Synthesis and antituberculosis activity of new hydrazide derivatives

Archiv der Pharmazie
Zafer Asim KaplancikliJean-Claude Teulade

Abstract

The increasing clinical importance of drug-resistant mycobacterial pathogens, especially Mycobacterium tuberculosis, has lent additional urgency to microbiological research and new antimycobacterial compound development. For this purpose, new hydrazide derivatives of imidazo[1,2-a]pyridine were synthesized and evaluated for antituberculosis activity. The reaction of 2-[(2-carboxyimidazo[1,2-a]pyridine-3-yl)sulfanyl]acetic acid hydrazide with various benzaldehydes gave N-(arylidene)-2-[(2-carboxyimidazo[1,2-a]pyridine-3-yl)sulfanyl]acetic acid hydrazide derivatives. The chemical structures of the compounds were elucidated by IR,(1)H-NMR, FAB-MS spectral data and elemental analysis. Antituberculosis activities of the synthesized compounds were determined by broth microdilution assay, the Microplate Alamar Blue Assay in BACTEC 12B medium. The results were screened in vitro, using the BACTEC 460 Radiometric System against Mycobacterium tuberculosis H37Rv (ATCC 27294) at 6.25 microg/mL; the tested compounds showed significant inhibition.

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Citations

Sep 16, 2015·Zeitschrift Für Naturforschung. C, a Journal of Biosciences·Begüm Evranos-AksözSelda Özgen Özgacar
Mar 9, 2017·Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry·Sandeep Kumar Mishra, N Suryaprakash

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