Synthesis of a Benzene-containing C1-Phosphonate Analogue of UDP-GlcNAc for the Inhibition ofO-GlcNAc Transferase-Reference-Cited by-同舟云学术

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Synthesis of a Benzene-containing C1-Phosphonate Analogue of UDP-GlcNAc for the Inhibition ofO-GlcNAc Transferase

Published:2015-12-17 Issue:1 Volume:37 Page:7-12
ISSN:1229-5949
Container-title:Bulletin of the Korean Chemical Society
language:en
Short-container-title:Bull. Korean Chem. Soc.

Author:

Im Jungkyun¹

Affiliation:

1. Department of Nanochemical Engineering; Soonchunhyang University; Asan 336-745 Korea

Funder

Soonchunhyang University Research Fund

Industry Technology R&D Program of MOTIE/KEIT

Publisher

Wiley

Subject

General Chemistry

Reference36 articles.

1. Synergy of Peptide and Sugar in O-GlcNAcase Substrate Recognition

2. Cycling of O-linked β-N-acetylglucosamine on nucleocytoplasmic proteins

3. Site-specific interplay between O-GlcNAcylation and phosphorylation in cellular regulation

4. Glycosylation of the Nuclear Pore

5. O-GlcNAc Modification Is an Endogenous Inhibitor of the Proteasome

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Structure-based design of bacterial transglycosylase inhibitors incorporating biphenyl, amine linker and 2-alkoxy-3-phosphorylpropanoate moieties;European Journal of Medicinal Chemistry;2018-04

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