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Phenylpropanoid-Conjugated Triterpenoids from the Leaves of Actinidia arguta and Their Inhibitory Activity on alpha-Glucosidase

Authors
Ahn, Jong HoonPark, YoungkiYeon, Sang WonJo, Yang HeeHan, Yoo KyongTurk, AymanRyu, Se HwanHwang, Bang YeonLee, Ki YongLee, Mi Kyeong
Issue Date
22-May-2020
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF NATURAL PRODUCTS, v.83, no.5, pp.1416 - 1423
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF NATURAL PRODUCTS
Volume
83
Number
5
Start Page
1416
End Page
1423
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/55647
DOI
10.1021/acs.jnatprod.9b00643
ISSN
0163-3864
Abstract
Actinidia arguta, commonly called hardy kiwifruit or kiwiberry, has cold-resistant properties and can be cultivated in Asia, including Korea. Seven new triterpenoids (2-4 and 8-11) along with eight known triterpenoids were isolated from the leaves of A. arguta through various chromatographic techniques. The new triterpenoids were defined as actiniargupenes A-C (2-4), actinidic acid derivatives with phenylpropanoid constituent units, dehydroisoactinidic acid (8), and actiniargupenes D-F (9-11), asiatic acid derivatives with phenylpropanoid substituents, on the basis of 1D and 2D NMR and MS data. Among the triterpenoids, those with a phenylpropanoid constituent unit showed inhibitory activity on alpha-glucosidase, which suggested the importance of the phenylpropanoid moiety. Molecular docking analysis demonstrated the interaction between the 4'-OH group of the phenylpropanoid moiety and alpha-glucosidase.
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