Reaction Details |
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Target | Cytochrome P450 2C9 |
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Ligand | BDBM50467108 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1794902 (CHEMBL4267019) |
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IC50 | >20000±n/a nM |
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Citation | Graham, J; Wong, CE; Day, J; McFaddin, E; Ochsner, U; Hoang, T; Young, CL; Ribble, W; DeGroote, MA; Jarvis, T; Sun, X Discovery of benzothiazole amides as potent antimycobacterial agents. Bioorg Med Chem Lett28:3177-3181 (2018) [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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BDBM50467108 |
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n/a |
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Name | BDBM50467108 |
Synonyms: | CHEMBL4292052 |
Type | Small organic molecule |
Emp. Form. | C17H19F3N2OS |
Mol. Mass. | 356.406 |
SMILES | CC1CC(C)CC(C1)C(=O)Nc1nc2ccc(cc2s1)C(F)(F)F |
Structure |
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