Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM50442064 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_992750 (CHEMBL2443899) |
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Ki | 12400±n/a nM |
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Citation | de Candia, M; Fiorella, F; Lopopolo, G; Carotti, A; Romano, MR; Lograno, MD; Martel, S; Carrupt, PA; Belviso, BD; Caliandro, R; Altomare, C Synthesis and biological evaluation of direct thrombin inhibitors bearing 4-(piperidin-1-yl)pyridine at the P1 position with potent anticoagulant activity. J Med Chem56:8696-711 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Prothrombin |
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Name: | Prothrombin |
Synonyms: | Activation peptide fragment 1 | Activation peptide fragment 2 | Coagulation factor II | F2 | Prothrombin | THRB_BOVIN | Thrombin | Thrombin heavy chain | Thrombin light chain |
Type: | Enzyme |
Mol. Mass.: | 70502.73 |
Organism: | Bos taurus (Bovine) |
Description: | P00735 |
Residue: | 625 |
Sequence: | MARVRGPRLPGCLALAALFSLVHSQHVFLAHQQASSLLQRARRANKGFLEEVRKGNLERE
CLEEPCSREEAFEALESLSATDAFWAKYTACESARNPREKLNECLEGNCAEGVGMNYRGN
VSVTRSGIECQLWRSRYPHKPEINSTTHPGADLRENFCRNPDGSITGPWCYTTSPTLRRE
ECSVPVCGQDRVTVEVIPRSGGSTTSQSPLLETCVPDRGREYRGRLAVTTSGSRCLAWSS
EQAKALSKDQDFNPAVPLAENFCRNPDGDEEGAWCYVADQPGDFEYCDLNYCEEPVDGDL
GDRLGEDPDPDAAIEGRTSEDHFQPFFNEKTFGAGEADCGLRPLFEKKQVQDQTEKELFE
SYIEGRIVEGQDAEVGLSPWQVMLFRKSPQELLCGASLISDRWVLTAAHCLLYPPWDKNF
TVDDLLVRIGKHSRTRYERKVEKISMLDKIYIHPRYNWKENLDRDIALLKLKRPIELSDY
IHPVCLPDKQTAAKLLHAGFKGRVTGWGNRRETWTTSVAEVQPSVLQVVNLPLVERPVCK
ASTRIRITDNMFCAGYKPGEGKRGDACEGDSGGPFVMKSPYNNRWYQMGIVSWGEGCDRD
GKYGFYTHVFRLKKWIQKVIDRLGS
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BDBM50442064 |
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n/a |
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Name | BDBM50442064 |
Synonyms: | CHEMBL2441028 |
Type | Small organic molecule |
Emp. Form. | C25H26FN3O |
Mol. Mass. | 403.4918 |
SMILES | Fc1cccc(CCc2cccc(NC(=O)C3CCN(CC3)c3ccncc3)c2)c1 |
Structure |
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