» Articles » PMID: 11374978

Coumarins Isolated from Angelica Gigas Inhibit Acetylcholinesterase: Structure-activity Relationships

Overview
Journal J Nat Prod
Date 2001 May 26
PMID 11374978
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Acetylcholinesterase (AChE) inhibitory activity-guided fractionation of Angelica gigas led to isolation and identification of a new coumarin, peucedanone (12), and isolation of 11 known coumarins. Among them, decursinol (1) represented the highest inhibitory activity toward AChE in vitro. The correlation of the inhibitory activities of the coumarins toward AChE with their chemical structures was studied.

Citing Articles

Angelica gigas Nakai (Korean Dang-gui) Root Alcoholic Extracts in Health Promotion and Disease Therapy - active Phytochemicals and In Vivo Molecular Targets.

Lu J, Jiang C, Drabick J, Joshi M, Perimbeti S Pharm Res. 2025; 42(1):25-47.

PMID: 39779619 PMC: 11785709. DOI: 10.1007/s11095-024-03809-9.


Combining Deep Learning and Structural Modeling to Identify Potential Acetylcholinesterase Inhibitors from .

Sutthibutpong T, Posansee K, Liangruksa M, Termsaithong T, Piyayotai S, Phitsuwan P ACS Omega. 2024; 9(14):16311-16321.

PMID: 38617639 PMC: 11007777. DOI: 10.1021/acsomega.3c10459.


Natural Inhibitors of Cholinesterases: Chemistry, Structure-Activity and Methods of Their Analysis.

Smyrska-Wieleba N, Mroczek T Int J Mol Sci. 2023; 24(3).

PMID: 36769043 PMC: 9916849. DOI: 10.3390/ijms24032722.


Natural products as sources of acetylcholinesterase inhibitors: Synthesis, biological activities, and molecular docking studies of osthole-based ester derivatives.

Yu X, Zhang Y, Zhang M, Chen Y, Yang W Front Plant Sci. 2022; 13:1054650.

PMID: 36466282 PMC: 9716088. DOI: 10.3389/fpls.2022.1054650.


Plant Pyranocoumarins: Description, Biosynthesis, Application.

Khandy M, Sofronova A, Gorpenchenko T, Chirikova N Plants (Basel). 2022; 11(22).

PMID: 36432864 PMC: 9693251. DOI: 10.3390/plants11223135.