Reaction Details Report a problem with these data
Target
Cytochrome P450 3A4
Ligand
BDBM50128548
Substrate
n/a
Meas. Tech.
In vitro CYP3A4 Inhibition Assay
IC50
800±n/a nM
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 
Target
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:
MALIPDLAMETWLLLAVSLVLLYLYGTHSHGLFKKLGIPGPTPLPFLGNILSYHKGFCMFDMECHKKYGKVWGFYDGQQPVLAITDPDMIKTVLVKECYSVFTNRRPFGPVGFMKSAISIAEDEEWKRLRSLLSPTFTSGKLKEMVPIIAQYGDVLVRNLRREAETGKPVTLKDVFGAYSMDVITSTSFGVNIDSLNNPQDPFVENTKKLLRFDFLDPFFLSITVFPFLIPILEVLNICVFPREVTNFLRKSVKRMKESRLEDTQKHRVDFLQLMIDSQNSKETESHKALSDLELVAQSIIFIFAGYETTSSVLSFIMYELATHPDVQQKLQEEIDAVLPNKAPPTYDTVLQMEYLDMVVNETLRLFPIAMRLERVCKKDVEINGMFIPKGVVVMIPSYALHRDPKYWTEPEKFLPERFSKKNKDNIDPYIYTPFGSGPRNCIGMRFALMNMKLALIRVLQNFSFKPCKETQIPLKLSLGGLLQPEKPVVLKVESRDGTVSGA
  
Inhibitor
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:
Search PDB for entries with ligand similarity: