Literature DB >> 23368752

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

Joseph M Langenhan1, Edouard Mullarky, Derek K Rogalsky, James R Rohlfing, Anja E Tjaden, Halina M Werner, Leonardo M Rozal, Steven A Loskot.   

Abstract

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.

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Year:  2013        PMID: 23368752     DOI: 10.1021/jo302640y

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Synthesis and antibacterial activity of doxycycline neoglycosides.

Authors:  Jianjun Zhang; Larissa V Ponomareva; Karen Marchillo; Maoquan Zhou; David R Andes; Jon S Thorson
Journal:  J Nat Prod       Date:  2013-08-29       Impact factor: 4.050

2.  The identification of perillyl alcohol glycosides with improved antiproliferative activity.

Authors:  Nitin S Nandurkar; Jianjun Zhang; Qing Ye; Larissa V Ponomareva; Qing-Bai She; Jon S Thorson
Journal:  J Med Chem       Date:  2014-08-25       Impact factor: 7.446

3.  Development of a multifunctional aminoxy-based fluorescent linker for glycan immobilization and analysis.

Authors:  Carmen Jiménez-Castells; Rhiannon Stanton; Shi Yan; Paul Kosma; Iain Bh Wilson
Journal:  Glycobiology       Date:  2016-05-24       Impact factor: 4.313

  3 in total

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