Reaction Details |
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Target | Cytochrome P450 2C9 |
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Ligand | BDBM50347659 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_756008 (CHEMBL1803984) |
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IC50 | 1200±n/a nM |
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Citation | Katz, JD; Jewell, JP; Guerin, DJ; Lim, J; Dinsmore, CJ; Deshmukh, SV; Pan, BS; Marshall, CG; Lu, W; Altman, MD; Dahlberg, WK; Davis, L; Falcone, D; Gabarda, AE; Hang, G; Hatch, H; Holmes, R; Kunii, K; Lumb, KJ; Lutterbach, B; Mathvink, R; Nazef, N; Patel, SB; Qu, X; Reilly, JF; Rickert, KW; Rosenstein, C; Soisson, SM; Spencer, KB; Szewczak, AA; Walker, D; Wang, W; Young, J; Zeng, Q Discovery of a 5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (MK-2461) inhibitor of c-Met kinase for the treatment of cancer. J Med Chem54:4092-108 (2011) [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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BDBM50347659 |
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n/a |
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Name | BDBM50347659 |
Synonyms: | CHEMBL1802916 | MK-2461 |
Type | Small organic molecule |
Emp. Form. | C24H25N5O5S |
Mol. Mass. | 495.551 |
SMILES | CN(C[C@@H]1COCCO1)S(=O)(=O)Nc1ccc2ccc3ncc(cc3c(=O)c2c1)-c1cnn(C)c1 |r| |
Structure |
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