Compile Data Set for Download or QSAR
Found 38 of ki data for polymerid = 10005,10615,11125,11131,11140,11148,11160,11217,11219,9035
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043760(2-Amino-4-[1-[(carboxy-phenyl-methyl)-carbamoyl]-2...)copy SMILEScopy InChI
Affinity DataKi:  120nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50562986(CHEMBL4757438)copy SMILES
Affinity DataKi:  170nMAssay Description:Time dependent inhibition of GSTP1-1 (unknown origin) assessed as inhibition constant using reduced GSH and CDNB as substrate by spectrophotometric m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27948D3PubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50054198(CHEMBL3310888)copy SMILEScopy InChI
Affinity DataKi:  360nMAssay Description:Competitive inhibition of human GSTA1 activity by double reciprocal Lineweaver-Burk graphMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P625BPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50054196(CHEMBL3310887)copy SMILEScopy InChI
Affinity DataKi:  380nMAssay Description:Competitive inhibition of human GSTA1 activity by double reciprocal Lineweaver-Burk graphMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P625BPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043762(2-Amino-4-{2-benzylsulfanyl-1-[(carboxy-phenyl-met...)copy SMILEScopy InChI
Affinity DataKi:  420nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50173725(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(2-hydrox...)copy SMILEScopy InChI
Affinity DataKi:  490nMAssay Description:Inhibition constant against glutathione S-transferase pi using GSH (0.1-3mM), 1 mM 1-chloro-2,4-dinitrobenzeneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22R3R6RPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50173727(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(carboxy-...)copy SMILEScopy InChI
Affinity DataKi:  660nMAssay Description:Inhibition constant against glutathione S-transferase pi using GSH (0.1-3mM), 1 mM 1-chloro-2,4-dinitrobenzeneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22R3R6RPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)copy SMILEScopy InChI
Affinity DataKi:  840nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043764(2-Amino-4-{1-[(carboxy-phenyl-methyl)-carbamoyl]-2...)copy SMILEScopy InChI
Affinity DataKi:  850nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50173728(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(2-hydrox...)copy SMILEScopy InChI
Affinity DataKi:  1.11E+3nMAssay Description:Inhibition constant against glutathione S-transferase pi using GSH (0.1-3mM), 1 mM 1-chloro-2,4-dinitrobenzeneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22R3R6RPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50054194(CHEMBL3310886)copy SMILEScopy InChI
Affinity DataKi:  1.47E+3nMAssay Description:Competitive inhibition of human GSTA1 activity by double reciprocal Lineweaver-Burk graphMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P625BPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50295554(C6H5-SO2-Glu-Gln-Ser-Leu-Gly-Asn-Gln-Trp-Ala-Arg-G...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of human GSTA1-1 expressed in Escherichia coli BL21 (DE3) by 1-chloro-2,4-dinitrobenzene competitive assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182J4PubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50295556(C6H5-SO2-Glu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-G...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of human GSTA1-1 expressed in Escherichia coli BL21 (DE3) by 1-chloro-2,4-dinitrobenzene competitive assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182J4PubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50295555(C6H5-SO2-Glu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-G...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of human GSTA1-1 expressed in Escherichia coli BL21 (DE3) by 1-chloro-2,4-dinitrobenzene competitive assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182J4PubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50054205(CHEMBL3310889)copy SMILEScopy InChI
Affinity DataKi:  1.75E+3nMAssay Description:Competitive inhibition of human GSTA1 activity by double reciprocal Lineweaver-Burk graphMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P625BPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50038325(CHEMBL1234570)copy SMILEScopy InChI
Affinity DataKi:  1.85E+3nMAssay Description:Time dependent inhibition of GSTP1-1 (unknown origin) assessed as inhibition constant using reduced GSH and CDNB as substrate by spectrophotometric m...More data for this Ligand-Target Pair
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50043764(2-Amino-4-{1-[(carboxy-phenyl-methyl)-carbamoyl]-2...)copy SMILEScopy InChI
Affinity DataKi:  5.80E+3nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50148144(5-[1-Bromo-meth-(E)-ylidene]-3-((E)-styryl)-dihydr...)copy SMILEScopy InChI
Affinity DataKi:  6.10E+3nMAssay Description:Inhibitory activity of the compound for human Glutathione S-transferase P was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29C6WWWPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50295555(C6H5-SO2-Glu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-G...)copy SMILEScopy InChI
Affinity DataKi:  8.10E+3nMAssay Description:Inhibition of human GSTA1-1 expressed in Escherichia coli BL21 (DE3) by glutathione competitive assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182J4PubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50295556(C6H5-SO2-Glu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-G...)copy SMILEScopy InChI
Affinity DataKi:  8.10E+3nMAssay Description:Inhibition of human GSTA1-1 expressed in Escherichia coli BL21 (DE3) by glutathione competitive assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182J4PubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50295554(C6H5-SO2-Glu-Gln-Ser-Leu-Gly-Asn-Gln-Trp-Ala-Arg-G...)copy SMILEScopy InChI
Affinity DataKi:  8.10E+3nMAssay Description:Inhibition of human GSTA1-1 expressed in Escherichia coli BL21 (DE3) by glutathione competitive assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S182J4PubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50043760(2-Amino-4-[1-[(carboxy-phenyl-methyl)-carbamoyl]-2...)copy SMILEScopy InChI
Affinity DataKi:  1.47E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50043762(2-Amino-4-{2-benzylsulfanyl-1-[(carboxy-phenyl-met...)copy SMILEScopy InChI
Affinity DataKi:  2.43E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetMicrosomal glutathione S-transferase 1(Homo sapiens (Human))
Ondokuz Mayis University

LigandPNGBDBM50422689(640/359 | CEFUROXIME)copy SMILEScopy InChI
Affinity DataKi:  3.24E+4nM IC50: 5.64E+4nMpH: 6.5Assay Description:Enzymatic activity was determined spectrophotometrically by measuring the conjugation of CDNB with GSH. The 1 ml assay mixture contained 0.5 mM CDNB,...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21J98P4PubMed
TargetMicrosomal glutathione S-transferase 1(Homo sapiens (Human))
Ondokuz Mayis University

LigandPNGBDBM50049707((6R,7R)-7-{2-(2-Amino-thiazol-4-yl)-2-[(Z)-methoxy...)copy SMILEScopy InChI
Affinity DataKi:  3.54E+4nM IC50: 6.18E+4nMpH: 6.5Assay Description:Enzymatic activity was determined spectrophotometrically by measuring the conjugation of CDNB with GSH. The 1 ml assay mixture contained 0.5 mM CDNB,...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21J98P4PubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043763(2-Amino-4-[1-(2-carboxy-ethylcarbamoyl)-2-(4-methy...)copy SMILEScopy InChI
Affinity DataKi:  4.00E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50043763(2-Amino-4-[1-(2-carboxy-ethylcarbamoyl)-2-(4-methy...)copy SMILEScopy InChI
Affinity DataKi:  4.30E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50043761(2-Amino-4-[1-(2-carboxy-ethylcarbamoyl)-2-hexylsul...)copy SMILEScopy InChI
Affinity DataKi:  4.30E+4nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50395590(CHEMBL2165141)copy SMILEScopy InChI
Affinity DataKi:  7.10E+4nMAssay Description:Competitive inhibition of recombinant human GSTA1-1 expressed in Escherichia coli BL21 (DE3) using CDNB as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DN4654PubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50148143(5-[1-Bromo-meth-(E)-ylidene]-3-phenyl-dihydro-fura...)copy SMILEScopy InChI
Affinity DataKi:  1.24E+5nMAssay Description:Inhibitory activity of the compound for human glutathione S-transferase-pi isozyme was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29C6WWWPubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50395591(CHEMBL2165146)copy SMILEScopy InChI
Affinity DataKi:  1.35E+5nMAssay Description:Competitive inhibition of recombinant human GSTA1-1 expressed in Escherichia coli BL21 (DE3) using CDNB as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DN4654PubMed
TargetMicrosomal glutathione S-transferase 1(Homo sapiens (Human))
Ondokuz Mayis University

LigandPNGBDBM237182(Ceftizoxime)copy SMILEScopy InChI
Affinity DataKi:  1.65E+5nM IC50: 2.78E+5nMpH: 6.5Assay Description:Enzymatic activity was determined spectrophotometrically by measuring the conjugation of CDNB with GSH. The 1 ml assay mixture contained 0.5 mM CDNB,...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21J98P4PubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50173726(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(2-hydrox...)copy SMILEScopy InChI
Affinity DataKi:  1.87E+5nMAssay Description:Inhibition constant against glutathione S-transferase pi using GSH (0.1-3mM), 1 mM 1-chloro-2,4-dinitrobenzeneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22R3R6RPubMed
TargetMicrosomal glutathione S-transferase 1(Homo sapiens (Human))
Ondokuz Mayis University

LigandPNGBDBM50390999(CEFOPERAZONE)copy SMILEScopy InChI
Affinity DataKi:  2.67E+5nM IC50: 4.84E+5nMpH: 6.5Assay Description:Enzymatic activity was determined spectrophotometrically by measuring the conjugation of CDNB with GSH. The 1 ml assay mixture contained 0.5 mM CDNB,...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21J98P4PubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University of Athens

Curated by ChEMBL
LigandPNGBDBM50043759(2-Amino-4-[2-benzylsulfanyl-1-(2-carboxy-ethylcarb...)copy SMILEScopy InChI
Affinity DataKi:  3.60E+5nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione-S-transferase A1 enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043761(2-Amino-4-[1-(2-carboxy-ethylcarbamoyl)-2-hexylsul...)copy SMILEScopy InChI
Affinity DataKi:  5.50E+5nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043759(2-Amino-4-[2-benzylsulfanyl-1-(2-carboxy-ethylcarb...)copy SMILEScopy InChI
Affinity DataKi:  7.10E+5nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase PMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q21V5D1VPubMed