Syntheses of lipophilic chalcones and their conformationally restricted analogues as antitubercular agents

Syntheses of lipophilic chalcones and their conformationally restricted analogues as antitubercular agents Synthesis and in vitro evaluation of substituted 3-cinnamoyl-4-hydroxy-pyran-2-one (CHP) in pursuit of new potential antituberculosis agents QSAR-driven design, synthesis and discovery of potent chalcone derivatives with antitubercular activity Synthesis and structure-activity relationship of new chalcone linked 5-phenyl-3-isoxazolecarboxylic acid methyl esters potentially active against drug resistant Mycobacterium tuberculosis Synthesis and evaluation of new chalcones, derived pyrazoline and cyclohexenone derivatives as potent antimicrobial, antitubercular and antileishmanial agents Synthesis and evaluation of anti-tubercular activity of 6-(4-substitutedpiperazin-1-yl) phenanthridine analogues Indole chalcones: Design, synthesis, in vitro and in silico evaluation against Mycobacterium tuberculosis Synthesis of novel 3-cyclohexylpropanoic acid-derived nitrogen heterocyclic compounds and their evaluation for tuberculostatic activity 1-Chloro-2-formyl indenes and tetralenes as antitubercular agents Synthesis and antitubercular activity of 7-chloro-4-quinolinylhydrazones derivatives