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Updated: May 5, 2026

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Synthesis and Cytotoxicity of Semisynthetic Withalongolide A Analogues
Hashim F Motiwala1, Joseph Bazzill, Abbas Samadi
1Department of Medicinal Chemistry, University of Kansas, Del Shankel Structural Biology Center, 2034 Becker Drive, West Campus, Lawrence, Kansas 66047.
Abstract:
The natural product withaferin A exhibits potent antitumor activity and other diverse pharmacological activities. The recently discovered withalongolide A, a C-19 hydroxylated congener of withaferin A, was recently reported to possess cytotoxic activity against head and neck squamous cell carcinomas. Semisynthetic acetylated analogues of withalongolide A were shown to be considerably more cytotoxic than the parent compound. To further explore the structure-activity relationships, 20 new semisynthetic analogues of withalongolide A were synthesized and evaluated for cytotoxic activity against four different cancer cell lines. A number of derivatives were found to be more potent than the parent compound and withaferin A.
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