Reaction Details |
| Report a problem with these data |
Target | Prothrombin |
---|
Ligand | BDBM12589 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_553539 (CHEMBL958722) |
---|
IC50 | 4±n/a nM |
---|
Citation | Congreve, M; Chessari, G; Tisi, D; Woodhead, AJ Recent developments in fragment-based drug discovery. J Med Chem51:3661-80 (2008) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Prothrombin |
---|
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
|
|
|
BDBM12589 |
---|
n/a |
---|
Name | BDBM12589 |
Synonyms: | (2R,3S)-3-({[5-chloro-2-(1H-1,2,3,4-tetrazol-1-yl)phenyl]methyl}amino)-2-hydroxy-N-(4-methoxyphenyl)-4-phenylbutane-1-sulfonamido | CHEMBL203590 | N-((2R,3S)-3-{[5-chloro-2-(1H-tetrazol-1-yl)benzyl]amino}-2-hydroxy-4-phenylbutyl)-4-methoxybenzenesulfonamide | benzenesulfonamide-chlorophenyl hybrid compound 7 |
Type | Small organic molecule |
Emp. Form. | C25H27ClN6O4S |
Mol. Mass. | 543.038 |
SMILES | COc1ccc(cc1)S(=O)(=O)NC[C@@H](O)[C@H](Cc1ccccc1)NCc1cc(Cl)ccc1-n1cnnn1 |r| |
Structure |
|