| Literature DB >> 22345046 |
Shin-Ichiro Nishimura1, Megumi Hato, Satoshi Hyugaji, Fei Feng, Maho Amano.
Abstract
Inhibited: N-acetylglucosamine (GlcNAc) derivatives with a fluorine atom at the C4 position (2-4) were synthesized, and their ability to inhibit cancer-cell growth was investigated. The administration of these 4F-GlcNAc derivatives to cells led to the unnatural sugar nucleotide 1. Furthermore, N-glycan profiles of cells were determined by using a glycoblotting-based enrichment analysis, which is suitable for high-throughput screenings for drug discovery.Entities:
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Year: 2012 PMID: 22345046 DOI: 10.1002/anie.201108742
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336