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Found 264 hits Enz. Inhib. hit(s) with Target = 'Plasminogen' AND taxid = 9913   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Plasminogen


(Bos taurus)
BDBM50113792
PNG
(CHEMBL81521 | S-4-{2-[2-(1-Carbamimidoyl-piperidin...)
Show SMILES CN([C@@H](CC(O)=O)C(=O)N1CCCC[C@H]1CCOC1CCN(CC1)C(N)=N)C1CCCCC1
Show InChI InChI=1S/C24H43N5O4/c1-27(18-7-3-2-4-8-18)21(17-22(30)31)23(32)29-13-6-5-9-19(29)12-16-33-20-10-14-28(15-11-20)24(25)26/h18-21H,2-17H2,1H3,(H3,25,26)(H,30,31)/t19-,21-/m0/s1
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Similars

PubMed
3.30n/an/an/an/an/an/an/an/a



Pfizer Global Research and Development

Curated by ChEMBL


Assay Description
Inhibitory effect on plasmin in bovine plasma


J Med Chem 45: 2432-53 (2002)


BindingDB Entry DOI: 10.7270/Q2S181VR
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264615
PNG
(US9718760, C182)
Show SMILES CCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C19H25NO8S2/c1-2-3-4-5-6-11-20(29(25,26)14-7-9-16(21)18(23)12-14)30(27,28)15-8-10-17(22)19(24)13-15/h7-10,12-13,21-24H,2-6,11H2,1H3
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n/an/a 33n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264650
PNG
(US9718760, C204)
Show SMILES Oc1ccc(cc1O)C(=O)OCC(CNS(=O)(=O)c1cccc(c1)C(F)(F)F)OC(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C24H20F3NO10S/c25-24(26,27)15-2-1-3-17(10-15)39(35,36)28-11-16(38-23(34)14-5-7-19(30)21(32)9-14)12-37-22(33)13-4-6-18(29)20(31)8-13/h1-10,16,28-32H,11-12H2
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n/an/a 35n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264630
PNG
(US9718760, C198)
Show SMILES Oc1ccc(CCNS(=O)(=O)c2ccc(O)c(O)c2)cc1O
Show InChI InChI=1S/C14H15NO6S/c16-11-3-1-9(7-13(11)18)5-6-15-22(20,21)10-2-4-12(17)14(19)8-10/h1-4,7-8,15-19H,5-6H2
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n/an/a 51n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264611
PNG
(US9718760, C188)
Show SMILES CCCCCCc1ccc(cc1)N(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C24H27NO8S2/c1-2-3-4-5-6-17-7-9-18(10-8-17)25(34(30,31)19-11-13-21(26)23(28)15-19)35(32,33)20-12-14-22(27)24(29)16-20/h7-16,26-29H,2-6H2,1H3
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n/an/a 120n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264602
PNG
(US9718760, C197)
Show SMILES Oc1ccc(CCN(S(=O)(=O)c2ccccc2)S(=O)(=O)c2ccc(O)c(O)c2)cc1O
Show InChI InChI=1S/C20H19NO8S2/c22-17-8-6-14(12-19(17)24)10-11-21(30(26,27)15-4-2-1-3-5-15)31(28,29)16-7-9-18(23)20(25)13-16/h1-9,12-13,22-25H,10-11H2
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n/an/a 173n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264616
PNG
(US9718760, C183)
Show SMILES CCCCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C21H29NO8S2/c1-2-3-4-5-6-7-8-13-22(31(27,28)16-9-11-18(23)20(25)14-16)32(29,30)17-10-12-19(24)21(26)15-17/h9-12,14-15,23-26H,2-8,13H2,1H3
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n/an/a 180n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264613
PNG
(US9718760, C157)
Show SMILES CCCCCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C22H31NO8S2/c1-2-3-4-5-6-7-8-9-14-23(32(28,29)17-10-12-19(24)21(26)15-17)33(30,31)18-11-13-20(25)22(27)16-18/h10-13,15-16,24-27H,2-9,14H2,1H3
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n/an/a 250n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264609
PNG
(US9718760, C163)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(c1cccc(c1)C(F)(F)F)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C19H14F3NO8S2/c20-19(21,22)11-2-1-3-12(8-11)23(32(28,29)13-4-6-15(24)17(26)9-13)33(30,31)14-5-7-16(25)18(27)10-14/h1-10,24-27H
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n/an/a 288n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264610
PNG
(US9718760, C165)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(c1ccc(cc1)-c1ccccc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C24H19NO8S2/c26-21-12-10-19(14-23(21)28)34(30,31)25(35(32,33)20-11-13-22(27)24(29)15-20)18-8-6-17(7-9-18)16-4-2-1-3-5-16/h1-15,26-29H
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n/an/a 350n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264645
PNG
(US9718760, C185)
Show SMILES CCCCCCCCCN(CCN(CCCCCCCCC)S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C32H52N2O8S2/c1-3-5-7-9-11-13-15-21-33(43(39,40)27-17-19-29(35)31(37)25-27)23-24-34(22-16-14-12-10-8-6-4-2)44(41,42)28-18-20-30(36)32(38)26-28/h17-20,25-26,35-38H,3-16,21-24H2,1-2H3
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n/an/a 420n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264646
PNG
(US9718760, C196)
Show SMILES CCCCCCCCCCN(CCN(C)S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C25H38N2O8S2/c1-3-4-5-6-7-8-9-10-15-27(37(34,35)21-12-14-23(29)25(31)19-21)17-16-26(2)36(32,33)20-11-13-22(28)24(30)18-20/h11-14,18-19,28-31H,3-10,15-17H2,1-2H3
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n/an/a 450n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264610
PNG
(US9718760, C165)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(c1ccc(cc1)-c1ccccc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C24H19NO8S2/c26-21-12-10-19(14-23(21)28)34(30,31)25(35(32,33)20-11-13-22(27)24(29)15-20)18-8-6-17(7-9-18)16-4-2-1-3-5-16/h1-15,26-29H
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n/an/a 510n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264644
PNG
(US9718760, C184)
Show SMILES CCCCCCCN(CCN(CCCCCCC)S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C28H44N2O8S2/c1-3-5-7-9-11-17-29(39(35,36)23-13-15-25(31)27(33)21-23)19-20-30(18-12-10-8-6-4-2)40(37,38)24-14-16-26(32)28(34)22-24/h13-16,21-22,31-34H,3-12,17-20H2,1-2H3
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n/an/a 590n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264609
PNG
(US9718760, C163)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(c1cccc(c1)C(F)(F)F)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C19H14F3NO8S2/c20-19(21,22)11-2-1-3-12(8-11)23(32(28,29)13-4-6-15(24)17(26)9-13)33(30,31)14-5-7-16(25)18(27)10-14/h1-10,24-27H
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n/an/a 611n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264643
PNG
(US9718760, C176)
Show SMILES CCCCCCCCN(CCN(CCCCCCCC)S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C30H48N2O8S2/c1-3-5-7-9-11-13-19-31(41(37,38)25-15-17-27(33)29(35)23-25)21-22-32(20-14-12-10-8-6-4-2)42(39,40)26-16-18-28(34)30(36)24-26/h15-18,23-24,33-36H,3-14,19-22H2,1-2H3
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n/an/a 620n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264607
PNG
(US9718760, C153)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(c1ccccc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C18H15NO8S2/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/h1-11,20-23H
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n/an/a 700n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264628
PNG
(US9718760, C187)
Show SMILES CCCCCCc1ccc(NS(=O)(=O)c2ccc(O)c(O)c2)cc1
Show InChI InChI=1S/C18H23NO4S/c1-2-3-4-5-6-14-7-9-15(10-8-14)19-24(22,23)16-11-12-17(20)18(21)13-16/h7-13,19-21H,2-6H2,1H3
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n/an/a 910n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264612
PNG
(US9718760, C195)
Show SMILES CCCCCCCCCCCCc1ccc(cc1)N(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C30H39NO8S2/c1-2-3-4-5-6-7-8-9-10-11-12-23-13-15-24(16-14-23)31(40(36,37)25-17-19-27(32)29(34)21-25)41(38,39)26-18-20-28(33)30(35)22-26/h13-22,32-35H,2-12H2,1H3
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n/an/a 920n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264613
PNG
(US9718760, C157)
Show SMILES CCCCCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C22H31NO8S2/c1-2-3-4-5-6-7-8-9-14-23(32(28,29)17-10-12-19(24)21(26)15-17)33(30,31)18-11-13-20(25)22(27)16-18/h10-13,15-16,24-27H,2-9,14H2,1H3
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n/an/a 980n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264607
PNG
(US9718760, C153)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(c1ccccc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C18H15NO8S2/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/h1-11,20-23H
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n/an/a 1.02E+3n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen


(Bos taurus)
BDBM50046896
PNG
(2-Acetylamino-4-methyl-pentanoic acid [1-(1-formyl...)
Show SMILES [#6]-[#6](-[#6])-[#6]-[#6@H](-[#7]-[#6](-[#6])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-c1ccccc1)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6]=O |r|
Show InChI InChI=1S/C23H36N6O4/c1-15(2)12-19(27-16(3)31)22(33)29-20(13-17-8-5-4-6-9-17)21(32)28-18(14-30)10-7-11-26-23(24)25/h4-6,8-9,14-15,18-20H,7,10-13H2,1-3H3,(H,27,31)(H,28,32)(H,29,33)(H4,24,25,26)/t18-,19-,20-/m0/s1
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n/an/a 1.10E+3n/an/an/an/an/an/a



University of Arkansas

Curated by ChEMBL


Assay Description
Inhibition of plasmin with Val-L-Leu-L-lysine-p-nitroanilide as substrate


J Med Chem 36: 1084-9 (1993)


BindingDB Entry DOI: 10.7270/Q24F1RCR
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264601
PNG
(US9718760, C191)
Show SMILES CCCCCCCCN(S(=O)(=O)c1ccc(CCCCC)cc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C25H37NO6S2/c1-3-5-7-8-9-11-19-26(34(31,32)23-17-18-24(27)25(28)20-23)33(29,30)22-15-13-21(14-16-22)12-10-6-4-2/h13-18,20,27-28H,3-12,19H2,1-2H3
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n/an/a 1.28E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264623
PNG
(US9718760, C180)
Show SMILES CCCCCCCCN(CCCCCC)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C20H35NO4S/c1-3-5-7-9-10-12-16-21(15-11-8-6-4-2)26(24,25)18-13-14-19(22)20(23)17-18/h13-14,17,22-23H,3-12,15-16H2,1-2H3
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n/an/a 1.34E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264614
PNG
(US9718760, C158)
Show SMILES CCCCCCCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C24H35NO8S2/c1-2-3-4-5-6-7-8-9-10-11-16-25(34(30,31)19-12-14-21(26)23(28)17-19)35(32,33)20-13-15-22(27)24(29)18-20/h12-15,17-18,26-29H,2-11,16H2,1H3
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n/an/a 1.44E+3n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen


(Bos taurus)
BDBM50046887
PNG
(2-(2-Acetylamino-3-phenyl-propionylamino)-4-methyl...)
Show SMILES [#6]-[#6](-[#6])-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccccc1)-[#7]-[#6](-[#6])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6]=O |r|
Show InChI InChI=1S/C23H36N6O4/c1-15(2)12-19(21(32)28-18(14-30)10-7-11-26-23(24)25)29-22(33)20(27-16(3)31)13-17-8-5-4-6-9-17/h4-6,8-9,14-15,18-20H,7,10-13H2,1-3H3,(H,27,31)(H,28,32)(H,29,33)(H4,24,25,26)/t18-,19-,20-/m0/s1
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University of Arkansas

Curated by ChEMBL


Assay Description
Inhibition of plasmin with Val-L-Leu-L-lysine-p-nitroanilide as substrate


J Med Chem 36: 1084-9 (1993)


BindingDB Entry DOI: 10.7270/Q24F1RCR
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264597
PNG
(US9718760, C152)
Show SMILES CCCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1cc(F)c(O)c(F)c1
Show InChI InChI=1S/C20H25F2NO7S2/c1-2-3-4-5-6-7-10-23(31(27,28)14-8-9-18(24)19(25)13-14)32(29,30)15-11-16(21)20(26)17(22)12-15/h8-9,11-13,24-26H,2-7,10H2,1H3
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n/an/a 1.57E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264618
PNG
(US9718760, C171)
Show SMILES CCCCCCN(CCCCCC)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C18H31NO4S/c1-3-5-7-9-13-19(14-10-8-6-4-2)24(22,23)16-11-12-17(20)18(21)15-16/h11-12,15,20-21H,3-10,13-14H2,1-2H3
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n/an/a 1.67E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264597
PNG
(US9718760, C152)
Show SMILES CCCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1cc(F)c(O)c(F)c1
Show InChI InChI=1S/C20H25F2NO7S2/c1-2-3-4-5-6-7-10-23(31(27,28)14-8-9-18(24)19(25)13-14)32(29,30)15-11-16(21)20(26)17(22)12-15/h8-9,11-13,24-26H,2-7,10H2,1H3
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n/an/a 1.71E+3n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264635
PNG
(US9718760, C271)
Show SMILES OC(=O)CCCCCNS(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C12H17NO6S/c14-10-6-5-9(8-11(10)15)20(18,19)13-7-3-1-2-4-12(16)17/h5-6,8,13-15H,1-4,7H2,(H,16,17)
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n/an/a 1.82E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264642
PNG
(US9718760, C168)
Show SMILES CCCCCCCCCCN(CCN(CCCCCCCCCC)S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C34H56N2O8S2/c1-3-5-7-9-11-13-15-17-23-35(45(41,42)29-19-21-31(37)33(39)27-29)25-26-36(24-18-16-14-12-10-8-6-4-2)46(43,44)30-20-22-32(38)34(40)28-30/h19-22,27-28,37-40H,3-18,23-26H2,1-2H3
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n/an/a 1.98E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264619
PNG
(US9718760, C172)
Show SMILES CCCCCCCCN(Cc1cc(Cl)c(O)c(Cl)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C21H27Cl2NO5S/c1-2-3-4-5-6-7-10-24(14-15-11-17(22)21(27)18(23)12-15)30(28,29)16-8-9-19(25)20(26)13-16/h8-9,11-13,25-27H,2-7,10,14H2,1H3
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n/an/a 1.98E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264648
PNG
(US9718760, C161)
Show SMILES CCCCCCCCNC(=O)c1cc(O)c(O)c(O)c1
Show InChI InChI=1S/C15H23NO4/c1-2-3-4-5-6-7-8-16-15(20)11-9-12(17)14(19)13(18)10-11/h9-10,17-19H,2-8H2,1H3,(H,16,20)
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n/an/a 2.21E+3n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264600
PNG
(US9718760, C189)
Show SMILES CCCCCCc1ccc(cc1)N(S(=O)(=O)c1ccc(CCC)cc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C27H33NO6S2/c1-3-5-6-7-9-22-10-14-23(15-11-22)28(36(33,34)25-18-19-26(29)27(30)20-25)35(31,32)24-16-12-21(8-4-2)13-17-24/h10-20,29-30H,3-9H2,1-2H3
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n/an/a 2.29E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264622
PNG
(US9718760, C179)
Show SMILES CCCCCCCCN(Cc1cccc(c1)C(F)(F)F)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C22H28F3NO4S/c1-2-3-4-5-6-7-13-26(16-17-9-8-10-18(14-17)22(23,24)25)31(29,30)19-11-12-20(27)21(28)15-19/h8-12,14-15,27-28H,2-7,13,16H2,1H3
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n/an/a 2.40E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264614
PNG
(US9718760, C158)
Show SMILES CCCCCCCCCCCCN(S(=O)(=O)c1ccc(O)c(O)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C24H35NO8S2/c1-2-3-4-5-6-7-8-9-10-11-16-25(34(30,31)19-12-14-21(26)23(28)17-19)35(32,33)20-13-15-22(27)24(29)18-20/h12-15,17-18,26-29H,2-11,16H2,1H3
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n/an/a 2.60E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen


(Bos taurus)
BDBM50286441
PNG
((S)-2-((S)-2-Acetylamino-4-(S)-methyl-pentanoylami...)
Show SMILES CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O
Show InChI InChI=1S/C20H38N6O5/c1-11(2)9-15(24-13(5)27)17(28)26-16(10-12(3)4)18(29)25-14(19(30)31)7-6-8-23-20(21)22/h11-12,14-16H,6-10H2,1-5H3,(H,24,27)(H,25,29)(H,26,28)(H,30,31)(H4,21,22,23)/t14-,15-,16-/m0/s1
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n/an/a 3.70E+3n/an/an/an/an/an/a



University of Arkansas

Curated by ChEMBL


Assay Description
Inhibition of plasmin with Val-L-Leu-L-lysine-p-nitroanilide as substrate


J Med Chem 36: 1084-9 (1993)


BindingDB Entry DOI: 10.7270/Q24F1RCR
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264648
PNG
(US9718760, C161)
Show SMILES CCCCCCCCNC(=O)c1cc(O)c(O)c(O)c1
Show InChI InChI=1S/C15H23NO4/c1-2-3-4-5-6-7-8-16-15(20)11-9-12(17)14(19)13(18)10-11/h9-10,17-19H,2-8H2,1H3,(H,16,20)
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n/an/a 3.70E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264608
PNG
(US9718760, C162)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(CCc1ccccn1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C19H18N2O8S2/c22-16-6-4-14(11-18(16)24)30(26,27)21(10-8-13-3-1-2-9-20-13)31(28,29)15-5-7-17(23)19(25)12-15/h1-7,9,11-12,22-25H,8,10H2
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n/an/a 3.90E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264603
PNG
(US9718760, C224)
Show SMILES CCCCCCCCN(S(=O)(=O)c1ccc(O)cc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C20H27NO7S2/c1-2-3-4-5-6-7-14-21(29(25,26)17-10-8-16(22)9-11-17)30(27,28)18-12-13-19(23)20(24)15-18/h8-13,15,22-24H,2-7,14H2,1H3
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n/an/a 4.34E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264660
PNG
(US9718760, C206)
Show SMILES Oc1ccc(\C=C2/SC(=O)N(Cc3cccc(Br)c3)C2=O)cc1O
Show InChI InChI=1S/C17H12BrNO4S/c18-12-3-1-2-11(6-12)9-19-16(22)15(24-17(19)23)8-10-4-5-13(20)14(21)7-10/h1-8,20-21H,9H2/b15-8-
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n/an/a 4.96E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264626
PNG
(US9718760, C205)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N1CCc2ccccc12
Show InChI InChI=1S/C14H13NO4S/c16-13-6-5-11(9-14(13)17)20(18,19)15-8-7-10-3-1-2-4-12(10)15/h1-6,9,16-17H,7-8H2
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n/an/a 5.05E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264621
PNG
(US9718760, C177)
Show SMILES CCCCCCCCN(Cc1cccc(Cl)c1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C21H28ClNO4S/c1-2-3-4-5-6-7-13-23(16-17-9-8-10-18(22)14-17)28(26,27)19-11-12-20(24)21(25)15-19/h8-12,14-15,24-25H,2-7,13,16H2,1H3
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n/an/a 5.11E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264658
PNG
(US9718760, C199)
Show SMILES Oc1ccc(\C=C2/SC(=O)N(Cc3ccccc3)C2=O)cc1O
Show InChI InChI=1S/C17H13NO4S/c19-13-7-6-12(8-14(13)20)9-15-16(21)18(17(22)23-15)10-11-4-2-1-3-5-11/h1-9,19-20H,10H2/b15-9-
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n/an/a 5.36E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264617
PNG
(US9718760, C170)
Show SMILES CCCCCCCCN(CCCCCCCC)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C22H39NO4S/c1-3-5-7-9-11-13-17-23(18-14-12-10-8-6-4-2)28(26,27)20-15-16-21(24)22(25)19-20/h15-16,19,24-25H,3-14,17-18H2,1-2H3
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n/an/a 5.49E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264620
PNG
(US9718760, C175)
Show SMILES CCCCCCCCN(CC(O)c1ccccc1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C22H31NO5S/c1-2-3-4-5-6-10-15-23(17-22(26)18-11-8-7-9-12-18)29(27,28)19-13-14-20(24)21(25)16-19/h7-9,11-14,16,22,24-26H,2-6,10,15,17H2,1H3
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n/an/a 6.74E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264624
PNG
(US9718760, C186)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N1CCC[C@H]1CCc1ccccc1 |r|
Show InChI InChI=1S/C18H21NO4S/c20-17-11-10-16(13-18(17)21)24(22,23)19-12-4-7-15(19)9-8-14-5-2-1-3-6-14/h1-3,5-6,10-11,13,15,20-21H,4,7-9,12H2/t15-/m0/s1
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n/an/a 6.98E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264608
PNG
(US9718760, C162)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)N(CCc1ccccn1)S(=O)(=O)c1ccc(O)c(O)c1
Show InChI InChI=1S/C19H18N2O8S2/c22-16-6-4-14(11-18(16)24)30(26,27)21(10-8-13-3-1-2-9-20-13)31(28,29)15-5-7-17(23)19(25)12-15/h1-7,9,11-12,22-25H,8,10H2
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n/an/a 7.59E+3n/an/an/an/an/a25



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
PAI-1 inhibitor compounds were dissolved in DMSO to a final concentration of (10-50 mM), depending upon solubility. Compounds were then diluted in ph...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen activator inhibitor 1/Urokinase-type plasminogen activator


(Homo sapiens (Human))
BDBM264629
PNG
(US9718760, C190)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)Nc1ccc(cc1)-c1cccc(F)c1
Show InChI InChI=1S/C18H14FNO4S/c19-14-3-1-2-13(10-14)12-4-6-15(7-5-12)20-25(23,24)16-8-9-17(21)18(22)11-16/h1-11,20-22H
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n/an/a 9.70E+3n/an/an/an/a7.425



THE REGENTS OF THE UNIVERSITY OF MICHIGAN; EASTERN MICHIGAN UNIVERSITY

US Patent


Assay Description
To determine the efficacy of various synthesized compounds as PAI-1 inhibitors, a fluorometric plate assay was carried out to measure the half maxima...


US Patent US9718760 (2017)


BindingDB Entry DOI: 10.7270/Q2K939HK
More data for this
Ligand-Target Pair
Plasminogen


(Bos taurus)
BDBM50046885
PNG
(2-(2-Acetylamino-3-phenyl-propionylamino)-N-(1-for...)
Show SMILES [#6]-[#6](-[#6])-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccccc1)-[#7]-[#6](-[#6])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6]=O |r|
Show InChI InChI=1S/C22H34N6O4/c1-14(2)19(21(32)27-17(13-29)10-7-11-25-22(23)24)28-20(31)18(26-15(3)30)12-16-8-5-4-6-9-16/h4-6,8-9,13-14,17-19H,7,10-12H2,1-3H3,(H,26,30)(H,27,32)(H,28,31)(H4,23,24,25)/t17-,18-,19-/m0/s1
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n/an/a 1.20E+4n/an/an/an/an/an/a



University of Arkansas

Curated by ChEMBL


Assay Description
Inhibition of plasmin with Val-L-Leu-L-lysine-p-nitroanilide as substrate


J Med Chem 36: 1084-9 (1993)


BindingDB Entry DOI: 10.7270/Q24F1RCR
More data for this
Ligand-Target Pair
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