Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377139 | Bioorganic & Medicinal Chemistry Letters | 2007 | 6 Pages |
Abstract
4-Amino analogues prepared from β-boswellic acid and 11-keto-β-boswellic acid, wherein the carboxyl group in ursane nucleus was replaced by an amino function via Curtius reaction, displayed improved cytotoxicity than the parent molecules. The same molecules also exhibited apoptotic activity by inducing DNA fragmentation.
Graphical abstractSemi-synthetic 3-hydroxy-4-amino analogues prepared from boswellic acids, replacing carboxylic acid by an amino function, exhibited improved cytotoxicity as well as apoptotic activity.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bhahwal A. Shah, Ajay Kumar, Pankaj Gupta, Madhunika Sharma, Vijay K. Sethi, Ajit K. Saxena, Jaswant Singh, Ghulam N. Qazi, Subhash C. Taneja,