Author(s): Bourdron J, Commeiras L, Barbier P, BourgarelRey V, Pasquier E,
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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.
This article was published in Bioorg Med Chem
and referenced in Medicinal Chemistry