Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM50189311 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1591273 (CHEMBL3829806) |
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Ki | 279±n/a nM |
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Citation | Beckmann, AM; Gilberg, E; Gattner, S; Huang, TL; Vanden Eynde, JJ; Mayence, A; Bajorath, J; Stirnberg, M; Gütschow, M Evaluation of bisbenzamidines as inhibitors for matriptase-2. Bioorg Med Chem Lett26:3741-5 (2016) [PubMed] 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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BDBM50189311 |
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n/a |
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Name | BDBM50189311 |
Synonyms: | 4,4''-(1,2-Phenylenebis(Methylene))Bis(Oxy)Dibenzimidamide | CHEMBL181480 |
Type | Small organic molecule |
Emp. Form. | C22H22N4O2 |
Mol. Mass. | 374.4357 |
SMILES | NC(=N)c1ccc(OCc2ccccc2COc2ccc(cc2)C(N)=N)cc1 |
Structure |
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