Compile Data Set for Download or QSAR
Found 62 with Last Name = 'skepper' and Initial = 'ck'
TargetDNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50197073(3-amino-7-((R)-3-((S)-1-aminoethyl)pyrrolidin-1-yl...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MQSPubMed
TargetDNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50542206(CHEMBL4640061)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MQSPubMed
TargetDNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM21690(1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,...)copy SMILEScopy InChI
Affinity DataIC50: 490nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MQSPubMedDrugBank
TargetDNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50542207(CHEMBL4634552)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+3nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MQSPubMed
LigandPNGBDBM50566539(CHEMBL4860033)copy SMILES
Affinity DataIC50: 2.70E+3nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
TargetDNA gyrase subunit A/B(Escherichia coli (strain K12))
Novartis Institutes for BioMedical Research

Curated by ChEMBL
LigandPNGBDBM50542205(CHEMBL4643875)copy SMILEScopy InChI
Affinity DataIC50: 2.91E+3nMAssay Description:Inhibition of recombinant full-length C-terminal His6-tagged Escherichia coli DNA gyrase AB supercoiling activity using relaxed DNA as substrate prei...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MQSPubMed
LigandPNGBDBM50566543(CHEMBL4864037)copy SMILES
Affinity DataIC50: 8.00E+3nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566541(CHEMBL4867915)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566538(CHEMBL4875315)copy SMILES
Affinity DataIC50: 1.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
TargetBifunctional coenzyme A synthase(Homo sapiens)
Novartis Institutes for BioMedical Research , 5300 Chiron Way , Emeryville , California 94608 , United States.

Curated by ChEMBL
LigandPNGBDBM50263238(CHEMBL4102651)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human PPATMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S46VFKPubMed
LigandPNGBDBM50566542(CHEMBL4878164)copy SMILES
Affinity DataIC50: 1.20E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566546(CHEMBL4875871)copy SMILES
Affinity DataIC50: 1.30E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566544(CHEMBL4852170)copy SMILES
Affinity DataIC50: 1.70E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566545(CHEMBL4861495)copy SMILES
Affinity DataIC50: 1.80E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566510(CHEMBL4860105)copy SMILES
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566540(CHEMBL4877922)copy SMILES
Affinity DataIC50: 2.90E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566535(CHEMBL4860370)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566519(CHEMBL4868731)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566517(CHEMBL4873798)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566514(CHEMBL4865462)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566513(CHEMBL4869164)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566549(CHEMBL4856534)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566547(CHEMBL4869998)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566548(CHEMBL4861063)copy SMILES
Affinity DataIC50: 3.00E+4nMAssay Description:Displacement of [3H]-dofetilide from human ERG after 60 mins by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566524(CHEMBL4867992)copy SMILES
Affinity DataIC50: 4.20E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50542206(CHEMBL4640061)copy SMILEScopy InChI
Affinity DataIC50: 4.88E+4nMAssay Description:Inhibition of human ERG expressed in HEK293 cells measured after 10 mins by manual patch clamp electrophysiology methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MQSPubMed
LigandPNGBDBM50542206(CHEMBL4640061)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by manual patch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
TargetSodium channel protein type 5 subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50542205(CHEMBL4643875)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of human Nav1.5 expressed in HEK293 cells by IonWorks patch clamp electrophysiology methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
TargetSodium channel protein type 5 subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50542206(CHEMBL4640061)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of human Nav1.5 expressed in HEK293 cells by IonWorks patch clamp electrophysiology methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566522(CHEMBL4847738)copy SMILES
Affinity DataIC50: 9.00E+4nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
TargetSodium channel protein type 5 subunit alpha(Homo sapiens (Human))TBA
LigandPNGBDBM50566512(CHEMBL4857241)copy SMILES
Affinity DataIC50: 9.20E+4nMAssay Description:Inhibition of human Nav1.5 expressed in HEK293 cells by IonWorks patch clamp electrophysiology methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566511(CHEMBL4846404)copy SMILES
Affinity DataIC50: 1.09E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50542207(CHEMBL4634552)copy SMILEScopy InChI
Affinity DataIC50: 1.14E+5nMAssay Description:Inhibition of human ERG expressed in CHOK1 cells measured for 10 mins by QPatch automated patch-clamp assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2MQSPubMed
LigandPNGBDBM50566536(CHEMBL4633030)copy SMILES
Affinity DataIC50: 1.14E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by long incubation protocol based Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566523(CHEMBL4851838)copy SMILES
Affinity DataIC50: 1.26E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566537(CHEMBL4874636)copy SMILES
Affinity DataIC50: 1.27E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by long incubation protocol based Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50366824(Avelox | MOXIFLOXACIN | Moxifl-oxacin)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+5nMAssay Description:Inhibition of human ERG expressed in CHO cells by whole cell patch-clamp methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566512(CHEMBL4857241)copy SMILES
Affinity DataIC50: 1.36E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566521(CHEMBL4855694)copy SMILES
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566513(CHEMBL4869164)copy SMILES
Affinity DataIC50: 1.88E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566520(CHEMBL4849541)copy SMILES
Affinity DataIC50: 2.11E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50542205(CHEMBL4643875)copy SMILEScopy InChI
Affinity DataIC50: 2.14E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566514(CHEMBL4865462)copy SMILES
Affinity DataIC50: 2.93E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566518(CHEMBL4855895)copy SMILES
Affinity DataIC50: 2.97E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566534(CHEMBL4869317)copy SMILES
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566533(CHEMBL4866375)copy SMILES
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566532(CHEMBL4852578)copy SMILES
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566531(CHEMBL4860997)copy SMILES
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566529(CHEMBL4861982)copy SMILES
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
LigandPNGBDBM50566528(CHEMBL4855299)copy SMILES
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of human ERG expressed in CHO-K1 cells by Qpatch clamp methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0S2GPubMed
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