Literature DB >> 29427857

Alkynyl and β-ketophosphonates: Selective and potent butyrylcholinesterase inhibitors.

Valeria Cavallaro1, Yanina F Moglie2, Ana P Murray3, Gabriel E Radivoy3.   

Abstract

A series of thirty-three alkynyl and β-ketophosphonates were evaluated for their in vitro acetyl- and butyryl-cholinesterase (AChE and BChE) inhibitory activities using Ellman's spectrophotometric method. None of the examined compounds inhibited AChE activity at tested concentrations while twenty-nine of them showed significant and selective inhibition of BChE with IC50 values between 38.60 µM and 0.04 µM. In addition, structure-activity relationships were discussed. The most effective inhibitors were the dibutyl o-methoxyphenyl alkynylphosphonate 3dc and dibutyl o-methoxyphenyl β-ketophosphonate 4dc. Activities of most potent compounds were also compared with a commercial organophosphorus compound. These results could inspire the design of new inhibitors with stronger activity against BChE.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Butyrylcholinesterase; Enzymatic inhibition; Organophosphorus compounds; Phosphonates

Mesh:

Substances:

Year:  2018        PMID: 29427857     DOI: 10.1016/j.bioorg.2018.01.030

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


  2 in total

1.  Understanding the enzyme-ligand complex: insights from all-atom simulations of butyrylcholinesterase inhibition.

Authors:  Walter Alvarado; Parker Ladd Bremer; Angela Choy; Helen N Dinh; Aingty Eung; Jeannette Gonzalez; Phillippe Ly; Trina Tran; Kensaku Nakayama; Jason P Schwans; Eric J Sorin
Journal:  J Biomol Struct Dyn       Date:  2019-04-07

Review 2.  Recent trends in the direct oxyphosphorylation of C-C multiple bonds.

Authors:  Alireza Bakhtiary; Mohammad Reza Poor Heravi; Akbar Hassanpour; Issa Amini; Esmail Vessally
Journal:  RSC Adv       Date:  2020-12-23       Impact factor: 3.361

  2 in total

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