Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1396296 | European Journal of Medicinal Chemistry | 2010 | 9 Pages |
Abstract
Designed novel imidazo[1,2-a]pyrazine based inhibitors, synthesized by condensing α-aminopyrazines with α-halocarbonyl compounds followed by electrophilic substitutions. Cytotoxic effects on four cancer cell lines evaluated. Based on preliminary data, imidazo[1,2-a]pyrazine template redesigned to improve activity.
Graphical abstractDesign, synthesis and evaluation of imidazo[1,2-a]pyrazine derivatives, by systematically varying substitutions, to establish SAR for cytotoxic activity against cancer cell lines, MDA-MB-231, MCF-7, SK-N-SH and Hep G2, reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shailaja Myadaraboina, Manjula Alla, Venkateshwarlu Saddanapu, Vittal Rao Bommena, Anthony Addlagatta,