Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM50287476 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_208346 (CHEMBL813656) |
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Ki | 0.190000±n/a nM |
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Citation | Steinmetzer, T; Konishi, Y Tripeptidyl pyridinium methyl ketones as potent active site inhibitors of thrombin Bioorg Med Chem Lett6:1677-1682 (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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BDBM50287476 |
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n/a |
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Name | BDBM50287476 |
Synonyms: | 1-((S)-3-{[(S)-1-((R)-2-Amino-3-cyclohexyl-propionyl)-pyrrolidine-2-carbonyl]-amino}-6-guanidino-2-oxo-hexyl)-pyridinium | CHEMBL295863 |
Type | Small organic molecule |
Emp. Form. | C26H42N7O3 |
Mol. Mass. | 500.6562 |
SMILES | N[C@H](CC1CCCCC1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)C[n+]1ccccc1 |
Structure |
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