期刊
CHEMICAL COMMUNICATIONS
卷 52, 期 20, 页码 3955-3958出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc09289b
关键词
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资金
- King's College London
We report 5-substituted uridine derivatives as novel, uncharged inhibitors of beta-1,4-galactosyltransferase and chemical tools for cellular applications. The new inhibitors reduce P-selectin glycoprotein 1 (PSGL-1) expression in human monocytes. Our results also provide novel insights into a unique mode of glycosyltransferase inhibition.
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