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Updated: Aug 8, 2026

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Structure-Guided Design and Development of Novel Cyclophilin A Inhibitors and Ganoderiol-F Derivatives: An In-Silico Approach
Published on: June 23, 2026
Caulerpenyne-colchicine hybrid: synthesis and biological evaluation
Julien Bourdron1, Laurent Commeiras, Pascale Barbier
1UMR-CNRS 6178 SymBio, équipe Synthèse par voie Organométallique, Université Paul Cézanne (Aix-Marseille III), Marseille, France.
Bioorganic & Medicinal Chemistry
|May 23, 2006
Abstract:
The synthesis of an analog of caulerpenyne having a trimethoxyaryl moiety was achieved in 11% overall yield over 11 steps. Its biological activity has been evaluated as inhibitor of in vitro tubulin polymerization or angiogenesis.

