Synthesis, conformation, and biological activity of 14-methoxy Epothilone D

ORGN 457

Jeffrey D. Frein, jfrein@nd.edu and Richard E. Taylor, taylor.61@nd.edu. Department of Chemistry and Biochemistry, Walther Cancer Center, University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, IN 46556
The epothilones are a novel class of microtubule stabilizing anti-cancer natural products which have gained much interest by the synthetic community. Also, rationally designed analogues have met with success in clinical trials, therefore further prompting us to explore the correlation between conformational analysis and biological activity. We have recently shown that C-14 substitution can have a significant effect on conformation and biological activity. The synthesis and biological activity of 14-methoxy epothilone D will be presented.

 

Total Synthesis of Complex Molecules
8:00 AM-12:00 PM, Wednesday, April 9, 2008 Morial Convention Center -- Rm. R05, Oral

Division of Organic Chemistry

The 235th ACS National Meeting, New Orleans, LA, April 6-10, 2008