Amphimedosides A-C: synthesis, chemoselective glycosylation, and biological evaluation.

Autor: Langenhan JM; Department of Chemistry, Seattle University, Seattle, Washington 98122, USA. langenha@seattleu.edu, Mullarky E, Rogalsky DK, Rohlfing JR, Tjaden AE, Werner HM, Rozal LM, Loskot SA
Jazyk: angličtina
Zdroj: The Journal of organic chemistry [J Org Chem] 2013 Feb 15; Vol. 78 (4), pp. 1670-6. Date of Electronic Publication: 2013 Feb 07.
DOI: 10.1021/jo302640y
Abstrakt: The amphimedosides, discovered in 2006, are the first examples of naturally occurring glycosylated alkoxyamines. We report syntheses of amphimedosides A-C that feature a stereoselective oxyamine neoglycosylation and found that these alkaloids display modest cytotoxicity toward seven diverse human cancer cell lines, exhibiting IC(50) values ranging from 3.0 μM to greater than 100 μM.
Databáze: MEDLINE