Reaction Details |
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Target | Genome polyprotein |
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Ligand | BDBM50103864 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_143485 |
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IC50 | 11000±n/a nM |
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Citation | Yeung, KS; Meanwell, NA; Qiu, Z; Hernandez, D; Zhang, S; McPhee, F; Weinheimer, S; Clark, JM; Janc, JW Structure-activity relationship studies of a bisbenzimidazole-based, Zn(2+)-dependent inhibitor of HCV NS3 serine protease. Bioorg Med Chem Lett11:2355-9 (2001) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Genome polyprotein |
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Name: | Genome polyprotein |
Synonyms: | Hepatitis C virus NS3 protease/helicase | Hepatitis C virus serine protease, NS3/NS4A |
Type: | Protein |
Mol. Mass.: | 67067.41 |
Organism: | Hepatitis C virus |
Description: | A3EZI9 |
Residue: | 631 |
Sequence: | APITAYAQQTRGLLGCIITSLTGRDKNQVEGEVQIVSTAAQTFLATCINGVCWTVYHGAG
TRTIASSKGPVIQMYTNVDQDLVGWPAPQGARSLTPCTCGSSDLYLVTRHADVIPVRRRG
DGRGSLLSPRPISYLKGSSGGPLLCPAGHAVGIFRAAVCTRGVAKAVDFIPVEGLETTMR
SPVFSDNSSPPAVPQSYQVAHLHAPTGSGKSTKVPAAYAAQGYKVLVLNPSVAATLGFGA
YMSKAHGIDPNIRTGVRTITTGSPITYSTYGKFLADGGCSGGAYDIIICDECHSTDATSI
LGIGTVLDQAETAGARLTVLATATPPGSVTVPHPNIEEVALSTTGEIPFYGKAIPLEAIK
GGRHLIFCHSKKKCDELAAKLVALGVNAVAYYRGLDVSVIPASGDVVVVATDALMTGFTG
DFDSVIDCNTCVTQTVDFSLDPTFTIETTTLPQDAVSRTQRRGRTGRGKPGIYRFVTPGE
RPSGMFDSSVLCECYDAGCAWYELTPAETTVRLRAYMNTPGLPVCQDHLEFWEGVFTGLT
HIDAHFLSQTKQSGENLPYLVAYQATVCARAQAPPPSWDQMWKCLIRLKPTLHGPTPLLY
RLGAVQNEITLTHPITKYIMTCMSADLEVVT
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BDBM50103864 |
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n/a |
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Name | BDBM50103864 |
Synonyms: | 2-(3-{[2-(1H-Benzoimidazol-2-ylmethyl)-3-methyl-3H-benzoimidazole-5-carbonyl]-amino}-3-carboxy-propionylsulfamoyl)-benzoic acid methyl ester | CHEMBL310787 |
Type | Small organic molecule |
Emp. Form. | C29H26N6O8S |
Mol. Mass. | 618.617 |
SMILES | COC(=O)c1ccccc1S(=O)(=O)NC(=O)CC(NC(=O)c1ccc2nc(Cc3nc4ccccc4[nH]3)n(C)c2c1)C(O)=O |
Structure |
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