[Design, synthesis and evaluation of N-acyl-4-phenylthiazole-2-amines as acetylcholinesterase inhibitors]

Yao Xue Xue Bao. 2014 Jun;49(6):813-8.
[Article in Chinese]

Abstract

N-Acyl-4-phenylthiazole-2-amines were designed and synthesized, moreover their effects on acetylcholinesterase activities were tested. N-Acyl-4-phenylthiazole-2-amines were prepared from substituted 2-bromo-1-acetophenones by three steps reaction, and their AChE inhibitory activities were measured by Ellman method in vitro. The results showed that the target compounds had a certain inhibitory activity on AChE in vitro. Among them, 8c was the best, and IC50 of 8c was 0.51 micromol x L(-1), better than that of rivastigmine and Huperzine-A. The inhibitory activities of N-acyl-4-phenylthiazole-2-amines on acetylcholinesterase are worth while to be further studied.

MeSH terms

  • Acetylcholinesterase / metabolism
  • Alkaloids / pharmacology
  • Amines / chemical synthesis
  • Amines / pharmacology*
  • Cholinesterase Inhibitors / chemical synthesis
  • Cholinesterase Inhibitors / pharmacology*
  • Drug Design*
  • Rivastigmine / pharmacology
  • Sesquiterpenes / pharmacology
  • Structure-Activity Relationship
  • Thiazoles / pharmacology*

Substances

  • Alkaloids
  • Amines
  • Cholinesterase Inhibitors
  • Sesquiterpenes
  • Thiazoles
  • huperzine A
  • Acetylcholinesterase
  • Rivastigmine