Reaction Details |
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Target | Prothrombin |
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Ligand | BDBM254907 |
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Substrate/Competitor | BDBM254912 |
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Meas. Tech. | Inhibition Assay |
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pH | 7.4±n/a |
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Temperature | 295.15±n/a K |
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IC50 | 1.10±n/a nM |
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Comments | extracted |
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Citation | Allerheiligen, S; Buchmüller, A; Engel, K; Gerdes, C; Gericke, KM; Gerisch, M; Heitmeier, S; Hillisch, A; Kinzel, T; Lienau, P; Riedl, B; Röhrig, S; Schmidt, MV; Strassburger, J; Tersteegen, A Substituted benzoxazoles US Patent US9493472 Publication Date 11/15/2016 |
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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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BDBM254907 |
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BDBM254912 |
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Name | BDBM254907 |
Synonyms: | US9493472, 29 | US9493472, 30 | US9493472, 31 |
Type | Small organic molecule |
Emp. Form. | C25H29ClFN3O5 |
Mol. Mass. | 505.966 |
SMILES | CCO[C@@H]1CC(CCO)N(C1)C(=O)c1cc(OC)c2oc(NC(CF)c3cccc(Cl)c3)nc2c1 |r| |
Structure |
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