Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM50127496 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_208505 (CHEMBL811978) |
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Ki | 440000±n/a nM |
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Citation | Sagi, K; Nakagawa, T; Yamanashi, M; Makino, S; Takahashi, M; Takayanagi, M; Takenaka, K; Suzuki, N; Oono, S; Kataoka, N; Ishikawa, K; Shima, S; Fukuda, Y; Kayahara, T; Takehana, S; Shima, Y; Tashiro, K; Yamamoto, H; Yoshimoto, R; Iwata, S; Tsuji, T; Sakurai, K; Shoji, M Rational design, synthesis, and structure-activity relationships of novel factor Xa inhibitors: (2-substituted-4-amidinophenyl)pyruvic and -propionic acids. J Med Chem46:1845-57 (2003) [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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BDBM50127496 |
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n/a |
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Name | BDBM50127496 |
Synonyms: | CHEMBL51796 | N-[2-(3-Carbamimidoyl-phenoxy)-ethyl]-4-[1-(1-imino-ethyl)-piperidin-4-yloxy]-benzamide |
Type | Small organic molecule |
Emp. Form. | C23H29N5O3 |
Mol. Mass. | 423.5081 |
SMILES | CC(=N)N1CCC(CC1)Oc1ccc(cc1)C(=O)NCCOc1cccc(c1)C(N)=N |
Structure |
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