Drupal-Biblio17<style face="normal" font="default" size="100%">Development of a simple assay protocol for high-throughput screening of mycobacterium tuberculosis glutamine synthetase for the identification of novel inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Development of a simple high-throughput screening protocol based on biosynthetic activity of Mycobacterium tuberculosis glutamine synthetase for the identification of novel inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of 11 alpha-substituted bile acid derivatives as potential anti-tuberculosis agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of a focused library of diamino triazines as potential mycobacterium tuberculosis DHFR inhibitors</style>Drupal-Biblio47<style face="normal" font="default" size="100%">Discovery of new chemical entities against diseases of national importance :an HTS approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design, synthesis and biological evaluation of novel azaspiro analogs of linezolid as antibacterial and antitubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of 2-amino-thiophene-tethered ureidopenicillin analogs with potentantibacterial and antitubercular activity</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design, synthesis and biological screening of novel 1,3,4-oxadiazoles as antitubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design, synthesis, and pharmacological evaluation of fluorinated azoles as anti-tubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design, synthesis, docking studies and biological screening of 2-thiazolyl substituted-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazines as potent HIV-1 reverse transcriptase inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of 2-amino-thiophene-proline-conjugates and their anti-tubercular activity against mycobacterium tuberculosis H37Ra</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design, synthesis and biological evaluation of (E)-5-styryl-1,2,4-oxadiazoles as anti-tubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">[DBUH][OAc]-catalyzed domino synthesis of novel benzimidazole incorporated 3,5-Bis (Arylidene)-4-piperidones as potential antitubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Detection of a target protein (GroEl2) in Mycobacterium tuberculosis using a derivative of 1,2,4-triazolethiols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">DNA binding, antitubercular, antibacterial and anticancer studies of newly designed piano-stool ruthenium(ii) complexes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of piano-stool ruthenium(II) complexes and their studies on the inhibition of amyloid ? (1-42) peptide aggregation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design, synthesis, and in vitro biological evaluation of ROS-generating phenanthridin-trione-epoxide conjugates as agents against mycobacterium tuberculosis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">[DBUH][HSO4]-catalyzed solvent-free synthesis of 1,5-benzodiazepine derivatives: bioevaluation and in silico molecular docking study</style>