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Cycloartane-type triterpenoids from Combretum quadrangulare Kurz with PCSK9 secretion inhibitory activities

Authors
An, Chae-YeongPel, PiseyBae, MingooPark, Chan-WoongKwon, HaeunLee, Hyun SukVan Dung, LuongKim, ChangmuLee, DonghoChoi, Young HeeChin, Young-Won
Issue Date
Feb-2025
Publisher
ELSEVIER
Keywords
Combretum quadrangulare; Combretaceae; Cycloartane; Triterpenoid; VCD; PCSK9; LDL; Hypercholesterolemia
Citation
Phytochemistry, v.230, pp 1 - 17
Pages
17
Indexed
SCIE
SCOPUS
Journal Title
Phytochemistry
Volume
230
Start Page
1
End Page
17
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/57826
DOI
10.1016/j.phytochem.2024.114330
ISSN
0031-9422
1873-3700
Abstract
Nine previously undescribed (1-9) and seven known (10-16) cycloartane-type triterpenoids were isolated and characterized from Combretum quadrangulare Kurz using physicochemical and spectroscopic methods. The absolute configurations of these compounds were determined through modified Mosher's method and quantum chemical calculation of electronic circular dichroism (ECD) and vibrational circular dichroism (VCD) spectra. Their inhibitory activities against PCSK9 secretion were assessed, and a plausible structure-activity relationship was delineated. Compounds 2, 14, and 15 exhibited notable inhibitory effects on PCSK9 mRNA and protein levels, and significant PCSK9 mRNA inhibition was observed when co-treated with atorvastatin. Compound 15 showed the most potent activity, markedly enhancing LDL uptake compared to the negative control. In vivo pharmacokinetic studies confirmed that compound 15 exhibited higher distribution in the liver than plasma, where PCSK9 is predominantly synthesized. These findings emphasize the potential significance of the cycloartane-type triterpenoid scaffold in discovering PCSK9 inhibitors.
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