Compile Data Set for Download or QSAR
maximum 50k data
Found 60 Enz. Inhib. hit(s) with all data for entry = 50011309
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50162774(ABT-199 | US11420968, Example ABT-199 | Venetoclax)
Affinity DataKi: <0.0100nMAssay Description:Inhibition of BCL2 (unknown origin) by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCaspase-3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546262(CHEMBL4751195)
Affinity DataKi:  0.0800nMAssay Description:Inhibition of caspase-3 (unknown origin) using Ac-DEVD-AMCA as substrate incubated for 5 mins by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50270877((R)-4-(4-((2-(4-chlorophenyl)-5,5-dimethylcyclohex...)
Affinity DataKi: <0.5nMAssay Description:Inhibition of BCL2 (unknown origin) by TR-FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM13954(3-({5-[(2S)-3-{4-[(2-carboxyphenyl)amidoformic aci...)
Affinity DataKi:  22nMAssay Description:Inhibition of PTP1B (unknown origin) using pNPP as substrate measured every 30 secs for 15 mins by Michaelis-Menten plot analysisMore data for this Ligand-Target Pair
TargetCaspase-3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546260(CHEMBL4782926)
Affinity DataKi:  25nMAssay Description:Inhibition of caspase-3 (unknown origin) using Ac-DEVD-AMCA as substrate incubated for 5 mins by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50462575(CHEMBL4238121)
Affinity DataKi:  29nMAssay Description:Inhibition of human factor 10a using Boc-Leu-Gly-Arg-AMC as fluorogenic substrate measured after 10 mins by spectrofluorimetryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetCaspase-3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM220(5-{[(4-{[(2S)-1-carboxy-3-oxopropan-2-yl]carbamoyl...)
Affinity DataKi:  200nMAssay Description:Inhibition of recombinant human caspase 3 using Ac-Asp-Glu-Val-Asp-AFC as substrate preincubated for 30 mins followed by substrate addition and measu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546250(CHEMBL4754689)
Affinity DataKi:  1.90E+3nMAssay Description:Displacement of biotin-labelled geldanamycin from human HSP90 (D9 to E236 residues) incubated for 3 hrs by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546251(CHEMBL4783360)
Affinity DataKi:  4.00E+3nMAssay Description:Inhibition of human HSP90 (D9 to E236 residues) by fluorescence spectroscopyMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM13990(5-{2-fluoro-5-[(1E)-3-[3-hydroxy-2-(methoxycarbony...)
Affinity DataKi:  7.00E+3nMAssay Description:Inhibition of PTP1B (unknown origin) using pNPP as substrate measured every 30 secs for 15 mins by Michaelis-Menten plot analysisMore data for this Ligand-Target Pair
TargetCaspase-3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546261(CHEMBL234378)
Affinity DataKi:  1.20E+5nMAssay Description:Inhibition of caspase-3 (unknown origin) using Ac-DEVD-AMCA as substrate incubated for 5 mins by Dixon plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50232690(4-Aminomethyl-Benzamidine | CHEMBL187301)
Affinity DataKi:  6.80E+5nMAssay Description:Inhibition of human factor 10a using Boc-Leu-Gly-Arg-AMC as fluorogenic substrate measured after 10 mins by spectrofluorimetryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50514418(CHEMBL4572188)
Affinity DataKi:  5.50E+6nMAssay Description:Inhibition of human factor 10a using Boc-Leu-Gly-Arg-AMC as fluorogenic substrate measured after 10 mins by spectrofluorimetryMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
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Curated by ChEMBL
LigandPNGBDBM9047(Bis-THA inhibitor 5 | CHEMBL73800 | Hexylene-Linke...)
Affinity DataIC50:  0.400nMAssay Description:Inhibition of rat brain Acetylcholinesterase using acetylthiocholine as substrate in presence of BChE inhibitor ethopropazineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50520331(CHEMBL4445137)
Affinity DataIC50: <1nMAssay Description:Inhibition of human NMT1 by fluorescence methodMore data for this Ligand-Target Pair
TargetStromelysin-1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50149219(3-(3'-Cyanomethyl-biphenyl-4-yloxy)-N-hydroxy-prop...)
Affinity DataIC50:  15nMAssay Description:Inhibition of MMP3 (unknown origin) using Ac-Pro-Leu-Gly-[2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt as substrate incubated for 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChitinase B(Serratia marcescens)
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Curated by ChEMBL
LigandPNGBDBM50462584(CHEMBL4245260)
Affinity DataIC50:  22nMAssay Description:Inhibition of Serratia marcescens chitinase BMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50504620(GW280670X)
Affinity DataIC50:  30nMAssay Description:Inhibition of CDK2/Cyclin A (unknown origin) using histone H1 as substrate by scintillation counting methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetEndothiapepsin(Cryphonectria parasitica)
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Curated by ChEMBL
LigandPNGBDBM50546276(CHEMBL4743297)
Affinity DataIC50:  54nMAssay Description:Inhibition of Endothia parasitica endothiapepsin using Abz-Thr-Ile-Nle-p-nitro-Phe-Gln-Arg-NH2 as substrate by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546256(CHEMBL4793660)
Affinity DataIC50:  64nMAssay Description:Inhibition of c-Src (unknown origin) using biotin-KVEKIGEGTYGVVYK as substrate by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50181873(CHEMBL383229 | N-[4-(4,4-dimethylpiperidin-1-yl)be...)
Affinity DataIC50:  79nMAssay Description:Inhibition of FITC-labeled Bak BH3 peptide binding to His6-tagged GST-fused Bcl-xL (unknown origin) expressed in Escherichia coli BL21 preincubated f...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase B(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546259(CHEMBL4092230)
Affinity DataIC50:  80nMAssay Description:Inhibition of C-terminal His6-tagged CypB (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546259(CHEMBL4092230)
Affinity DataIC50:  100nMAssay Description:Inhibition of C-terminal His6-tagged CypA (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546269(CHEMBL4761368)
Affinity DataIC50:  510nMAssay Description:Inhibition of HDAC8 (unknown origin) using acetylated lysine as substrate incubated for 20 mins by Lineweaver-Burk double-reciprocal plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetChitinase B(Serratia marcescens)
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Curated by ChEMBL
LigandPNGBDBM50546270(CHEMBL4754642)
Affinity DataIC50:  580nMAssay Description:Inhibition of Serratia marcescens chitinase BMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
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Curated by ChEMBL
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)
Affinity DataIC50:  600nMAssay Description:Inhibition of rat brain Acetylcholinesterase using acetylthiocholine as substrate in presence of BChE inhibitor ethopropazineMore data for this Ligand-Target Pair
TargetHistone deacetylase 8(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546266(CHEMBL4779796)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of HDAC8 (unknown origin) using acetylated lysine as substrate incubated for 20 mins by Lineweaver-Burk double-reciprocal plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546254(CHEMBL1236930)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of N-terminal HSP90A (unknown origin) incubated for 60 mins by TAMRA fluorescence-based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetHistone deacetylase 8(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546268(CHEMBL4748996)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of HDAC8 (unknown origin) using acetylated lysine as substrate incubated for 20 mins by Lineweaver-Burk double-reciprocal plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase B(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM139995(US8901295, F428)
Affinity DataIC50:  6.10E+3nMAssay Description:Inhibition of C-terminal His6-tagged CypB (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails ArticlePubMed
TargetEndothiapepsin(Cryphonectria parasitica)
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Curated by ChEMBL
LigandPNGBDBM50546275(CHEMBL4797373)
Affinity DataIC50:  1.28E+4nMAssay Description:Inhibition of Endothia parasitica endothiapepsin using Abz-Thr-Ile-Nle-p-nitro-Phe-Gln-Arg-NH2 as substrate by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM139995(US8901295, F428)
Affinity DataIC50:  1.31E+4nMAssay Description:Inhibition of C-terminal His6-tagged CypA (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50520334(CHEMBL4591961)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibition of human NMT1 by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546255(CHEMBL4780637)
Affinity DataIC50:  4.00E+4nMAssay Description:Inhibition of c-Src (unknown origin) using biotin-KVEKIGEGTYGVVYK as substrate by ELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50149225(3,4-Dihydroxy-benzaldehyde O-methyl-oxime | CHEMBL...)
Affinity DataIC50:  4.10E+4nMAssay Description:Inhibition of c-Src (unknown origin) using biotin-KVEKIGEGTYGVVYK as substrate by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEndothiapepsin(Cryphonectria parasitica)
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Curated by ChEMBL
LigandPNGBDBM50546277(CHEMBL4747458)
Affinity DataIC50:  4.30E+4nMAssay Description:Inhibition of Endothia parasitica endothiapepsin using Abz-Thr-Ile-Nle-p-nitro-Phe-Gln-Arg-NH2 as substrate by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycylpeptide N-tetradecanoyltransferase 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546274(CHEMBL1740332)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human NMT1 by fluorescence methodMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails ArticlePubMed
TargetChitinase B(Serratia marcescens)
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Curated by ChEMBL
LigandPNGBDBM50546271(CHEMBL4740592)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of Serratia marcescens chitinase BMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546272(CHEMBL4747123)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of FITC-labeled Bak BH3 peptide binding to His6-tagged GST-fused Bcl-xL (unknown origin) expressed in Escherichia coli BL21 preincubated f...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546273(CHEMBL4749218)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of FITC-labeled Bak BH3 peptide binding to His6-tagged GST-fused Bcl-xL (unknown origin) expressed in Escherichia coli BL21 preincubated f...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM10858(4-hydrazinylbenzene-1-sulfonamide | CHEMBL7204 | a...)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of CDK2/Cyclin A (unknown origin) using histone H1 as substrate by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546267(CHEMBL3236141)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of HDAC8 (unknown origin) using acetylated lysine as substrate incubated for 20 mins by Lineweaver-Burk double-reciprocal plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM22813(5-chloro-2,3-dihydro-1H-indole-2,3-dione | Isatin-...)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of CDK2/Cyclin A (unknown origin) using histone H1 as substrate by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546253(CHEMBL1230058)
Affinity DataIC50:  1.00E+6nMAssay Description:Inhibition of HSP90 (unknown origin) by confocal fluorescence-based biochemical assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetHeat shock protein HSP 90-alpha/90-beta(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM92422(CHEMBL407391 | PU09)
Affinity DataIC50:  1.50E+6nMAssay Description:Inhibition of HSP90 (unknown origin) by confocal fluorescence-based biochemical assayMore data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546257(CHEMBL3408644)
Affinity DataIC50: >5.00E+6nMAssay Description:Inhibition of C-terminal His6-tagged CypA (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546258(CHEMBL4745604)
Affinity DataIC50: >5.00E+6nMAssay Description:Inhibition of C-terminal His6-tagged CypA (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase B(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50546258(CHEMBL4745604)
Affinity DataIC50: >5.00E+6nMAssay Description:Inhibition of C-terminal His6-tagged CypB (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeptidyl-prolyl cis-trans isomerase B(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50546257(CHEMBL3408644)
Affinity DataIC50: >5.00E+6nMAssay Description:Inhibition of C-terminal His6-tagged CypB (unknown origin) expressed in Escherichia coli C41(DE3) using Suc-Ala-Ala-Cis-Pro-Phe-pNA as substrate by s...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50133281(5-(4-Bromo-phenyl)-isoxazole-3-carboxylic acid | C...)
Affinity DataKd:  8.00E+5nMAssay Description:Binding affinity to N-terminal GST-fused human PTP1B (1 to 288 residues) expressed in Escherichia coli BL21(DE3) by HSQC NMR analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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