Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM50070633 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_208901 |
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Ki | 180±n/a nM |
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Citation | Weber, IR; Neidlein, R; von der Saal, W; Grams, F; Leinert, H; Strein, K; Engh, RA; Kucznierz, R Diarylsulfonamides as selective, non-peptidic thrombin inhibitors. Bioorg Med Chem Lett8:1613-8 (1999) [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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BDBM50070633 |
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n/a |
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Name | BDBM50070633 |
Synonyms: | CHEMBL289790 | N-[3-(4-Guanidino-butoxy)-5-methyl-phenyl]-benzenesulfonamide |
Type | Small organic molecule |
Emp. Form. | C18H24N4O3S |
Mol. Mass. | 376.473 |
SMILES | Cc1cc(NS(=O)(=O)c2ccccc2)cc(OCCCCNC(N)=N)c1 |
Structure |
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