Literature DB >> 25950121

Synthesis of pyrrolidine-based analogues of 2-acetamidosugars as N-acetyl-D-glucosaminidase inhibitors.

Anh Tuan Tran1, Bo Luo1, Yerri Jagadeesh2, Nicolas Auberger2, Jérôme Désiré2, Shinpei Nakagawa3, Atsushi Kato3, Yongmin Zhang1, Yves Blériot4, Matthieu Sollogoub5.   

Abstract

A ring-contraction strategy applied to β-azido,γ-hydroxyazepanes yielded after functional group manipulation new tetrahydroxylated pyrrolidines displaying an acetamido moiety, one of these iminosugars demonstrating low micromolar inhibition on N-acetylglucosaminidases.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Glycosidase inhibitors; Iminosugars; Pyrrolidines; Ring-contraction

Mesh:

Substances:

Year:  2015        PMID: 25950121     DOI: 10.1016/j.carres.2015.02.014

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  1 in total

1.  Synthesis of Pyrrolidine Monocyclic Analogues of Pochonicine and Its Stereoisomers: Pursuit ofSimplified Structures and Potent β-N-Acetylhexosaminidase Inhibition.

Authors:  Xin Yan; Yuna Shimadate; Atsushi Kato; Yi-Xian Li; Yue-Mei Jia; George W J Fleet; Chu-Yi Yu
Journal:  Molecules       Date:  2020-03-25       Impact factor: 4.411

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.