Compile Data Set for Download or QSAR
Found 148 with Last Name = 'villoutreix' and Initial = 'bo'
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM32709((5-amino-3-pyridin-3-yl-1,2,4-triazol-1-yl)-(4-met...)copy SMILEScopy InChI
Affinity DataKi:  4.40E+3nMAssay Description:Inhibition of human kallikrein 5 measured after 15 mins at pH 8 by double-reciprocal plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetNeuropilin-1(Rattus norvegicus)
Universit£ Paris 13

Curated by ChEMBL
LigandPNGBDBM50317441(ATWLPPR | CHEMBL1095672)copy SMILEScopy InChI
Affinity DataKi:  5.20E+3nMAssay Description:Inhibition of biotinylated VEGF-A165 from rat recombinant NRP-1 Fc domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24Z2QPubMed
TargetNeuropilin-1(Rattus norvegicus)
Universit£ Paris 13

Curated by ChEMBL
LigandPNGBDBM50047413(CHEMBL1624864)copy SMILEScopy InChI
Affinity DataKi:  7.30E+3nMAssay Description:Inhibition of biotinylated VEGF-A165 from rat recombinant NRP-1 Fc domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24Z2QPubMed
TargetNeuropilin-1(Rattus norvegicus)
Universit£ Paris 13

Curated by ChEMBL
LigandPNGBDBM50047414(CHEMBL3311013)copy SMILEScopy InChI
Affinity DataKi:  9.40E+3nMAssay Description:Inhibition of biotinylated VEGF-A165 from rat recombinant NRP-1 Fc domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24Z2QPubMed
TargetNeuropilin-1(Rattus norvegicus)
Universit£ Paris 13

Curated by ChEMBL
LigandPNGBDBM50047415(CHEMBL1621063)copy SMILEScopy InChI
Affinity DataKi:  1.07E+4nMAssay Description:Inhibition of biotinylated VEGF-A165 from rat recombinant NRP-1 Fc domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24Z2QPubMed
TargetNeuropilin-1(Rattus norvegicus)
Universit£ Paris 13

Curated by ChEMBL
LigandPNGBDBM50047412(CHEMBL3311014)copy SMILEScopy InChI
Affinity DataKi:  1.13E+4nMAssay Description:Inhibition of biotinylated VEGF-A165 from rat recombinant NRP-1 Fc domainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C24Z2QPubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444601(CHEMBL3099881)copy SMILEScopy InChI
Affinity DataKi:  1.50E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444601(CHEMBL3099881)copy SMILEScopy InChI
Affinity DataKi:  4.40E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444600(CHEMBL1462676)copy SMILEScopy InChI
Affinity DataKi:  5.00E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444598(CHEMBL3099878)copy SMILEScopy InChI
Affinity DataKi:  5.50E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444604(CHEMBL3099870)copy SMILEScopy InChI
Affinity DataKi:  7.00E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444602(CHEMBL3099874)copy SMILEScopy InChI
Affinity DataKi:  7.20E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444603(CHEMBL3099871)copy SMILEScopy InChI
Affinity DataKi:  7.50E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444597(CHEMBL3099882)copy SMILEScopy InChI
Affinity DataKi:  8.30E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM50444597(CHEMBL3099882)copy SMILEScopy InChI
Affinity DataKi:  9.50E+4nMAssay Description:Competitive inhibition of human kallikrein5 using Boc-Val-Pro-Arg-AMC as substrate after 15 to 60 mins by Lineweaver-Burk/Eadie-Hofstee plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444599(CHEMBL3099875)copy SMILEScopy InChI
Affinity DataKi:  9.50E+4nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-inhibitor complex after 15 to 60 mins by Lin...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM50444602(CHEMBL3099874)copy SMILEScopy InChI
Affinity DataKi:  1.00E+5nMAssay Description:Competitive inhibition of human kallikrein5 using Boc-Val-Pro-Arg-AMC as substrate after 15 to 60 mins by Lineweaver-Burk/Eadie-Hofstee plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM50444603(CHEMBL3099871)copy SMILEScopy InChI
Affinity DataKi:  1.07E+5nMAssay Description:Competitive inhibition of human kallikrein5 using Boc-Val-Pro-Arg-AMC as substrate after 15 to 60 mins by Lineweaver-Burk/Eadie-Hofstee plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM50444604(CHEMBL3099870)copy SMILEScopy InChI
Affinity DataKi:  1.12E+5nMAssay Description:Competitive inhibition of human kallikrein5 using Boc-Val-Pro-Arg-AMC as substrate after 15 to 60 mins by Lineweaver-Burk/Eadie-Hofstee plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM50444598(CHEMBL3099878)copy SMILEScopy InChI
Affinity DataKi:  1.21E+5nMAssay Description:Competitive inhibition of human kallikrein5 using Boc-Val-Pro-Arg-AMC as substrate after 15 to 60 mins by Lineweaver-Burk/Eadie-Hofstee plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444604(CHEMBL3099870)copy SMILEScopy InChI
Affinity DataKi:  1.29E+5nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444598(CHEMBL3099878)copy SMILEScopy InChI
Affinity DataKi:  1.31E+5nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444599(CHEMBL3099875)copy SMILEScopy InChI
Affinity DataKi:  1.40E+5nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444603(CHEMBL3099871)copy SMILEScopy InChI
Affinity DataKi:  1.52E+5nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444602(CHEMBL3099874)copy SMILEScopy InChI
Affinity DataKi:  1.64E+5nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444600(CHEMBL1462676)copy SMILEScopy InChI
Affinity DataKi:  1.66E+5nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM50444597(CHEMBL3099882)copy SMILEScopy InChI
Affinity DataKi:  1.66E+5nMAssay Description:Mixed-type inhibition of human kallikrein7 using Suc-Leu-Leu-Val-Tyr-AMC as substrate assessed as enzyme-substrate-inhibitor complex after 15 to 60 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21837Z8PubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM32709((5-amino-3-pyridin-3-yl-1,2,4-triazol-1-yl)-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human kallikrein 7 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM51911((4-isopropoxybenzyl)-[3-(2-methoxyphenyl)-3-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of human kallikrein 5 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM33882((5-amino-3-pyridin-3-yl-1,2,4-triazol-1-yl)-(4-chl...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human kallikrein 7 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM33437((5-amino-3-phenyl-1,2,4-triazol-1-yl)-(3,4-dimetho...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:Inhibition of human kallikrein 7 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM32709((5-amino-3-pyridin-3-yl-1,2,4-triazol-1-yl)-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of human kallikrein 5 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM51911((4-isopropoxybenzyl)-[3-(2-methoxyphenyl)-3-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 420nMAssay Description:Inhibition of human matriptase measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM32709((5-amino-3-pyridin-3-yl-1,2,4-triazol-1-yl)-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 570nMAssay Description:Inhibition of human matriptase measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM33453((3-Amino-[1,2,4]triazol-4-yl)-(4-methoxy-phenyl)-m...)copy SMILEScopy InChI
Affinity DataIC50: 610nMAssay Description:Inhibition of human kallikrein 7 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-7(Homo sapiens (Human))
Universit£ Pierre et Marie Curie

Curated by ChEMBL
LigandPNGBDBM51911((4-isopropoxybenzyl)-[3-(2-methoxyphenyl)-3-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of human kallikrein 7 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-14(Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM51911((4-isopropoxybenzyl)-[3-(2-methoxyphenyl)-3-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 970nMAssay Description:Inhibition of human kallikrein 14 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM33453((3-Amino-[1,2,4]triazol-4-yl)-(4-methoxy-phenyl)-m...)copy SMILEScopy InChI
Affinity DataIC50: 990nMAssay Description:Inhibition of human kallikrein 5 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM33882((5-amino-3-pyridin-3-yl-1,2,4-triazol-1-yl)-(4-chl...)copy SMILEScopy InChI
Affinity DataIC50: 1.14E+3nMAssay Description:Inhibition of human kallikrein 5 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-14(Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM32709((5-amino-3-pyridin-3-yl-1,2,4-triazol-1-yl)-(4-met...)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+3nMAssay Description:Inhibition of human kallikrein 14 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetKallikrein-5 [D153N](Homo sapiens (Human))
Universit£ Pierre et Marie Curie-Sorbonne Universit£s (UPMC)

Curated by ChEMBL
LigandPNGBDBM33437((5-amino-3-phenyl-1,2,4-triazol-1-yl)-(3,4-dimetho...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human kallikrein 5 measured after 15 mins at pH 8 by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23B61JVPubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Universit£ Paris Descartes

Curated by ChEMBL
LigandPNGBDBM50402647(CHEMBL2206732)copy SMILEScopy InChI
Affinity DataIC50: 1.38E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67J38PubMed
TargetCoagulation factor V(Homo sapiens (Human))
Maastricht University

Curated by ChEMBL
LigandPNGBDBM50376425(CHEMBL1162108)copy SMILEScopy InChI
Affinity DataIC50: 1.81E+3nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190MGPubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Universit£ Paris Descartes

Curated by ChEMBL
LigandPNGBDBM24778(2-methyl-1,4-dihydronaphthalene-1,4-dione | 2-meth...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67J38PubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Universit£ Paris Descartes

Curated by ChEMBL
LigandPNGBDBM50402654(CHEMBL2207337)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67J38PubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Universit£ Paris Descartes

Curated by ChEMBL
LigandPNGBDBM50402665(CHEMBL2206740)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67J38PubMed
TargetCoagulation factor V(Homo sapiens (Human))
Maastricht University

Curated by ChEMBL
LigandPNGBDBM50376418(CHEMBL259312)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F190MGPubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Universit£ Paris Descartes

Curated by ChEMBL
LigandPNGBDBM50402650(CHEMBL2206756)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67J38PubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Universit£ Paris Descartes

Curated by ChEMBL
LigandPNGBDBM50402653(CHEMBL2206734)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67J38PubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
Universit£ Paris Descartes

Curated by ChEMBL
LigandPNGBDBM50402664(CHEMBL2206741)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of MBP-fused recombinant wild type CDC25B3 using fluorescein 3,6 diphosphate as substrate measured for 30 mins in presence of 1 mM dithiot...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J67J38PubMed
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