Reaction Details |
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Target | Cytochrome P450 2C9 |
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Ligand | BDBM50382412 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_815427 (CHEMBL2027079) |
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IC50 | >10000±n/a nM |
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Citation | Barawkar, DA; Meru, A; Bandyopadhyay, A; Banerjee, A; Deshpande, AM; Athare, C; Koduru, C; Khose, G; Gundu, J; Mahajan, K; Patil, P; Kandalkar, SR; Niranjan, S; Bhosale, S; De, S; Mukhopadhyay, S; Chaudhary, S; Koul, S; Singh, U; Chugh, A; Palle, VP; Mookhtiar, KA; Vacca, J; Chakravarty, PK; Nargund, RP; Wright, SD; Roy, S; Graziano, MP; Singh, SB; Cully, D; Cai, TQ Potent and Selective Inhibitors of Long Chain l-2-Hydroxy Acid Oxidase Reduced Blood Pressure in DOCA Salt-Treated Rats. ACS Med Chem Lett2:919-923 (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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BDBM50382412 |
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n/a |
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Name | BDBM50382412 |
Synonyms: | CHEMBL2022570 |
Type | Small organic molecule |
Emp. Form. | C18H15FN2O2 |
Mol. Mass. | 310.3223 |
SMILES | Cc1[nH]nc(C(O)=O)c1Cc1cccc(c1)-c1ccc(F)cc1 |
Structure |
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