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.
|
Authors | Shin-Ichiro Nishimura, Megumi Hato, Satoshi Hyugaji, Fei Feng, Maho Amano |
Journal | Angewandte Chemie (International ed. in English)
(Angew Chem Int Ed Engl)
Vol. 51
Issue 14
Pg. 3386-90
(Apr 02 2012)
ISSN: 1521-3773 [Electronic] Germany |
PMID | 22345046
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Chemical References |
- Androgens
- Fluorine
- Acetylglucosamine
|
Topics |
- Acetylglucosamine
(chemical synthesis, chemistry, toxicity)
- Androgens
(metabolism)
- Apoptosis
(drug effects)
- Carbohydrate Sequence
- Cell Line, Tumor
- Drug Evaluation, Preclinical
- Fluorine
(chemistry)
- Glycomics
- Glycosylation
- Humans
- Male
- Molecular Sequence Data
- Prostatic Neoplasms
(metabolism, pathology)
|