Alkaloids with Acetylcholinesterase Inhibitory Activities from Crinum latifolium L.

A new crinane-type alkaloid, 6-epihydroxypowelline (1), together with six known alkaloids, lycorine (2), 2-O-acetyllycorine (3), deacetylbowdensine (4), 1-epideacetylbowdensine (5), 8-demethyl-3-oxomaritidine (6), and (-)-marithamine (7) were isolated from the whole parts of the Crinum latifolium L. in Vietnam. The structure identification of all compounds was determined by 1D, 2D-NMR as well as HR-ESI-MS spectroscopic techniques. The absolute configuration of these compounds was established by the ECD data. In addition, in vitro inhibition of acetylcholinesterase (AChE) activities was assessed for all isolated alkaloids. All alkaloids had AChE inhibitory effects, with IC<sub>50</sub> values ranging from 32.65 ± 2.72 to 212.76 ± 8.30 µM and compound 3 displayed the strongest inhibition of AChE, with IC<sub>50 </sub>values of 32.65 ± 2.72 µM (in comparison to the reference drug, galanthamine, which had an IC50 of 2.40 ± 0.45 µM).

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Publication Details

Journal
Natural Product Sciences
Published
2024-12-31
DOI
https://doi.org/10.20307/nps.2024.30.4.304
Citations
2
Primary Topic
Chemical synthesis and alkaloids
Type
article
Field-Weighted Citation Impact
0.50
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article

Alkaloids with Acetylcholinesterase Inhibitory Activities from Crinum latifolium L.

Hoang Dac Thang, Do Thanh Tuan, Ngo Viet Duc, Van Cong Pham et al.
2 citations
Natural Product Sciences
Chemical synthesis and alkaloids
0.50
article

Alkaloids with Acetylcholinesterase Inhibitory Activities from Crinum latifolium L.

Hoang Dac Thang, Do Thanh Tuan, Ngo Viet Duc, Van Cong Pham, Đàn Nguyễn Văn, Anh Tuấn Lê, Vu Thi Trang, Hoang Le Tuan Anh, Thắng Nguyễn Thị
article en
2 citations

Abstract

A new crinane-type alkaloid, 6-epihydroxypowelline (1), together with six known alkaloids, lycorine (2), 2-O-acetyllycorine (3), deacetylbowdensine (4), 1-epideacetylbowdensine (5), 8-demethyl-3-oxomaritidine (6), and (-)-marithamine (7) were isolated from the whole parts of the Crinum latifolium L. in Vietnam. The structure identification of all compounds was determined by 1D, 2D-NMR as well as HR-ESI-MS spectroscopic techniques. The absolute configuration of these compounds was established by the ECD data. In addition, in vitro inhibition of acetylcholinesterase (AChE) activities was assessed for all isolated alkaloids. All alkaloids had AChE inhibitory effects, with IC<sub>50</sub> values ranging from 32.65 ± 2.72 to 212.76 ± 8.30 µM and compound 3 displayed the strongest inhibition of AChE, with IC<sub>50 </sub>values of 32.65 ± 2.72 µM (in comparison to the reference drug, galanthamine, which had an IC50 of 2.40 ± 0.45 µM).

Natural Product SciencesVol. 30(4)
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Chemical synthesis and alkaloids
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