Literature DB >> 33548731

Multivalent butyrylcholinesterase inhibitor discovered by exploiting dynamic combinatorial chemistry.

Shuang Zhao1, Jintao Xu1, Shixin Zhang1, Maochun Han1, Yao Wu1, Yusi Li1, Lei Hu2.   

Abstract

In this study, we report the generation of a polymer-based dynamic combinatorial library (DCL) incorporating exchangeable side chains using acylhydrazone formation reaction. In combination with tetrameric butyrylcholinesterase (BChE), the most potent binding side chain was identified, and the information obtained was further used for the synthesis of a multivalent BChE inhibitor. In the in vitro biological evaluation, this multivalent inhibitor exhibited not only better inhibitory effect than the commercial reference but also high selectivity on BChE over acetylcholinesterase (AChE).
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Butyrylcholinesterase; Dynamic combinatorial chemistry; Macromolecule; Multivalent interaction; Protein inhibition

Year:  2021        PMID: 33548731     DOI: 10.1016/j.bioorg.2021.104656

Source DB:  PubMed          Journal:  Bioorg Chem        ISSN: 0045-2068            Impact factor:   5.275


  1 in total

1.  Development of tacrine clusters as positively cooperative systems for the inhibition of acetylcholinesterase.

Authors:  Tereza Cristina Santos Evangelista; Óscar López; Sabrina Baptista Ferreira; José G Fernández-Bolaños; Magne O Sydnes; Emil Lindbäck
Journal:  J Enzyme Inhib Med Chem       Date:  2021-12       Impact factor: 5.051

  1 in total

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