Design, synthesis and molecular docking studies of imidazole and benzimidazole linked ethionamide derivatives as inhibitors of InhA and antituberculosis agents-Reference-Cited by-同舟云学术

Design, synthesis and molecular docking studies of imidazole and benzimidazole linked ethionamide derivatives as inhibitors of InhA and antituberculosis agents

Published:2022-03 Issue: Volume:60 Page:128604
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Raghu M.S.,Pradeep Kumar C.B.,Yogesh Kumar K.,Prashanth M.K.,Alshahrani Mohammad Y.,Ahmad Irfan^ORCID,Jain Ranjana

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference35 articles.

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4. Effects of ethionamide and isoxyl on mycolic acid synthesis in Mycobacterium tuberculosis BCG;Winder;J Gen Microbiol,1971

5. Mycolic acid synthesis: a target for ethionamide in mycobacteria;Quemard;Antimicrob Agents Chemother,1992

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