Reaction Details |
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Target | Cytochrome P450 2C9 |
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Ligand | BDBM50433325 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_955733 (CHEMBL2379478) |
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IC50 | 3000±n/a nM |
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Citation | Stammers, TA; Coulombe, R; Rancourt, J; Thavonekham, B; Fazal, G; Goulet, S; Jakalian, A; Wernic, D; Tsantrizos, Y; Poupart, MA; Bös, M; McKercher, G; Thauvette, L; Kukolj, G; Beaulieu, PL Discovery of a novel series of non-nucleoside thumb pocket 2 HCV NS5B polymerase inhibitors. Bioorg Med Chem Lett23:2585-9 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome P450 2C9 |
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Name: | Cytochrome P450 2C9 |
Synonyms: | (R)-limonene 6-monooxygenase | (S)-limonene 6-monooxygenase | CP2C9_HUMAN | CYP2C10 | CYP2C9 | CYPIIC9 | Cytochrome P450 2C9 (CYP2C9 ) | Cytochrome P450 2C9 (CYP2C9) | P-450MP | P450 MP-4/MP-8 | P450 PB-1 | S-mephenytoin 4-hydroxylase |
Type: | Enzyme |
Mol. Mass.: | 55636.33 |
Organism: | Homo sapiens (Human) |
Description: | P11712 |
Residue: | 490 |
Sequence: | MDSLVVLVLCLSCLLLLSLWRQSSGRGKLPPGPTPLPVIGNILQIGIKDISKSLTNLSKV
YGPVFTLYFGLKPIVVLHGYEAVKEALIDLGEEFSGRGIFPLAERANRGFGIVFSNGKKW
KEIRRFSLMTLRNFGMGKRSIEDRVQEEARCLVEELRKTKASPCDPTFILGCAPCNVICS
IIFHKRFDYKDQQFLNLMEKLNENIKILSSPWIQICNNFSPIIDYFPGTHNKLLKNVAFM
KSYILEKVKEHQESMDMNNPQDFIDCFLMKMEKEKHNQPSEFTIESLENTAVDLFGAGTE
TTSTTLRYALLLLLKHPEVTAKVQEEIERVIGRNRSPCMQDRSHMPYTDAVVHEVQRYID
LLPTSLPHAVTCDIKFRNYLIPKGTTILISLTSVLHDNKEFPNPEMFDPHHFLDEGGNFK
KSKYFMPFSAGKRICVGEALAGMELFLFLTSILQNFNLKSLVDPKNLDTTPVVNGFASVP
PFYQLCFIPV
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BDBM50433325 |
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n/a |
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Name | BDBM50433325 |
Synonyms: | CHEMBL2376577 |
Type | Small organic molecule |
Emp. Form. | C20H17NO5S |
Mol. Mass. | 383.418 |
SMILES | Cc1ccc(cc1)S(=O)(=O)Nc1ccc(Oc2ccccc2)cc1C(O)=O |
Structure |
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