Development of isoniazid–NAD truncated adducts embedding a lipophilic fragment as potential bi-substrate InhA inhibitors and antimycobacterial agents-Reference-Cited by-同舟云学术

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Development of isoniazid–NAD truncated adducts embedding a lipophilic fragment as potential bi-substrate InhA inhibitors and antimycobacterial agents

Published:2010-10 Issue:10 Volume:45 Page:4554-4561
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Delaine Tamara,Bernardes-Génisson Vania,Quémard Annaïk,Constant Patricia,Meunier Bernard,Bernadou Jean

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Cited by 42 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Isatin-pyrimidine hybrid derivatives as enoyl acyl carrier protein reductase (InhA) inhibitors against Mycobacterium tuberculosis;Bioorganic Chemistry;2023-09

2. Anti-tuberculosis drug development via targeting the cell envelope of Mycobacterium tuberculosis;Frontiers in Microbiology;2022-12-21

3. Synthesis and synthetic applications of (4-hydroxyphenyl)perfluoroalkylmethanols;Tetrahedron;2022-01

4. An Overview of the Biological Activity of Pyrrolo[3,4-c]pyridine Derivatives;Pharmaceuticals;2021-04-11

5. Improvement of the novel inhibitor for Mycobacterium enoyl-acyl carrier protein reductase (InhA): a structure–activity relationship study of KES4 assisted by in silico structure-based drug screening;The Journal of Antibiotics;2020-03-09

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