Found 30 hits of Enzyme Inhibition Constant Data Target/Host
(Institution) | Ligand | Target/Host
Links | Ligand
Links | Trg + Lig
Links | Ki
nM | ΔG°
kJ/mole | IC50
nM | Kd
nM | EC50/IC50
nM | koff
s-1 | kon
M-1s-1 | pH | Temp
°C |
|---|
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310309
(CHEMBL596879 | N-(3,4-dihydroxyphenylsulfonyl)-N-h...)Show SMILES CCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H23NO8S2/c1-2-3-4-5-10-19(28(24,25)13-6-8-15(20)17(22)11-13)29(26,27)14-7-9-16(21)18(23)12-14/h6-9,11-12,20-23H,2-5,10H2,1H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 284 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310311
(CHEMBL601265 | N-cyclohexyl-N-(3,4-dihydroxyphenyl...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(C1CCCCC1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H21NO8S2/c20-15-8-6-13(10-17(15)22)28(24,25)19(12-4-2-1-3-5-12)29(26,27)14-7-9-16(21)18(23)11-14/h6-12,20-23H,1-5H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 594 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310308
(CHEMBL597478 | N-(3,4-dihydroxyphenylsulfonyl)-3,4...)Show SMILES CCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C15H17NO8S2/c1-2-7-16(25(21,22)10-3-5-12(17)14(19)8-10)26(23,24)11-4-6-13(18)15(20)9-11/h3-6,8-9,17-20H,2,7H2,1H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 2.67E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310310
(CHEMBL596880 | N-benzyl-N-(3,4-dihydroxyphenylsulf...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(Cc1ccccc1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C19H17NO8S2/c21-16-8-6-14(10-18(16)23)29(25,26)20(12-13-4-2-1-3-5-13)30(27,28)15-7-9-17(22)19(24)11-15/h1-11,21-24H,12H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 4.82E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310301
(CHEMBL599742 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H24N2O8S2/c1-3-19(29(25,26)13-5-7-15(21)17(23)11-13)9-10-20(4-2)30(27,28)14-6-8-16(22)18(24)12-14/h5-8,11-12,21-24H,3-4,9-10H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 9.32E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310307
(CHEMBL596861 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1cc(F)c(O)c(F)c1)S(=O)(=O)c1cc(F)c(O)c(F)c1 Show InChI InChI=1S/C18H20F4N2O6S2/c1-3-23(31(27,28)11-7-13(19)17(25)14(20)8-11)5-6-24(4-2)32(29,30)12-9-15(21)18(26)16(22)10-12/h7-10,25-26H,3-6H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 1.28E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310306
(CHEMBL611972 | N,N'-(ethane-1,2-diyl)bis(N-ethylbe...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccccc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C18H24N2O4S2/c1-3-19(25(21,22)17-11-7-5-8-12-17)15-16-20(4-2)26(23,24)18-13-9-6-10-14-18/h5-14H,3-4,15-16H2,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310313
(CHEMBL596860 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-2...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1cc(O)ccc1O)S(=O)(=O)c1cc(O)ccc1O Show InChI InChI=1S/C18H24N2O8S2/c1-3-19(29(25,26)17-11-13(21)5-7-15(17)23)9-10-20(4-2)30(27,28)18-12-14(22)6-8-16(18)24/h5-8,11-12,21-24H,3-4,9-10H2,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310312
(CHEMBL597509 | N,N'-bis(3,4-dihydroxybenzenesulfon...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)N1CCN(CC1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C16H18N2O8S2/c19-13-3-1-11(9-15(13)21)27(23,24)17-5-7-18(8-6-17)28(25,26)12-2-4-14(20)16(22)10-12/h1-4,9-10,19-22H,5-8H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310312
(CHEMBL597509 | N,N'-bis(3,4-dihydroxybenzenesulfon...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)N1CCN(CC1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C16H18N2O8S2/c19-13-3-1-11(9-15(13)21)27(23,24)17-5-7-18(8-6-17)28(25,26)12-2-4-14(20)16(22)10-12/h1-4,9-10,19-22H,5-8H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310305
(CHEMBL596859 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-4...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccc(O)cc1)S(=O)(=O)c1ccc(O)cc1 Show InChI InChI=1S/C18H24N2O6S2/c1-3-19(27(23,24)17-9-5-15(21)6-10-17)13-14-20(4-2)28(25,26)18-11-7-16(22)8-12-18/h5-12,21-22H,3-4,13-14H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310299
(CHEMBL599342 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccc(OC)c(OC)c1)S(=O)(=O)c1ccc(OC)c(OC)c1 Show InChI InChI=1S/C22H32N2O8S2/c1-7-23(33(25,26)17-9-11-19(29-3)21(15-17)31-5)13-14-24(8-2)34(27,28)18-10-12-20(30-4)22(16-18)32-6/h9-12,15-16H,7-8,13-14H2,1-6H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310313
(CHEMBL596860 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-2...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1cc(O)ccc1O)S(=O)(=O)c1cc(O)ccc1O Show InChI InChI=1S/C18H24N2O8S2/c1-3-19(29(25,26)17-11-13(21)5-7-15(17)23)9-10-20(4-2)30(27,28)18-12-14(22)6-8-16(18)24/h5-8,11-12,21-24H,3-4,9-10H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310306
(CHEMBL611972 | N,N'-(ethane-1,2-diyl)bis(N-ethylbe...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccccc1)S(=O)(=O)c1ccccc1 Show InChI InChI=1S/C18H24N2O4S2/c1-3-19(25(21,22)17-11-7-5-8-12-17)15-16-20(4-2)26(23,24)18-13-9-6-10-14-18/h5-14H,3-4,15-16H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310305
(CHEMBL596859 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-4...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccc(O)cc1)S(=O)(=O)c1ccc(O)cc1 Show InChI InChI=1S/C18H24N2O6S2/c1-3-19(27(23,24)17-9-5-15(21)6-10-17)13-14-20(4-2)28(25,26)18-11-7-16(22)8-12-18/h5-12,21-22H,3-4,13-14H2,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310309
(CHEMBL596879 | N-(3,4-dihydroxyphenylsulfonyl)-N-h...)Show SMILES CCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H23NO8S2/c1-2-3-4-5-10-19(28(24,25)13-6-8-15(20)17(22)11-13)29(26,27)14-7-9-16(21)18(23)12-14/h6-9,11-12,20-23H,2-5,10H2,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310310
(CHEMBL596880 | N-benzyl-N-(3,4-dihydroxyphenylsulf...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(Cc1ccccc1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C19H17NO8S2/c21-16-8-6-14(10-18(16)23)29(25,26)20(12-13-4-2-1-3-5-13)30(27,28)15-7-9-17(22)19(24)11-15/h1-11,21-24H,12H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310311
(CHEMBL601265 | N-cyclohexyl-N-(3,4-dihydroxyphenyl...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(C1CCCCC1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H21NO8S2/c20-15-8-6-13(10-17(15)22)28(24,25)19(12-4-2-1-3-5-12)29(26,27)14-7-9-16(21)18(23)11-14/h6-12,20-23H,1-5H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310299
(CHEMBL599342 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccc(OC)c(OC)c1)S(=O)(=O)c1ccc(OC)c(OC)c1 Show InChI InChI=1S/C22H32N2O8S2/c1-7-23(33(25,26)17-9-11-19(29-3)21(15-17)31-5)13-14-24(8-2)34(27,28)18-10-12-20(30-4)22(16-18)32-6/h9-12,15-16H,7-8,13-14H2,1-6H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310304
(CHEMBL597510 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1cccc(O)c1)S(=O)(=O)c1cccc(O)c1 Show InChI InChI=1S/C18H24N2O6S2/c1-3-19(27(23,24)17-9-5-7-15(21)13-17)11-12-20(4-2)28(25,26)18-10-6-8-16(22)14-18/h5-10,13-14,21-22H,3-4,11-12H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 3.43E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310300
(CHEMBL606451 | N,N'-(ethane-1,2-diyl)bis(3,4-dihyd...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)NCCNS(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C14H16N2O8S2/c17-11-3-1-9(7-13(11)19)25(21,22)15-5-6-16-26(23,24)10-2-4-12(18)14(20)8-10/h1-4,7-8,15-20H,5-6H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 5.18E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310301
(CHEMBL599742 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H24N2O8S2/c1-3-19(29(25,26)13-5-7-15(21)17(23)11-13)9-10-20(4-2)30(27,28)14-6-8-16(22)18(24)12-14/h5-8,11-12,21-24H,3-4,9-10H2,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310304
(CHEMBL597510 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1cccc(O)c1)S(=O)(=O)c1cccc(O)c1 Show InChI InChI=1S/C18H24N2O6S2/c1-3-19(27(23,24)17-9-5-7-15(21)13-17)11-12-20(4-2)28(25,26)18-10-6-8-16(22)14-18/h5-10,13-14,21-22H,3-4,11-12H2,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310308
(CHEMBL597478 | N-(3,4-dihydroxyphenylsulfonyl)-3,4...)Show SMILES CCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C15H17NO8S2/c1-2-7-16(25(21,22)10-3-5-12(17)14(19)8-10)26(23,24)11-4-6-13(18)15(20)9-11/h3-6,8-9,17-20H,2,7H2,1H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >1.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310303
(CHEMBL599769 | N,N'-(hexane-1,6-diyl)bis(3,4-dihyd...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)NCCCCCCNS(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H24N2O8S2/c21-15-7-5-13(11-17(15)23)29(25,26)19-9-3-1-2-4-10-20-30(27,28)14-6-8-16(22)18(24)12-14/h5-8,11-12,19-24H,1-4,9-10H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.38E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310302
(CHEMBL611992 | N,N'-(butane-1,4-diyl)bis(3,4-dihyd...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)NCCCCNS(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C16H20N2O8S2/c19-13-5-3-11(9-15(13)21)27(23,24)17-7-1-2-8-18-28(25,26)12-4-6-14(20)16(22)10-12/h3-6,9-10,17-22H,1-2,7-8H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310307
(CHEMBL596861 | N,N'-(ethane-1,2-diyl)bis(N-ethyl-3...)Show SMILES CCN(CCN(CC)S(=O)(=O)c1cc(F)c(O)c(F)c1)S(=O)(=O)c1cc(F)c(O)c(F)c1 Show InChI InChI=1S/C18H20F4N2O6S2/c1-3-23(31(27,28)11-7-13(19)17(25)14(20)8-11)5-6-24(4-2)32(29,30)12-9-15(21)18(26)16(22)10-12/h7-10,25-26H,3-6H2,1-2H3 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | >3.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310300
(CHEMBL606451 | N,N'-(ethane-1,2-diyl)bis(3,4-dihyd...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)NCCNS(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C14H16N2O8S2/c17-11-3-1-9(7-13(11)19)25(21,22)15-5-6-16-26(23,24)10-2-4-12(18)14(20)8-10/h1-4,7-8,15-20H,5-6H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Antithrombin-III
(Homo sapiens (Human)) | BDBM50310303
(CHEMBL599769 | N,N'-(hexane-1,6-diyl)bis(3,4-dihyd...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)NCCCCCCNS(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C18H24N2O8S2/c21-15-7-5-13(11-17(15)23)29(25,26)19-9-3-1-2-4-10-20-30(27,28)14-6-8-16(22)18(24)12-14/h5-8,11-12,19-24H,1-4,9-10H2 | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of antithrombin-3 assessed as residual alpha-thrombin activity |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
Plasminogen activator inhibitor 1
(Homo sapiens (Human)) | BDBM50310302
(CHEMBL611992 | N,N'-(butane-1,4-diyl)bis(3,4-dihyd...)Show SMILES Oc1ccc(cc1O)S(=O)(=O)NCCCCNS(=O)(=O)c1ccc(O)c(O)c1 Show InChI InChI=1S/C16H20N2O8S2/c19-13-5-3-11(9-15(13)21)27(23,24)17-7-1-2-8-18-28(25,26)12-4-6-14(20)16(22)10-12/h3-6,9-10,17-22H,1-2,7-8H2 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | >3.00E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Eastern Michigan University
Curated by ChEMBL
| Assay Description
Inhibition of human recombinant PAI1 assessed as rate of AMC release after 30 mins |
Bioorg Med Chem Lett 20: 966-70 (2010)
Article DOI: 10.1016/j.bmcl.2009.12.051
BindingDB Entry DOI: 10.7270/Q24M94P3 |
More data for this
Ligand-Target Pair | |
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