Compile Data Set for Download or QSAR
maximum 50k data
Found 1705 Enz. Inhib. hit(s) with Target = 'Glutathione S-transferase'
TargetGlutathione S-transferase theta-1(Rattus norvegicus)
Research Triangle Institute

Curated by ChEMBL
LigandPNGBDBM50368152(CHEMBL318812)
Affinity DataKi:  0.680nMAssay Description:The compound was tested for binding activity against muscarinic acetylcholine receptor M3, using [3H]-QNB as the radioligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM50155773(CHEMBL3781751 | US9469597, 5)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254553(US9469597, 12 | US9670136, 12 4-(((trans)-2-(6-(3-...)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254603(US10214477, Example 5 | US9469597, 4 | US9670136, ...)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254556(US10214477, Example 15 | US9469597, 15 | US9670136...)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM50142189(CHEMBL3759239 | US10329256, Example 5 | US9487512,...)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
LigandPNGBDBM256457(US9487512, 1)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
LigandPNGBDBM256459(US10329256, Example 3 | US9487512, 3 | US9944601, ...)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254546(US10214477, Example 3 | US9469597, 1 | US9670136, ...)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
LigandPNGBDBM256460(US9487512, 4)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM256461(US10329256, Example 6 | US9487512, 6 | US9944601, ...)
Affinity DataKi:  50nM ΔG°:  -43.3kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043760(2-Amino-4-[1-[(carboxy-phenyl-methyl)-carbamoyl]-2...)
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 ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50562986(CHEMBL4757438)
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 ArticlePubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University Of Athens

Curated by ChEMBL
LigandPNGBDBM50054198(CHEMBL3310888)
Affinity DataKi:  360nMAssay Description:Competitive inhibition of human GSTA1 activity by double reciprocal Lineweaver-Burk graphMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University Of Athens

Curated by ChEMBL
LigandPNGBDBM50054196(CHEMBL3310887)
Affinity DataKi:  380nMAssay Description:Competitive inhibition of human GSTA1 activity by double reciprocal Lineweaver-Burk graphMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043762(2-Amino-4-{2-benzylsulfanyl-1-[(carboxy-phenyl-met...)
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 ArticlePubMed
TargetGlutathione S-transferase omega-1(Homo sapiens (Human))
Monash University

Curated by ChEMBL
LigandPNGBDBM50458516(CHEMBL4210652)
Affinity DataKi:  440nMAssay Description:Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione ...More data for this Ligand-Target Pair
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50173725(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(2-hydrox...)
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 ArticlePubMed
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254555(US10214477, Example 14 | US9469597, 14 | US9670136...)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254554(US10214477, Example 13 | US9469597, 13 | US9670136...)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254552(US9469597, 11 | US9670136, 11 4-(((trans)-2-(6-(3-...)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254549(US10214477, Example 8 | US9469597, 8 | US9670136, ...)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254602(US9469597, 3)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetGlutathione S-transferase P/Lysine-specific histone demethylase 1A [158-852](Homo sapiens (Human))
Oryzon Genomics

US Patent
LigandPNGBDBM254601(US9469597, 2)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
LigandPNGBDBM256464(US10329256, Example 9 | US9487512, 9 | US9944601, ...)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM256462(US10329256, Example 7 | US9487512, 7 | US9944601, ...)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM256458(US10329256, Example 2 | US9487512, 2 | US9944601, ...)
Affinity DataKi:  550nM ΔG°:  -37.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetGlutathione S-transferase omega-1(Homo sapiens (Human))
Monash University

Curated by ChEMBL
LigandPNGBDBM50527166(CHEMBL4589666)
Affinity DataKi:  610nMAssay Description:Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50173727(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(carboxy-...)
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 ArticlePubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University Of Athens

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)
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 ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043764(2-Amino-4-{1-[(carboxy-phenyl-methyl)-carbamoyl]-2...)
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 ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50173728(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(2-hydrox...)
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 ArticlePubMed
TargetGlutathione S-transferase omega-1(Homo sapiens (Human))
Monash University

Curated by ChEMBL
LigandPNGBDBM50527182(CHEMBL4458115)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University Of Athens

Curated by ChEMBL
LigandPNGBDBM50054194(CHEMBL3310886)
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 ArticlePubMed
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...)
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 ArticlePubMed
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...)
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 ArticlePubMed
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...)
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 ArticlePubMed
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University Of Athens

Curated by ChEMBL
LigandPNGBDBM50054205(CHEMBL3310889)
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 ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50038325(CHEMBL1234570)
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 Mu 1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043758(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-hexylsulf...)
Affinity DataKi:  2.00E+3nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase Mu 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase Mu 1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50043763(2-Amino-4-[1-(2-carboxy-ethylcarbamoyl)-2-(4-methy...)
Affinity DataKi:  2.10E+3nMAssay Description:Inhibitory activity of the compound was measured on recombinant human Glutathione S-transferase Mu 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase omega-1(Homo sapiens (Human))
Monash University

Curated by ChEMBL
LigandPNGBDBM50527163(CHEMBL4445050)
Affinity DataKi:  2.50E+3nMAssay Description:Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase Mu 1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50361800(CHEMBL1938641)
Affinity DataKi:  3.20E+3nMAssay Description:Competitive inhibition of human GSTM1 using GSH as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase Mu 1(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50361800(CHEMBL1938641)
Affinity DataKi:  4.70E+3nMAssay Description:Noncompetitive inhibition of human GSTM1 using CDNB as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase omega-1(Homo sapiens (Human))
Monash University

Curated by ChEMBL
LigandPNGBDBM50527184(CHEMBL4454026)
Affinity DataKi:  4.80E+3nMAssay Description:Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetGlutathione S-transferase omega-1(Homo sapiens (Human))
Monash University

Curated by ChEMBL
LigandPNGBDBM50527185(CHEMBL4580168)
Affinity DataKi:  5.00E+3nMAssay Description:Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
LigandPNGBDBM256463(US10329256, Example 8 | US9487512, 8 | US9944601, ...)
Affinity DataKi:  5.50E+3nM ΔG°:  -31.2kJ/molepH: 7.4 T: 2°CAssay Description:The compounds of the invention can be tested for their ability to inhibit LSD1. The ability of the compounds of the invention to inhibit LSD1 can be ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetGlutathione S-transferase A1(Homo sapiens (Human))
Agricultural University Of Athens

Curated by ChEMBL
LigandPNGBDBM50043764(2-Amino-4-{1-[(carboxy-phenyl-methyl)-carbamoyl]-2...)
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 ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
Terrapin Technologies

Curated by ChEMBL
LigandPNGBDBM50148144(5-[1-Bromo-meth-(E)-ylidene]-3-((E)-styryl)-dihydr...)
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 ArticlePubMed
TargetGlutathione S-transferase omega-1(Homo sapiens (Human))
Monash University

Curated by ChEMBL
LigandPNGBDBM50527167(CHEMBL4445668)
Affinity DataKi:  6.70E+3nMAssay Description:Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione ...More data for this Ligand-Target Pair
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