Reaction Details 
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Cytochrome P450 3A4
Ligand
BDBM50536193
Substrate
n/a
Meas. Tech.
ChEMBL_1933089 (CHEMBL4478741)
IC50
100±n/a nM
Citation
Norcross, NR; Baragaña, B; Wilson, C; Hallyburton, I; Osuna-Cabello, M; Norval, S; Riley, J; Stojanovski, L; Simeons, FR; Porzelle, A; Grimaldi, R; Wittlin, S; Duffy, S; Avery, VM; Meister, S; Sanz, L; Jiménez-Díaz, B; Angulo-Barturen, I; Ferrer, S; Martínez, MS; Gamo, FJ; Frearson, JA; Gray, DW; Fairlamb, AH; Winzeler, EA; Waterson, D; Campbell, SF; Willis, P; Read, KD; Gilbert, IH Trisubstituted Pyrimidines as Efficacious and Fast-Acting Antimalarials. J Med Chem 59:6101-20 (2016) [PubMed] ArticleMore Info.:
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:
BDBM50536193
Synonyms:
CHEMBL548646 | GNF-Pf-1447 | TCMDC-125419
Type:
Small organic molecule
Emp. Form.:
C23H19N5
Mol. Mass.:
365.4305
SMILES:
C1Cc2ccccc2CN1c1cc(nc(n1)-c1ccncc1)-c1cccnc1
Structure:
