Compile Data Set for Download or QSAR
Found 215 with Last Name = 'mueller' and Initial = 'a'
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010495(Acetyl-Ser-Leu-Asn-Phe-[CH(OH)CH2N]Pro-Ile-Val-OMe...)copy SMILEScopy InChI
Affinity DataKi:  0.600nMAssay Description:In vitro binding affinity of the compound against HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010497(Acetyl-Ser-Leu-Asn-Phe-[S]-[CH(OH)CH2N]Pro-Ile-Val...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010497(Acetyl-Ser-Leu-Asn-Phe-[S]-[CH(OH)CH2N]Pro-Ile-Val...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023523(2,2-Dimethyl-propionic acid 2-[2,4-bis-(2,2-dimeth...)copy SMILEScopy InChI
Affinity DataKi:  68nMAssay Description:Binding affinity towards human leukocyte elastase at 10e-8 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023518(2,4-Bis-(2,2-dimethyl-propionyloxy)-benzoic acid 5...)copy SMILEScopy InChI
Affinity DataKi:  70nMAssay Description:Binding affinity towards human leukocyte elastase at 10e-7 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023545(2,2-Dimethyl-propionic acid 4-[4-(2,2-dimethyl-pro...)copy SMILEScopy InChI
Affinity DataKi:  71nMAssay Description:Binding affinity towards human leukocyte elastase at 10e-8 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023542(2,2-Dimethyl-propionic acid 4-[4-(2,2-dimethyl-pro...)copy SMILEScopy InChI
Affinity DataKi:  200nMAssay Description:Inhibitory activity against human leukocyte elastase at 10e-7 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011680(CHEMBL3351098 | Qua-Asn-Phe-HEA(S)-Pro-Ile-Phe-OMe)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM486((2S)-N-[(2S,3R)-4-[(tert-butylcarbamoyl)(3-methylb...)copy SMILEScopy InChI
Affinity DataIC50: 3nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM490((2S)-N-[(2S,3R)-4-[benzyl(tert-butylcarbamoyl)amin...)copy SMILEScopy InChI
Affinity DataIC50: 3nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586984(CHEMBL5084771)copy SMILES
Affinity DataIC50: 3.10nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586985(CHEMBL5082735)copy SMILES
Affinity DataIC50: 3.5nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011684(CHEMBL3350878 | Cbz-Asn-Phe-HEA(S)-Pro-Ile-Phe-OMe)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586972(CHEMBL5088921)copy SMILES
Affinity DataIC50: 4.90nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM488((2S)-N-[(2S,3R)-4-[(tert-butylcarbamoyl)(cyclohexy...)copy SMILEScopy InChI
Affinity DataIC50: 5nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM483((2S)-N-[(2S,3R)-4-[(tert-butylcarbamoyl)(2-methylp...)copy SMILEScopy InChI
Affinity DataIC50: 6nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
LigandPNGBDBM50586985(CHEMBL5082735)copy SMILES
Affinity DataIC50: 7.80nMAssay Description:Displacement of [18F]-FEH from MAO-A in mouse brain homogenate incubated for 60 mins by imaging analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010495(Acetyl-Ser-Leu-Asn-Phe-[CH(OH)CH2N]Pro-Ile-Val-OMe...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:In vitro binding affinity of the compound against HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM146127(US8957068, 162)copy SMILEScopy InChI
Affinity DataIC50: 10nMMore data for this Ligand-Target Pair
In DepthDetails
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM485((Hydroxyethyl)urea Isostere deriv. 13 | benzyl N-[...)copy SMILEScopy InChI
Affinity DataIC50: 13nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011687(Ac-Ser-Leu-Asn-Phe-HEA(R)-Pro-O-terbutyl | CHEMBL3...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011682(Ac-Ser-Leu-Asn-Phe-HEA(S)-Pro-O-terbutyl | BDBM504...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM50279397(CHEMBL4169151 | US11311527, Cpd ID IDH889 | US1137...)copy SMILEScopy InChI
Affinity DataIC50: 14nMMore data for this Ligand-Target Pair
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586975(CHEMBL5081662)copy SMILES
Affinity DataIC50: 16nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50011688(Boc-Asn-Phe-HEA(R)-Pro-Ile-Val-OMe | CHEMBL3349554)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM146127(US8957068, 162)copy SMILEScopy InChI
Affinity DataIC50: 17nMMore data for this Ligand-Target Pair
In DepthDetails
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586986(CHEMBL5091624)copy SMILES
Affinity DataIC50: 18nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM494((2S)-N-[(2S,3R)-4-[(tert-butylcarbamoyl)(pyridin-4...)copy SMILEScopy InChI
Affinity DataIC50: 19nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM489((Hydroxyethyl)urea Isostere deriv. 17 | benzyl N-[...)copy SMILEScopy InChI
Affinity DataIC50: 19nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM50279397(CHEMBL4169151 | US11311527, Cpd ID IDH889 | US1137...)copy SMILEScopy InChI
Affinity DataIC50: 20nMMore data for this Ligand-Target Pair
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM146127(US8957068, 162)copy SMILEScopy InChI
Affinity DataIC50: 22nMMore data for this Ligand-Target Pair
In DepthDetails
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023523(2,2-Dimethyl-propionic acid 2-[2,4-bis-(2,2-dimeth...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Binding affinity towards human leukocyte elastase at 10e-7 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023518(2,4-Bis-(2,2-dimethyl-propionyloxy)-benzoic acid 5...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibitory activity against human leukocyte elastase at 10e-8 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM487((Hydroxyethyl)urea Isostere deriv. 15 | benzyl N-[...)copy SMILEScopy InChI
Affinity DataIC50: 29nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetDimer of Gag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Monsanto Corporate Research

LigandPNGBDBM481((Hydroxyethyl)urea Isostere deriv. 9 | benzyl N-[(...)copy SMILEScopy InChI
Affinity DataIC50: 35nMpH: 6.4 T: 2°CAssay Description:IC50 values for inhibition of recombinant HIV protease were determined using the spectrofluorometric assay, which utilized an intramolecularly quench...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7FTFPubMed
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586979(CHEMBL5084917)copy SMILES
Affinity DataIC50: 36nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
LigandPNGBDBM50586984(CHEMBL5084771)copy SMILES
Affinity DataIC50: 51nMAssay Description:Displacement of [18F]-FEH from MAO-A in mouse brain homogenate incubated for 60 mins by imaging analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50005687(1-[3-(2-Benzyloxycarbonylamino-3-carbamoyl-propion...)copy SMILEScopy InChI
Affinity DataIC50: 51nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measured (exp 2)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023517(2,2-Dimethyl-propionic acid 5-(2,2-dimethyl-propio...)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Inhibitory activity against human leukocyte elastase at 10e-5 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetSqualene synthase(Homo sapiens (Human))
Bayer Pharma AG

Curated by ChEMBL
LigandPNGBDBM50344969(CHEMBL1778340 | [(4R,6S)-8-Chloro-6-(2,3-dimethoxy...)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Inhibition of recombinant squalene synthase assessed as conversion of trans,trans-[1-3H]farnesyl pyrophosphate to [3H]squalene after 10 mins by liqui...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WW7J0XPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010497(Acetyl-Ser-Leu-Asn-Phe-[S]-[CH(OH)CH2N]Pro-Ile-Val...)copy SMILEScopy InChI
Affinity DataIC50: 65nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
University of Wisconsin-Madison

Curated by ChEMBL
LigandPNGBDBM50010497(Acetyl-Ser-Leu-Asn-Phe-[S]-[CH(OH)CH2N]Pro-Ile-Val...)copy SMILEScopy InChI
Affinity DataIC50: 65nMAssay Description:In vitro concentration of the compound required to inhibit 50% activity of HIV protease was measuredMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2057DWMPubMed
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586982(CHEMBL5083649)copy SMILES
Affinity DataIC50: 70nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM50279397(CHEMBL4169151 | US11311527, Cpd ID IDH889 | US1137...)copy SMILEScopy InChI
Affinity DataIC50: 72nMMore data for this Ligand-Target Pair
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023522(CHEMBL9969 | Octadecanoic acid 5-isobutyryloxy-4-o...)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibitory activity against human leukocyte elastase at 10e-8 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM50458784(CHEMBL4216196)copy SMILEScopy InChI
Affinity DataIC50: 81nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetMicrotubule-associated protein tau(Homo sapiens (Human))TBA
LigandPNGBDBM50586973(CHEMBL5077904)copy SMILES
Affinity DataIC50: 82nMAssay Description:Displacement of [3H]PI-2620 from Tau in human brain homogenate incubated for 60 mins by radioligand binding assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC3698PubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023542(2,2-Dimethyl-propionic acid 4-[4-(2,2-dimethyl-pro...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibitory activity against human leukocyte elastase at 10e-8 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
Searle Research and Development

Curated by ChEMBL
LigandPNGBDBM50023550(2,2-Dimethyl-propionic acid 2-benzoyl-5-(2,2-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 84nMAssay Description:Inhibitory activity against human leukocyte elastase at 10e-8 MMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2PC31DJPubMed
TargetIsocitrate dehydrogenase [NADP] cytoplasmic(Homo sapiens (Human))TBA
LigandPNGBDBM50615219(CHEMBL5273829)copy SMILES
Affinity DataIC50: 90nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
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