| Literature DB >> 29638128 |
Mohammed Y R Sardar1,2, Appi Reddy Mandhapati1,2, Simon Park1,2, Walter J Wever1,2, Richard D Cummings1, Elliot L Chaikof1,2,3.
Abstract
Selectins are a class of cell adhesion molecules that play a critical role during the initial steps of inflammation. The N-terminal domain of P-selectin glycoprotein ligand-1 (PSGL-1) binds to all selectins, but with the highest affinity to P-selectin. Recent evidence suggests that the blockade of P-selectin/PSGL-1 interactions provides a viable therapeutic option for the treatment of many inflammatory diseases. Herein, we report the total synthesis of threonine bearing sialyl LewisX (sLeX) linked to a Core-1- O-hexasaccharide 1, as a key glycan of the N-terminal domain of PSGL-1. A convergent synthesis using α-selective sialylation and a regioselective [4+2] glycosylation are the key features of this synthesis.Entities:
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Year: 2018 PMID: 29638128 PMCID: PMC7648531 DOI: 10.1021/acs.joc.7b03117
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354