Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13325
Title: Anti-inflammatory, anti-bacterial and anti-acetylcholinesterase activities of two isoquinoline alkaloids-scoulerine and cheilanthifoline
Authors: Wangchuk P.
Sastraruji T.
Taweechotipatr M.
Keller P.A.
Pyne S.G.
Keywords: amoxicillin
amphotericin B
cheilanthifoline
dexamethasone
galantamine
isoquinoline alkaloid
scoulerine
tumor necrosis factor
unclassified drug
vancomycin
acetylcholinesterase activity
antibacterial activity
antiinflammatory activity
Article
bacterial strain
controlled study
drug activity
drug structure
Helicobacter pylori
minimum inhibitory concentration
nonhuman
Issue Date: 2016
Abstract: Corydalis plants containing isoquinoline alkaloids are reported to possess promising pharmacological properties for the treatment of important diseases including cancer, inflammation, Alzheimer's disease and microbial infections. As part of a wider program investigating Bhutanese medicinal plants, we have previously identified eight isoquinoline alkaloids from C. dubia. Out of these, we report here on two of the major alkaloids, scoulerine (1) and cheilanthifoline (2) and their inhibitory activities against acetylcholinesterase (anti-AChE), tumor necrosis factor alpha (anti TNF-α) and a bacterial strain, Helicobacter pylori. Both alkaloids showed weak anti TNF-α and antibacterial activities. However, the anti-AChE activity of scoulerine (1) was promising as it significantly inhibited AChE with a minimum inhibitory requirement (MIR) value of 0.0015 nmol, which was two-fold better than the reference drug, galanthamine (MIR value of 0.003 nmol). As there are limited anti-Alzheimer's chemotherapeutics, scoulerine (1) is worthy of further exploration, including lead optimization, structure-activity-relationship studies, analog development, pharmacodynamics and in vivo animal studies.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13325
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019168794&doi=10.1177%2f1934578x1601101207&partnerID=40&md5=9a129a1dbef5f0e66ba8d0e090666665
ISSN: 1934578X
Appears in Collections:Scopus 1983-2021

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