Literature DB >> 1804569

A new class of potent antiproliferative glycolipids.

S Adam1, F Kaufmann.   

Abstract

The synthesis and biological activities of a new class of antiproliferative glycolipids with an unexpected broad spectrum of activity, including a human multidrug resistant cell line, are described. Chemically these compounds are glycolipids derived from N-acetyl-D-glucosamine and glycyrrhetinic acid (beta-aglycone). Peptidation of the glucoacids allyl 3 beta-[[2-acetamido-3-O-[(R)-1-carboxyethyl]- 2-deoxy-4,6-O-isopropylidene-beta-D-glucopyranosyl]oxy]-11-oxo-12- oleanen-30-oate and (R,S)-2-methoxy-3-(octadecyloxy)propyl-2-acetamido-3-O-[(R)-1-carb oxyethyl]- 2-deoxy-4,6-O-isopropylidene-beta-D-glucopyranoside was successfully achieved after activation with O-benzotriazolyl-N,N,N',N' -tetramethyluronium hexafluorophosphate.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1804569     DOI: 10.1016/0009-3084(91)90025-7

Source DB:  PubMed          Journal:  Chem Phys Lipids        ISSN: 0009-3084            Impact factor:   3.329


  1 in total

1.  Synthesis of novel 6-triazologlycolipids via click chemistry and their preliminary cytotoxicity assessments.

Authors:  Hai-Lin Zhang; Xiao-Peng He; Li Sheng; Yuan Yao; Wei Zhang; Xiao-Xin Shi; Jia Li; Guo-Rong Chen
Journal:  Mol Divers       Date:  2011-06-05       Impact factor: 2.943

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.