Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds.

Advanced glycation endproducts Antidesma bunius Coumarinolignan Cyclopeptide Euphorbiaceae

Journal

Phytochemistry
ISSN: 1873-3700
Titre abrégé: Phytochemistry
Pays: England
ID NLM: 0151434

Informations de publication

Date de publication:
Oct 2022
Historique:
received: 08 03 2022
revised: 21 06 2022
accepted: 27 06 2022
pubmed: 8 7 2022
medline: 8 9 2022
entrez: 7 7 2022
Statut: ppublish

Résumé

Thirty-three natural products were isolated from the aerial parts of Antidesma bunius, Euphorbiaceae, a plant used in Vietnamese traditional medicine against rheumatoid arthritis. All compounds were reported the first time for this species, and nine constituents resembled undescribed natural products, noticeably three coumarinolignans with 2,2-dimethyl-1,3-dioxolane moiety, two cyclopeptides, and two furofuran-type lignans connected with a phenylpropanoid moiety. The individual structures were elucidated by combining NMR and MS data, and their configuration was established by NOESY and ECD experiments and NMR calculations. Compounds with sufficient amount were analyzed for their inhibition of advanced glycation endproducts (AGEs) formation, metabolites involved in many diseases like Alzheimer, joint diseases or diabetes. With IC

Identifiants

pubmed: 35798090
pii: S0031-9422(22)00216-3
doi: 10.1016/j.phytochem.2022.113300
pii:
doi:

Substances chimiques

Biological Products 0
Glycation End Products, Advanced 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113300

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Hieu Nguyen-Ngoc (H)

Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI), University of Innsbruck, Innrain 80-82/IV, 6020, Innsbruck, Austria; Faculty of Pharmacy, PHENIKAA University, Hanoi, 12116, Viet Nam.

Mostafa Alilou (M)

Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI), University of Innsbruck, Innrain 80-82/IV, 6020, Innsbruck, Austria.

Séverine Derbré (S)

SONAS, EA921, UNIV Angers, SFR QUASAV, Faculty of Health Sciences, Dpt Pharmacy, 16 Bd Daviers, 49045, Angers cedex 01, France.

Patricia Blanchard (P)

SONAS, EA921, UNIV Angers, SFR QUASAV, Faculty of Health Sciences, Dpt Pharmacy, 16 Bd Daviers, 49045, Angers cedex 01, France.

Giang Nam Pham (GN)

College of Pharmacy, Chungnam National University, Daejeon, 34134, Republic of Korea.

Duc Trong Nghiem (DT)

Department of Botany, Hanoi University of Pharmacy, 13-15 Le Thanh Tong, Hoan Kiem, Hanoi, 10000, Viet Nam.

Pascal Richomme (P)

SONAS, EA921, UNIV Angers, SFR QUASAV, Faculty of Health Sciences, Dpt Pharmacy, 16 Bd Daviers, 49045, Angers cedex 01, France.

Hermann Stuppner (H)

Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI), University of Innsbruck, Innrain 80-82/IV, 6020, Innsbruck, Austria.

Markus Ganzera (M)

Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI), University of Innsbruck, Innrain 80-82/IV, 6020, Innsbruck, Austria. Electronic address: markus.ganzera@uibk.ac.at.

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Classifications MeSH