Structure-activity relationships within a family of selectively cytotoxic macrolide natural products.

Authors

Salomon, A R; Zhang, Y; Seto, H; Khosla, C

Publication Year 2001
Journal Organic Letters
Chapter
Pages 57-59
Volume 3
Issue 1
Issn
Isbn
PMID 11429871.0
PMCID
DOI 10.1021/ol006767d
URL http://dx.doi.org/10.1021/ol006767d

[figure: see text] We describe a semi-synthetic deglycosylated derivative of apoptolidin that retains considerable activity against the mitochondrial ATPase but has greatly reduced cellular cytotoxicity. We also demonstrate that a related antifungal natural product, cytovaricin, inhibits the same molecular target. Structural comparison of these macrolides provides insights into their conserved features that are presumably important for biological activity and identifies promising avenues at the interface of organic synthesis and biosynthesis for the generation of new selective cytotoxic agents.