19 articles for thisTarget
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Synthesis, characterization and antitubercular activities of novel pyrrolyl hydrazones and their Cu-complexes.
S.E.T'S College Of Pharmacy
Piperazine derivatives: synthesis, inhibition of the Mycobacterium tuberculosis enoyl-acyl carrier protein reductase and SAR studies.
Pontif£Cia Universidade Cat£Lica Do Rio Grande Do Sul
Development of benzo[d]oxazol-2(3H)-ones derivatives as novel inhibitors of Mycobacterium tuberculosis InhA.
Birla Institute Of Technology
Diarylthiazole: an antimycobacterial scaffold potentially targeting PrrB-PrrA two-component system.
Astrazeneca
2-Phenylindole and Arylsulphonamide: Novel Scaffolds Bactericidal against Mycobacterium tuberculosis.
Astrazeneca
Development of 2-(4-oxoquinazolin-3(4H)-yl)acetamide derivatives as novel enoyl-acyl carrier protein reductase (InhA) inhibitors for the treatment of tuberculosis.
Birla Institute Of Technology
Encoded library technology as a source of hits for the discovery and lead optimization of a potent and selective class of bactericidal direct inhibitors of Mycobacterium tuberculosis InhA.
Glaxosmithkline
Methyl-thiazoles: a novel mode of inhibition with the potential to develop novel inhibitors targeting InhA in Mycobacterium tuberculosis.
Astrazeneca India
Identification of novel antimycobacterial chemical agents through the in silico multi-conformational structure-based drug screening of a large-scale chemical library.
Kyushu Institute Of Technology
Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agents.
Cnrs
Synthesis and in vitro antimycobacterial activity of B-ring modified diaryl ether InhA inhibitors.
Stony Brook University
2-Hexadecynoic acid inhibits plasmodial FAS-II enzymes and arrests erythrocytic and liver stage Plasmodium infections.
University Of London
Discovery of potential new InhA direct inhibitors based on pharmacophore and 3D-QSAR analysis followed by in silico screening.
China Pharmaceutical University
Natural products, small molecules, and genetics in tuberculosis drug development.
National Institute Of Diabetes And Digestive And Kidney Diseases
Agonodepsides a and B: two new depsides from a filamentous fungus F7524.
Institute Of Molecular And Cell Biology
Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis.
University Of Minnesota