Rationalization of physicochemical characters of oxazolyl thiosemicarbazone analogs towards multi-drug resistant tuberculosis: A QSAR approach
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Pharmacology,General Medicine
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1. The potential impact of structural genomics on tuberculosis drug discovery
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1. Synthesis, Crystal Structure, and Antibacterial Activity of Four Novel Oxazolyl Acylhydrazones;Crystallography Reports;2022-12
2. Synthesis, Characterization and in vitro Antimicrobial Screening of Some Novel Series of 2-Azetidinone Derivatives Integrated with Quinoline, Pyrazole and Benzofuran Moieties;Asian Journal of Chemistry;2020-02-25
3. 2D QSAR Analysis of Substituted Quinoxalines for their Antitubercular and Antileptospiral Activities;Current Computer-Aided Drug Design;2019-03-12
4. 3D QSAR study of 4H-chromen-1,2,3,4-tetrahydropyrimidine-5-carboxylate derivatives as potential anti-mycobacterial agents;Medicinal Chemistry Research;2013-11-28
5. Synthesis, antimycobacterial and anticancer activity of novel indole-based thiosemicarbazones;Archives of Pharmacal Research;2013-09-24
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