Literature DB >> 14529506

Extending chemoselective ligation to sugar chemistry: convergent assembly of bioactive neoglycoconjugates.

Francesco Peri1.   

Abstract

Glycoproteins and glycolipids play central roles in human health and disease, and their mimetics are primary candidates for drug development. Our understanding of the molecular level of phenomena based on molecular recognition of oligosaccharides by specific receptors has taken tremendous advantage from their chemical synthesis, which provides homogeneous material not attainable from biosynthetic systems. This review summarizes chemoselective approaches for the assembly of neoglycoconjugates. The objective of these methods is to make glycoconjugate synthesis accessible to a broader community, thus accelerating progress in biotechnology.

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Year:  2003        PMID: 14529506     DOI: 10.2174/1389557033487700

Source DB:  PubMed          Journal:  Mini Rev Med Chem        ISSN: 1389-5575            Impact factor:   3.862


  3 in total

1.  Assessment of chemoselective neoglycosylation methods using chlorambucil as a model.

Authors:  Randal D Goff; Jon S Thorson
Journal:  J Med Chem       Date:  2010-10-25       Impact factor: 7.446

2.  Enhancement of cyclopamine via conjugation with nonmetabolic sugars.

Authors:  Randal D Goff; Jon S Thorson
Journal:  Org Lett       Date:  2012-04-27       Impact factor: 6.005

3.  Synthesis and glycosidase inhibitory activity of new hexa-substituted C8-glycomimetics.

Authors:  Olivia Andriuzzi; Christine Gravier-Pelletier; Gildas Bertho; Thierry Prangé; Yves Le Merrer
Journal:  Beilstein J Org Chem       Date:  2005-10-07       Impact factor: 2.883

  3 in total

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