## Abstract A series of 4β‐[(4‐substituted)‐1,2,3‐triazol‐1‐yl]podophyllotoxin analogues have been synthesized with high regio‐selectivity by employing copper(I)‐catalyzed 1,3‐dipolar cycloaddition of 1‐__O__‐propargyl monosaccharides with C4β‐azido podophyllotoxin and C4β‐azido‐4′‐__O__‐demethyl p
Synthesis and Biological Evaluation of 4β-[(4-Substituted)-1,2,3-triazol-1-yl]podophyllotoxins as Potential Anticancer Agents
✍ Scribed by Pitta Bhaskar Reddy; Satyam Kumar Agrawal; Swaran Singh; Bilal A. Bhat; Ajit K. Saxena; Halmuthur M. Sampath Kumar; Gulam N. Qazi
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 206 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1612-1872
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✦ Synopsis
Abstract
A series of novel 4__β__‐[(4‐substituted)‐1,2,3‐triazol‐1‐yl]podophyllotoxin derivatives were synthesized by employing Cu^I^‐catalyzed click chemistry and evaluated for their anticancer activity against a panel of seven human cancer cell lines (HT‐29, HCT‐15, 502713, HOP‐62, A‐549, MCF‐7, and SF‐295). The compounds 9b, 9c, 9e, 9f, and 9h showed significant cytotoxic activities especially against HT‐29, HCT‐15, 502713 cell lines.
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