1. Discovery of novel DprE1 inhibitors via computational bioactivity fingerprints and structure-based virtual screening
- Author
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Dejun Jiang, Tingjun Hou, Yue-Lan Yin, Xueping Hu, Lu Liu, Zhiyong Liu, Tianyu Zhang, Dong-Sheng Cao, Kang-Lin Wan, Xin Chai, Dan Li, Yi-Xuan Lei, Lei Xu, Shah Alam, Liu Yang, Zhe Wang, and Chao Shen
- Subjects
Models, Molecular ,Pharmacology ,Virtual screening ,Oxidase test ,biology ,Molecular model ,Chemistry ,Mycobacterium smegmatis ,Antitubercular Agents ,Mycobacterium tuberculosis ,General Medicine ,biology.organism_classification ,Article ,In vitro ,Mice ,Bacterial Proteins ,Biochemistry ,Animals ,Pharmacology (medical) ,Cytotoxicity ,Mycobacterium - Abstract
Decaprenylphosphoryl-β-D-ribose oxidase (DprE1) plays important roles in the biosynthesis of mycobacterium cell wall. DprE1 inhibitors have shown great potentials in the development of new regimens for tuberculosis (TB) treatment. In this study, an integrated molecular modeling strategy, which combined computational bioactivity fingerprints and structure-based virtual screening, was employed to identify potential DprE1 inhibitors. Two lead compounds (B2 and H3) that could inhibit DprE1 and thus kill Mycobacterium smegmatis in vitro were identified. Moreover, compound H3 showed potent inhibitory activity against Mycobacterium tuberculosis in vitro (MIC(Mtb) = 1.25 μM) and low cytotoxicity against mouse embryo fibroblast NIH-3T3 cells. Our research provided an effective strategy to discover novel anti-TB lead compounds.
- Published
- 2021
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