Design and Synthesis of p-hydroxybenzohydrazide Derivatives for their Antimycobacterial Activity
Author:
Publisher
Korean Chemical Society
Subject
Chemical Engineering (miscellaneous),Chemistry (miscellaneous)
Link
http://ocean.kisti.re.kr/downfile/crosscheck/chemical/JAKO201213151421062.pdf
Cited by 7 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. Design, Synthesis and Biological Evaluation of (Z)-1-(Benzo[D]Thiazol-2-yl)-2-(3-Substituted Thiazolidine-4-One) Hydrazine Dpre1 Inhibitors as Antimycobacterial Agents;Pharmaceutical Chemistry Journal;2024-06
2. Hydrazide-hydrazones as Small Molecule Tropomyosin Receptor Kina se A (TRKA) Inhibitors: Synthesis, Anticancer Activities, In silico ADME and Molecular Docking Studies;Medicinal Chemistry;2023-01
3. Synthesis, pharmacokinetic and molecular docking studies of new benzohydrazide derivatives possessing anti-tubercular activity against Mycobacterium tuberculosis H37Rv;Journal of Molecular Structure;2022-02
4. Synthesis of a new series of 2-hydroxy-5-iodo-N’-(1-arylethylidene)benzohydrazides using a deep eutectic solvent as solvent/catalyst under sonication;Heliyon;2019-08
5. Synthesis, In Vivo Anti-Inflammatory Activity, and Molecular Docking Studies of New Isatin Derivatives;International Journal of Medicinal Chemistry;2016-02-14
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