Synthesis and AChE inhibitory activity of N -glycosyl benzofuran derivatives

Abstract: Six N-glycosyl benzofuran derivatives were synthesized by the catalysis of organic bases and condensation agents. The benzofuran derivatives were obtained by the reaction of various salicylaldehydes in acetone, and then hydrolyzed to the corresponding carboxylic acids. Finally, the target compounds were synthesized by acylation and the reaction conditions were optimized. The acetylcholinesterase (AChE) inhibitory activity of the desired compounds was tested using Ellman’s method. Most of the compounds showed acetylcholinesterase-inhibition activity; N-(2,4,5-trihydroxy-6-(hydroxymethyl) tetrahydro-2H-pyran-3-yl) benzofuran-2-carbxamide (5a) showed the best acetylcholinesterase inhibition, with an inhibitory rate of 84%.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Synthesis and AChE inhibitory activity of N -glycosyl benzofuran derivatives ; volume:25 ; number:1 ; year:2019 ; pages:162-166 ; extent:5
Heterocyclic communications ; 25, Heft 1 (2019), 162-166 (gesamt 5)

Creator
Wu, Yu-Ran
Ren, Shu-Ting
Wang, Lei
Liu, Xiu-Jian
Wang, You-Xian
Liu, Shu-Hao
Liu, Wei-Wei
Shi, Da-Hua
Cao, Zhi-Ling

DOI
10.1515/hc-2019-0021
URN
urn:nbn:de:101:1-2501140306230.158424151175
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:35 AM CEST

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Associated

  • Wu, Yu-Ran
  • Ren, Shu-Ting
  • Wang, Lei
  • Liu, Xiu-Jian
  • Wang, You-Xian
  • Liu, Shu-Hao
  • Liu, Wei-Wei
  • Shi, Da-Hua
  • Cao, Zhi-Ling

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