Reaction Details |
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Target | Cytochrome P450 3A4 |
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Ligand | BDBM50128548 |
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Substrate/Competitor | n/a |
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Meas. Tech. | In vitro CYP3A4 Inhibition Assay |
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IC50 | 800±n/a nM |
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Citation | Bareja, SP; Jones, SD; Oblong, JE; Mills, KJ; Bierman, JC Cosmetic compositions containing substituted azole and methods for alleviating the signs of photoaged skin US Patent US9144538 Publication Date 9/29/2015 |
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More Info.: | Get all data from this article, Assay Method |
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Cytochrome P450 3A4 |
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Name: | Cytochrome P450 3A4 |
Synonyms: | Albendazole monooxygenase | Albendazole sulfoxidase | CP3A4_HUMAN | CYP3A3 | CYP3A4 | CYPIIIA3 | CYPIIIA4 | Cytochrome P450 3A3 | Cytochrome P450 3A4 (CYP3A4) | Cytochrome P450 HLp | Nifedipine oxidase | Quinine 3-monooxygenase | Taurochenodeoxycholate 6-alpha-hydroxylase |
Type: | Enzyme |
Mol. Mass.: | 57349.57 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 503 |
Sequence: | MALIPDLAMETWLLLAVSLVLLYLYGTHSHGLFKKLGIPGPTPLPFLGNILSYHKGFCMF
DMECHKKYGKVWGFYDGQQPVLAITDPDMIKTVLVKECYSVFTNRRPFGPVGFMKSAISI
AEDEEWKRLRSLLSPTFTSGKLKEMVPIIAQYGDVLVRNLRREAETGKPVTLKDVFGAYS
MDVITSTSFGVNIDSLNNPQDPFVENTKKLLRFDFLDPFFLSITVFPFLIPILEVLNICV
FPREVTNFLRKSVKRMKESRLEDTQKHRVDFLQLMIDSQNSKETESHKALSDLELVAQSI
IFIFAGYETTSSVLSFIMYELATHPDVQQKLQEEIDAVLPNKAPPTYDTVLQMEYLDMVV
NETLRLFPIAMRLERVCKKDVEINGMFIPKGVVVMIPSYALHRDPKYWTEPEKFLPERFS
KKNKDNIDPYIYTPFGSGPRNCIGMRFALMNMKLALIRVLQNFSFKPCKETQIPLKLSLG
GLLQPEKPVVLKVESRDGTVSGA
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BDBM50128548 |
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n/a |
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Name | BDBM50128548 |
Synonyms: | 1-(1-Biphenyl-4-yl-2-phenyl-methyl)-1H-imidazole | 1-(Biphenyl-4-yl-phenyl-methyl)-1H-imidazole (bifonazole) | 1-(Biphenyl-4-yl-phenyl-methyl)-1H-imidazole( Bifanozole) | 1-(Biphenyl-4-yl-phenyl-methyl)-1H-imidazole(Bifonazole) | 1-(biphenyl-4-yl-phenyl-methyl)-1H-imidazole | BIFONAZOLE | CHEMBL277535 | US9144538, Bifonazole | cid_2378 |
Type | Small organic molecule |
Emp. Form. | C22H18N2 |
Mol. Mass. | 310.3917 |
SMILES | c1cn(cn1)C(c1ccccc1)c1ccc(cc1)-c1ccccc1 |
Structure |
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