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Compile Data Set for Download or QSAR

Found 11 hits of ic50 for UniProtKB: P05121   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
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
PDB

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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/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
PDB

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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/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
PDB

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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 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
PDB

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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 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/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)
PDB

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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/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/Tissue-type plasminogen activator


(Homo sapiens (Human))
BDBM264598
PNG
(US9718760, C155)
Show SMILES CCCCCCCCN(S(=O)(=O)c1cc(F)c(O)c(F)c1)S(=O)(=O)c1cc(F)c(O)c(F)c1
Show InChI InChI=1S/C20H23F4NO6S2/c1-2-3-4-5-6-7-8-25(32(28,29)13-9-15(21)19(26)16(22)10-13)33(30,31)14-11-17(23)20(27)18(24)12-14/h9-12,26-27H,2-8H2,1H3
PDB

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n/an/a 3.48E+4n/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))
BDBM264627
PNG
(US9718760, C160)
Show SMILES Oc1ccc(cc1O)S(=O)(=O)NCc1ccccc1
Show InChI InChI=1S/C13H13NO4S/c15-12-7-6-11(8-13(12)16)19(17,18)14-9-10-4-2-1-3-5-10/h1-8,14-16H,9H2
PDB

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n/an/a 5.82E+4n/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))
BDBM264647
PNG
(US9718760, C156)
Show SMILES CC(C)(C)OC(=O)NCCCOC(=O)c1cc(O)c(O)c(O)c1
Show InChI InChI=1S/C15H21NO7/c1-15(2,3)23-14(21)16-5-4-6-22-13(20)9-7-10(17)12(19)11(18)8-9/h7-8,17-19H,4-6H2,1-3H3,(H,16,21)
PDB

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n/an/a 5.81E+5n/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