/11 |
| aid776 | S1P3 Dose Response Assay Counterscreen for 5-Hydroxytryptamine(Serotonin) Receptor Subtype 1E Antagonists | The Scripps Research Institute Molecular Screening Center | 05/06/11 |
| aid715 | SMAD Transcription Factor Inhibitors Dose Response Confirmation | Emory University | 05/06/11 |
| aid711 | 14-3-3 protein interaction modulators Dose Response Confirmation | Emory University | 05/05/11 |
| aid695 | Counterscreen for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA): A cell-based dose-response assay for inhibition of the Steroidogenic Factor 1 (SF-1) | The Scripps Research Institute Molecular Screening Center | 05/04/11 |
| aid692 | Dose-response cell-based assay for activators of the nuclear receptor Steroidogenic Factor 1 (SF-1) | The Scripps Research Institute Molecular Screening Center | 05/04/11 |
| aid569 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase HTS Dose Response Confirmation Assay | University of Pittsburgh | 04/30/11 |
| aid650 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response Reproducibility Assay | University of Pittsburgh | 04/30/11 |
| aid649 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in 25 mM DTT | University of Pittsburgh | 04/30/11 |
| aid669 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in 25 mM DTT and Catalase. | University of Pittsburgh | 04/30/11 |
| aid670 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in the presence of Beta-Mercaptoethanol. | University of Pittsburgh | 04/30/11 |
| aid668 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in the presence of Catalase. | University of Pittsburgh | 04/30/11 |
| aid671 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment Dose Response assay in the presence of Glutathione. | University of Pittsburgh | 04/30/11 |
| aid674 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment: MKP-1 Dose Response Selectivity comparison. | University of Pittsburgh | 04/30/11 |
| aid673 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Probe Assessment: MKP-3 Dose Response Selectivity comparison. | University of Pittsburgh | 04/30/11 |
| aid675 | Counterscreen for activators of the nuclear receptor Steroidogenic Factor 1 (SF-1): A cell-based dose-response assay for inhibition of the RAR-related orphan receptor A (RORA) | The Scripps Research Institute Molecular Screening Center | 04/30/11 |
| aid611 | Counterscreen for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA): A cell-based dose-response assay for inhibition of the Steroidogenic Factor 1 (SF-1) | The Scripps Research Institute Molecular Screening Center | 04/30/11 |
| aid599 | Counterscreen for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1): A cell-based dose-response assay for inhibition of the RAR-related orphan receptor A (RORA) | The Scripps Research Institute Molecular Screening Center | 04/30/11 |
| aid644 | Dose-response biochemical assay of inhibitors of Rho kinase 2 (Rock2) | The Scripps Research Institute Molecular Screening Center | 04/30/11 |
| aid681 | Dose-response cell-based assay for activators of the Retinoic Acid Receptor-related orphan receptor A (RORA) | The Scripps Research Institute Molecular Screening Center | 04/30/11 |
| aid610 | Dose-response cell-based assay for inhibitors of the Retinoic Acid Receptor-related orphan receptor A (RORA) | The Scripps Research Institute Molecular Screening Center | 04/30/11 |
| aid600 | Dose-response cell-based assay for inhibitors of the nuclear receptor Steroidogenic Factor 1 (SF-1) | The Scripps Research Institute Molecular Screening Center | 04/30/11 |
| aid679 | Factor XIa Dose Response Confirmation | PCMD | 04/30/11 |
| aid606 | HTS for LYP Inhibitors-an Autoimmunity Target - Primary screen | Columbia University Molecular Screening Center | 04/30/11 |
| aid562 | In vitro MKP-1 Phosphatase Dose Response Active/Probe Assessment Assay - Effects of Catalase | University of Pittsburgh | 04/30/11 |
| aid558 | In vitro MKP-1 Phosphatase Dose Response Active/Probe Assessment Assay - Effects of DTT | University of Pittsburgh | 04/30/11 |
| aid563 | In vitro MKP-1 Phosphatase Dose Response Active/Probe Assessment Assay - Reproducibility testing | University of Pittsburgh | 04/30/11 |
| aid564 | In vitro MKP-3 Phosphatase Dose Response Active/Probe Assessment Assay - Effects of Catalase | University of Pittsburgh | 04/30/11 |
| aid566 | In vitro MKP-3 Phosphatase Dose Response Active/Probe Assessment Assay - Reproducibility testing | University of Pittsburgh | 04/30/11 |
| aid690 | Luminescent assay for HTS discovery of chemical inhibitors of placental alkaline phosphatase | Burnham Center for Chemical Genomics | 04/30/11 |
| aid676 | MKP-1 Dual Specificity Protein Tyrosine Phosphatase Probe Assessment: Cdc25B Dose Response Selectivity Assay | University of Pittsburgh | 04/30/11 |
| aid557 | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - MK Dose Response | SRMLSC | 04/30/11 |
| aid621 | TR-FRET secondary assay for HTS discovery of chemical inhibitors of anti-apoptotic protein Bfl-1 | Sanford-Burnham Center for Chemical Genomics | 04/30/11 |
| aid653 | West Nile Virus NS2bNS3 Proteinase Inhibitor Dose Response Confirmation. | University of Pittsburgh | 04/30/11 |
| aid523 | Cathepsin B Inhibitor Series SAR Study | PCMD | 04/29/11 |
| aid486 | Clearance of Mutant Huntingtin Protein - Confirmatory screen | Columbia University Molecular Screening Center | 04/29/11 |
| aid519 | Dose Response Assay for Formylpeptide Receptor (FPR) Ligands and Dose Response Counter-Screen Assay for Formylpeptide-Like-1 (FPRL1) Ligands | NMMLSC | 04/29/11 |
| aid520 | Dose Response Assay for Formylpeptide Receptor-Like-1 (FPRL1) Ligands and Dose Response Counter-Screen Assay for Formylpeptide Receptor (FPR) Ligands | NMMLSC | 04/29/11 |
| aid484 | Dose Response Assay for S1P3 Antagonists | The Scripps Research Institute Molecular Screening Center | 04/29/11 |
| aid468 | Dose Response Assays for S1P1 Agonists and Agonism Potentiators - Agonist Assay 60K MLSMR | The Scripps Research Institute Molecular Screening Center | 04/29/11 |
| aid548 | Dose-response biochemical assay for inhibitors of protein kinase A (PKA) activity | The Scripps Research Institute Molecular Screening Center | 04/29/11 |
| aid553 | In vitro MKP-3 Phosphatase Dose Response Hit/Probe Assessment Assay | University of Pittsburgh | 04/29/11 |
| aid550 | Screening for Inhibitors of the Mevalonate Pathway in Streptococcus Pneumoniae - DPM-DC Dose Response | SRMLSC | 04/29/11 |
| aid443 | Cdc25B Catalytic Domain Protein Tyrosine Phosphatase Dose Response Confirmation and Secondary Selectivity/Specificity Assay | University of Pittsburgh | 04/28/11 |
| aid467 | Dose Response Assays for S1P1 Agonists and Agonism Potentiators - Parental Cell Line Counter Screen 60K MLSMR | The Scripps Research Institute Molecular Screening Center | 04/28/11 |
| aid466 | Dose Response Assays for S1P1 Agonists and Agonism Potentiators - Potentiator Assay 60K MLSMR | The Scripps Research Institute Molecular Screening Center | 04/28/11 |
| aid442 | In vitro MKP-1 Phosphatase Dose Response Confirmation and Secondary Selectivity/Specificity Assay | University of Pittsburgh | 04/28/11 |
| aid452 | In vitro MKP-3 Phosphatase Dose Response Confirmation and Secondary Selectivity/Selectivity Assay | University of Pittsburgh | 04/28/11 |
| aid375 | Mycobacterium tuberculosis Pantothenate Synthetase Assay | SRMLSC | 04/28/11 |
| aid439 | S1P3 Agonist Dose-Response Potency Assay | The Scripps Research Institute Molecular Screening Center | 04/28/11 |
| aid1433 | Kinase Inhibitor Selectivity Profiling Assay | Ambit Biosciences | 04/23/11 |
| aid830 | Cathepsin B mixture HTS dose-response confirmation | PCMD | 12/17/09 |
| aid579 | In vitro MKP-1 Phosphatase Dose Response SAR Support Assay | CC_PMLSC | 12/17/09 |
| aid551 | In vitro MKP-1 Phosphatase HTS Dose Response Confirmation Assay | University of Pittsburgh | 12/17/09 |
| aid652 | HIV-1 RT-RNase H MLSCN MH077605 Probe Assessment: Dose response Assay | University of Pittsburgh | 11/24/09 |
| aid432 | HTS discovery of chemical inhibitors of anti-apoptotic protein Bfl-1 | Burnham Center for Chemical Genomics | 11/24/09 |
| aid1220 | HTS identification of compounds inhibiting phosphomannose isomerase (PMI) via a fluorescence intensity assay using a high concentration of mannose 6-phosphate | Burnham Center for Chemical Genomics | 11/24/09 |
| aid728 | Factor XIIa Dose Response Confirmation from Single Well HTS | PCMD | 11/09/09 |
| aid1215 | Thrombin 1536 HTS Dose Response Confirmation | PCMD | 11/09/09 |
| aid846 | Factor XIa 1536 HTS Dose Response Confirmation | PCMD | 10/26/09 |
| aid721 | Factor XIa Dose Response Confirmation from Single Well Screen | PCMD | 10/26/09 |
| aid1320 | Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bfl-1. | NMMLSC | 10/26/09 |
| aid1408 | Fluorescence polarization assay for PKD inhibitiors-IC50 determinations | University of Pittsburgh | 10/09/09 |
| aid1322 | Multiplexed dose response screen for small molecule regulators of Bcl-2 family protein interactions, specifically Bim-Bcl-XL. | NMMLSC | 10/09/09 |
| aid712 | Tumor Hsp90 Inhibitors Dose Response Confirmation | Emory University | 10/09/09 |
| aid583 | High Throughput Screening Assay for Hsp70 Inhibitors | Burnham Center for Chemical Genomics | 09/25/09 |
| aid1055 | In Vitro MKP-3 Dose Response Assay for SAR Study | Burnham Center for Chemical Genomics | 09/25/09 |
| aid1516 | Counterscreen assay for S1P3 antagonists: Dose response cell-based high throughput screening assay to identify antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | The Scripps Research Institute Molecular Screening Center | 09/05/09 |
| aid749 | Dose Response Cell Based Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | The Scripps Research Institute Molecular Screening Center | 09/05/09 |
| aid726 | Dose Response Cell Based High Throughput Screening Assay for Agonists of the 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | The Scripps Research Institute Molecular Screening Center | 09/05/09 |
| aid613 | Dose Response Assay for 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1a (5HT1a) Agonists | The Scripps Research Institute Molecular Screening Center | 08/14/09 |
| aid755 | Dose Response Cell Based Assay for Antagonists of the 5-Hydroxytryptamine Receptor Subtype 1A (5HT1A) | The Scripps Research Institute Molecular Screening Center | 08/14/09 |
| aid718 | Dose Response assay for agonists of 5-Hydroxytryptamine (Serotonin) Receptor Subtype 1A (5HT1A) | The Scripps Research Institute Molecular Screening Center | 08/14/09 |
| aid1560 | Confirmation of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a fluorescence resonance energy transfer (FRET) assay | Burnham Center for Chemical Genomics | 07/24/09 |
| aid1550 | Confirmation of compounds inhibiting the binding between the RUNX1 Runt domain and CBFbeta-SMMHC via a time resolved fluorescence resonance energy transfer (TR-FRET) assay. | Burnham Center for Chemical Genomics | 07/24/09 |
| aid1434 | uHTS identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFbeta-SMMHC via a fluorescence resonance energy transfer (FRET) assay. | Burnham Center for Chemical Genomics | 07/24/09 |
| aid1438 | Identification of compounds inhibiting the binding between the RUNX1 Runt domain and CBFb-SMMHC via a time resolved fluorescence resonance energy transfer (TR-FRET) assay. | Burnham Center for Chemical Genomics | 06/18/09 |