Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM50103668 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_208865 |
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IC50 | >10000±n/a nM |
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Citation | Su, T; Wu, Y; Doughan, B; Kane-Maguire, K; Marlowe, CK; Kanter, JP; Woolfrey, J; Huang, B; Wong, P; Sinha, U; Park, G; Malinowski, J; Hollenbach, S; Scarborough, RM; Zhu, BY Design and synthesis of glycolic and mandelic acid derivatives as factor Xa inhibitors. Bioorg Med Chem Lett11:2279-82 (2001) [PubMed] |
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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 precursor | THRB_HUMAN | Thrombin heavy chain | Thrombin light chain |
Type: | Protein |
Mol. Mass.: | 70029.57 |
Organism: | Homo sapiens (Human) |
Description: | P00734 |
Residue: | 622 |
Sequence: | MAHVRGLQLPGCLALAALCSLVHSQHVFLAPQQARSLLQRVRRANTFLEEVRKGNLEREC
VEETCSYEEAFEALESSTATDVFWAKYTACETARTPRDKLAACLEGNCAEGLGTNYRGHV
NITRSGIECQLWRSRYPHKPEINSTTHPGADLQENFCRNPDSSTTGPWCYTTDPTVRRQE
CSIPVCGQDQVTVAMTPRSEGSSVNLSPPLEQCVPDRGQQYQGRLAVTTHGLPCLAWASA
QAKALSKHQDFNSAVQLVENFCRNPDGDEEGVWCYVAGKPGDFGYCDLNYCEEAVEEETG
DGLDEDSDRAIEGRTATSEYQTFFNPRTFGSGEADCGLRPLFEKKSLEDKTERELLESYI
DGRIVEGSDAEIGMSPWQVMLFRKSPQELLCGASLISDRWVLTAAHCLLYPPWDKNFTEN
DLLVRIGKHSRTRYERNIEKISMLEKIYIHPRYNWRENLDRDIALMKLKKPVAFSDYIHP
VCLPDRETAASLLQAGYKGRVTGWGNLKETWTANVGKGQPSVLQVVNLPIVERPVCKDST
RIRITDNMFCAGYKPDEGKRGDACEGDSGGPFVMKSPFNNRWYQMGIVSWGEGCDRDGKY
GFYTHVFRLKKWIQKVIDQFGE
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BDBM50103668 |
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n/a |
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Name | BDBM50103668 |
Synonyms: | 2-(3-Carbamimidoyl-phenoxy)-2-phenyl-N-[4-(3-trifluoromethyl-pyrazol-1-yl)-phenyl]-acetamide | CHEMBL311168 |
Type | Small organic molecule |
Emp. Form. | C25H20F3N5O2 |
Mol. Mass. | 479.4538 |
SMILES | NC(=N)c1cccc(OC(C(=O)Nc2ccc(cc2)-n2ccc(n2)C(F)(F)F)c2ccccc2)c1 |
Structure |
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