| Literature DB >> 20234973 |
Hai-Tao Xiao1, Jiao Peng, Yan Liang, Jie Yang, Xue Bai, Xiao-Yan Hao, Fu-Mei Yang, Qian-Yun Sun.
Abstract
In a bioassay-guided search for acetylcholinesterase (AChE) inhibitors from Chinese natural resources, eight isoquinoline alkaloids, tetrahydropalmatine (1), corydaline (2), protopine (3), berberine (4), palmatine (5), jatrorrhizine (6), coptisine (7) and dehydrocorydaline (8), were isolated from the methanolic extract of the tubers of Corydalis yanhusuo. Structures of these compounds were identified by spectroscopic techniques. Compounds 4-8 inhibited AChE activity in a dose-dependent manner, and the IC₅₀ values were 0.47 ± 0.01, 0.74 ± 0.06, 2.08 ± 0.09, 1.01 ± 0.03 and 0.62 ± 0.05 µM, respectively. Structure-activity relationship analysis suggested that aromatisation at ring C, as well as substitutions at C-2, C-3, C-9, C-10 and C-13 affect the AChE activity of protoberberine alkaloids.Entities:
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Year: 2011 PMID: 20234973 DOI: 10.1080/14786410802496911
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861