Pyrrole-Based Hydrazones Synthesized and Evaluated In Vitro as Potential Tuberculostatics

Author(s): Atanas Bijev, Maya Georgieva

Journal Name: Letters in Drug Design & Discovery

Volume 7 , Issue 6 , 2010

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Twelve pyrrole hydrazones were synthesized and evaluated in vitro as inhibitors of Mycobacterium tuberculosis H37Rv with IC50 and IC90 to 5.92 μg/ml and 9.37 μg/ml respectively. The most active 12d (ethyl 5-(4-chlorophenyl)- 2-methyl-1-(4-(2-((5-nitrofuran-2-yl)methylene)hydrazinyl)-4-oxobutyl)-1H-pyrrole-3-carboxylate) has IC90 value of 9.372 μg/ml. The derived second order QSAR model favors moderate molecular surfaces in a combination with electronaccepting substituents in the aromatic hydrazone moiety.

Keywords: Carbohydrazides, Hydrazones, Pyrrole, Synthesis, Tuberculostatics

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Article Details

Year: 2010
Page: [430 - 437]
Pages: 8
DOI: 10.2174/157018010791306588
Price: $65

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