Ki Summary

Reaction Details

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Target

Cytochrome P450 3A4

Ligand

BDBM50011134

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_1366300 (CHEMBL3297633)

IC50

23000±n/a nM

Citation

Fader, LD; Carson, R; Morin, S; Bilodeau, F; Chabot, C; Halmos, T; Bailey, MD; Kawai, SH; Coulombe, R; Laplante, S; Mekhssian, K; Jakalian, A; Garneau, M; Duan, J; Mason, SW; Simoneau, B; Fenwick, C; Tsantrizos, Y; Yoakim, C Minimizing the Contribution of Enterohepatic Recirculation to Clearance in Rat for the NCINI Class of Inhibitors of HIV. ACS Med Chem Lett5:711-6 (2014) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

Cytochrome P450 3A4

Name:

Cytochrome P450 3A4

Synonyms:

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

BDBM50011134

n/a

Name

BDBM50011134

Synonyms:

CHEMBL3259907

Type

Small organic molecule

Emp. Form.

C27H26N2O4

Mol. Mass.

442.5063

SMILES

Cc1nc2ccccc2c(-c2ccc3OCCc4ccnc2c34)c1[C@H](OC(C)(C)C)C(O)=O |r,wD:24.29,(15.05,-15.73,;13.72,-14.97,;12.38,-15.74,;11.05,-14.98,;9.71,-15.75,;8.38,-14.98,;8.38,-13.44,;9.71,-12.67,;11.05,-13.43,;12.37,-12.66,;12.36,-11.13,;13.7,-10.35,;13.69,-8.81,;12.35,-8.06,;12.34,-6.52,;11,-5.76,;9.67,-6.54,;9.68,-8.09,;8.37,-8.86,;8.39,-10.39,;9.72,-11.14,;11.03,-10.37,;11.02,-8.84,;13.71,-13.42,;15.04,-12.64,;15.03,-11.1,;16.36,-10.32,;16.35,-8.78,;17.69,-11.09,;17.69,-9.54,;16.38,-13.4,;16.39,-14.94,;17.71,-12.63,)|

Structure