Article ID Journal Published Year Pages File Type
1378918 Bioorganic & Medicinal Chemistry Letters 2005 5 Pages PDF
Abstract

As a part of an ongoing search for new isoniazid-related isonicotinoylhydrazones (ISNEs), 2′-monosubstituted isonicotinohydrazides and cyanoboranes, some analogues belonging to these three series of compounds were further evaluated in an in vitro advanced antimycobacterial screening. The results here reported allowed us to extend their structure–activity relationships. A general correlation emerged between their lipophilicity and effectiveness against intracellular M. tuberculosis. On the whole, the most interesting result of this research was that some hydrazides and ISNEs proved to be more effective antimycobacterial agents than parental isoniazid in a TB-infected macrophage model.

Graphical abstractThe in vitro antimycobacterial activities of some isoniazid derivatives are reported.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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