alexa Caulerpenyne-colchicine hybrid: synthesis and biological evaluation.


Medicinal Chemistry

Author(s): Bourdron J, Commeiras L, Barbier P, BourgarelRey V, Pasquier E,

Abstract Share this page

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

Relevant Expert PPTs

Relevant Speaker PPTs

Recommended Conferences

Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version