Reaction Details |
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Target | Plasminogen activator inhibitor 1 |
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Ligand | BDBM50111273 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_222792 (CHEMBL847120) |
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IC50 | 290±n/a nM |
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Citation | Folkes, A; Brown, SD; Canne, LE; Chan, J; Engelhardt, E; Epshteyn, S; Faint, R; Golec, J; Hanel, A; Kearney, P; Leahy, JW; Mac, M; Matthews, D; Prisbylla, MP; Sanderson, J; Simon, RJ; Tesfai, Z; Vicker, N; Wang, S; Webb, RR; Charlton, P Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1. Bioorg Med Chem Lett12:1063-6 (2002) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Plasminogen activator inhibitor 1 |
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Name: | Plasminogen activator inhibitor 1 |
Synonyms: | Endothelial plasminogen activator inhibitor | PAI | PAI-1 | PAI1 | PAI1_HUMAN | PLANH1 | Plasminogen activator inhibitor 1 | Plasminogen activator inhibitor 1 (PAI-1) | Plasminogen activator inhibitor-1 | Plasminogen activator-1 (PAI-1) | SERPINE1 |
Type: | Enzyme |
Mol. Mass.: | 45064.00 |
Organism: | Homo sapiens (Human) |
Description: | P05121 |
Residue: | 402 |
Sequence: | MQMSPALTCLVLGLALVFGEGSAVHHPPSYVAHLASDFGVRVFQQVAQASKDRNVVFSPY
GVASVLAMLQLTTGGETQQQIQAAMGFKIDDKGMAPALRHLYKELMGPWNKDEISTTDAI
FVQRDLKLVQGFMPHFFRLFRSTVKQVDFSEVERARFIINDWVKTHTKGMISNLLGKGAV
DQLTRLVLVNALYFNGQWKTPFPDSSTHRRLFHKSDGSTVSVPMMAQTNKFNYTEFTTPD
GHYYDILELPYHGDTLSMFIAAPYEKEVPLSALTNILSAQLISHWKGNMTRLPRLLVLPK
FSLETEVDLRKPLENLGMTDMFRQFQADFTSLSDQEPLHVAQALQKVKIEVNESGTVASS
STAVIVSARMAPEEIIMDRPFLFVVRHNPTGTVLFMGQVMEP
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BDBM50111273 |
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n/a |
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Name | BDBM50111273 |
Synonyms: | 6-Benzo[b]thiophen-2-yl-4-hydroxy-2-oxo-1,2-dihydro-quinoline-3-carboxylic acid [4-(7-tetrazol-1-yl-heptyloxy)-phenyl]-amide | CHEMBL10004 |
Type | Small organic molecule |
Emp. Form. | C32H30N6O4S |
Mol. Mass. | 594.683 |
SMILES | Oc1c(C(=O)Nc2ccc(OCCCCCCCn3cnnn3)cc2)c(=O)[nH]c2ccc(cc12)-c1cc2ccccc2s1 |
Structure |
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