Reaction Details |
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Target | RNA-directed RNA polymerase |
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Ligand | BDBM50181689 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_331786 (CHEMBL864669) |
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IC50 | 3000±n/a nM |
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Citation | Powers, JP; Piper, DE; Li, Y; Mayorga, V; Anzola, J; Chen, JM; Jaen, JC; Lee, G; Liu, J; Peterson, MG; Tonn, GR; Ye, Q; Walker, NP; Wang, Z SAR and mode of action of novel non-nucleoside inhibitors of hepatitis C NS5b RNA polymerase. J Med Chem49:1034-46 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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RNA-directed RNA polymerase |
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Name: | RNA-directed RNA polymerase |
Synonyms: | Hepatitis C virus NS5B RNA-dependent RNA polymerase | NS5B protein |
Type: | Protein |
Mol. Mass.: | 25173.95 |
Organism: | Hepatitis C virus |
Description: | Q8JXU8 |
Residue: | 229 |
Sequence: | RTEEAIYQCCDLDPQARVAIRSLTERLYVGGPLTNSRGENCGYRRRASGVLTTSCGNTLT
CYIKAQAACRAAGRQDCTMLVCGDDLVVICESAGVQEDAASLRAFTEAMTRYSAPPGDPP
QPEYDLELITSCSSNVSVAHDGAGKRVYYLTRDPTTPLARAAWETARHTPVNSWLGNIIM
FAPTLWVRMIMLTHFFSVLIARDQLEQALDCEIYGACYSIEPLLPPIIQ
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BDBM50181689 |
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n/a |
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Name | BDBM50181689 |
Synonyms: | 5-(2,4-difluorobenzylidene)-3-(benzenesulfonylamino)-4-oxo-2-thionothiazolidine | CHEMBL200986 |
Type | Small organic molecule |
Emp. Form. | C16H10F2N2O3S3 |
Mol. Mass. | 412.454 |
SMILES | Fc1ccc(C=C2SC(=S)N(NS(=O)(=O)c3ccccc3)C2=O)c(F)c1 |w:5.4| |
Structure |
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