Synthesis, optimization and structure–activity relationships of 3,5-disubstituted isoxazolines as new anti-tuberculosis agents
- 28 February 2009
- journal article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 44 (2) , 460-472
- https://doi.org/10.1016/j.ejmech.2008.04.007
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Drugs versus bugs: in pursuit of the persistent predator Mycobacterium tuberculosisNature Reviews Microbiology, 2008
- Discovery of novel isoxazolines as anti-tuberculosis agentsBioorganic & Medicinal Chemistry Letters, 2007
- New Tuberculosis Therapeutics: A Growing PipelineThe Journal of Infectious Diseases, 2007
- Synthesis and Antituberculosis Activity of a Novel Series of Optically Active 6-Nitro-2,3-dihydroimidazo[2,1-b]oxazolesJournal of Medicinal Chemistry, 2006
- Synthesis and Evaluation of Cyclic Secondary Amine Substituted Phenyl and Benzyl Nitrofuranyl Amides as Novel Antituberculosis AgentsJournal of Medicinal Chemistry, 2005
- Linezolid for the treatment of multidrug-resistant tuberculosisJournal of Antimicrobial Chemotherapy, 2005
- Synthesis and Evaluation of Nitrofuranylamides as Novel Antituberculosis AgentsJournal of Medicinal Chemistry, 2004
- Combinatorial Lead Optimization of [1,2]-Diamines Based on Ethambutol as Potential Antituberculosis Preclinical CandidatesJournal of Combinatorial Chemistry, 2003
- A Simple Catalytic Method for the Conversion of Aryl Bromides to ArylaminesAngewandte Chemie International Edition in English, 1995
- Picornavirus Inhibitors: Trifluoromethyl Substitution Provides a Global Protective Effect against Hepatic MetabolismJournal of Medicinal Chemistry, 1995