design and synthesis of isosteviol triazole conjugates for cancer therapy

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ID: 172025
2014
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Abstract
One of the keys for successfully developing drugs against the broad spectrum of cancer cell types is structural diversity. In the current study, we focused on a family of isosteviol derivatives as potential novel antitumor agents. Isosteviol is a tetracyclic diterpenoid obtained by acid hydrolysis of steviol glycoside extracts isolated from abundant Stevia rebaudiana plants. In this work, we have designed and synthesized a panel of isosteviol triazole conjugates using “click” chemistry methodology. Evaluation of these compounds against a series of cancer cell lines derived from primary and metastatic tumors demonstrated that these conjugates exhibit cytotoxic activities with IC50 in the low μM range. In addition, their anti-proliferative activities are cancer cell type specific. Taken together, our studies underscore the importance of structural diversity in achieving cancer cell type specific drug development.
Reference Key
khaybullin2014moleculesdesign Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Ravil N. Khaybullin;Mei Zhang;Junjie Fu;Xiao Liang;Tammy Li;Alan R. Katritzky;Paul Okunieff;Xin Qi
Journal Journal of ethnopharmacology
Year 2014
DOI
10.3390/molecules191118676
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