Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM50287154 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_207954 |
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IC50 | 2400±n/a nM |
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Citation | Iwanowicz, EJ; Lau, WF; Lin, J; Roberts, DG; Seiler, SM Derivatives of 5-amidine indole as inhibitors of thrombin catalytic activity Bioorg Med Chem Lett6:1339-1344 (1996) 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 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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BDBM50287154 |
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n/a |
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Name | BDBM50287154 |
Synonyms: | 2-(3-Phenethyl-benzyl)-1H-indole-5-carboxamidine | CHEMBL27758 |
Type | Small organic molecule |
Emp. Form. | C24H23N3 |
Mol. Mass. | 353.4595 |
SMILES | NC(=N)c1ccc2[nH]c(Cc3cccc(CCc4ccccc4)c3)cc2c1 |
Structure |
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