Drug intelligence / Profile preview

N-[(13-CYCLOHEXYL-6,7-DIHYDROINDOLO[1,2-D][1,4]BENZOXAZEPIN-10-YL)CARBONYL]-2-METHYL-L-ALANINE

Development stage
Preclinical
Lead developer
Japan Tobacco
Modality
Small Molecules
Administration
Oral
01

Overview

N-[(13-CYCLOHEXYL-6,7-DIHYDROINDOLO[1,2-D][1,4]BENZOXAZEPIN-10-YL)CARBONYL]-2-METHYL-L-ALANINE is an experimental small molecule non-nucleoside inhibitor (NNI) of the Hepatitis C Virus (HCV) NS5B RNA-dependent RNA polymerase. Developed by Bristol Myers Squibb, it served as a key lead compound in the indolo-benzoxazepine series that eventually produced the clinical candidate beclabuvir (BMS-791325). The compound binds to the allosteric thumb site 1 of the NS5B polymerase, inducing conformational changes that inhibit the initiation of viral RNA synthesis. It has been extensively utilized in structural biology research, including X-ray crystallography studies (e.g., PDB 3SKE), to elucidate the binding mechanisms and structure-activity relationships of this chemical class against various HCV genotypes.

Other names
DB08031DB-08031DB 08031Compound 1Compound1Compound-1N-[(13-cyclohexyl-6,7-dihydroindolo[1,2-d][1,4]benzoxazepin-10-yl)carbonyl]-2-methylalanine
02

Targets

NFE2L2 (Nuclear factor (erythroid-derived 2)-like 2)

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