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%.
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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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)
- Urheber
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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
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10.1515/hc-2019-0021
- URN
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urn:nbn:de:101:1-2501140306230.158424151175
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:35 MESZ
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Beteiligte
- 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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