LC/MS guided discovery of new kavalactone derivatives in the pericarps of Alpinia zerumbet.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: LC/MS guided discovery of new kavalactone derivatives in the pericarps of Alpinia zerumbet.
Συγγραφείς: Nishidono Y; Pharmaceutical Research and Technology Institute, Kindai University, Higashi-osaka, Osaka 577-8502, Japan; College of Pharmaceutical Sciences, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan. Electronic address: nisidono@phar.kindai.ac.jp., Okuyama T; Department of Pancreatobiliary Surgery, Kansai Medical University, Hirakata, Osaka 573-1010, Japan., Nakatake R; Department of Pancreatobiliary Surgery, Kansai Medical University, Hirakata, Osaka 573-1010, Japan., Tanaka K; College of Pharmaceutical Sciences, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan., Morikawa T; Pharmaceutical Research and Technology Institute, Kindai University, Higashi-osaka, Osaka 577-8502, Japan; Antiaging Center, Kindai University, Higashi-osaka, Osaka 577-8502, Japan.
Πηγή: Fitoterapia [Fitoterapia] 2026 Oct; Vol. 194, pp. 107450. Date of Electronic Publication: 2026 Sep 04.
Τύπος έκδοσης: Journal Article
Γλώσσα: English
Στοιχεία περιοδικού: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 16930290R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-6971 (Electronic) Linking ISSN: 0367326X NLM ISO Abbreviation: Fitoterapia Subsets: MEDLINE
Imprint Name(s): Publication: 1999- : [Amsterdam] : Elsevier
Original Publication: Milano : Inverni & Della Beffa S.p.A.
Ιατρικοί όροι (MeSH): Alpinia*/chemistry , Pyrones*/chemistry , Pyrones*/isolation & purification , Lactones*/chemistry , Lactones*/isolation & purification, Fruit/chemistry ; Chromatography, Liquid/methods ; Monoterpenes/chemistry ; Monoterpenes/isolation & purification ; Plant Extracts/chemistry ; Magnetic Resonance Spectroscopy ; Mass Spectrometry
Περίληψη: An LC/MS guided phytochemical investigation of the pericarps of Alpinia zerumbet yielded five new kavalactone derivatives (1, 4, 5, 21, and 22) along with some known compounds. These comprised two new kavalactone-monoterpene conjugates possessing tricyclic α-pyrone or bicyclic α-pyrone scaffolds and three new hydroxylated kavalactones. Their structures were elucidated by comprehensive spectroscopic analyses (HRESIMS and 1D/2D NMR) and TD-DFT ECD calculations. Moreover, the absolute configuration of the previously described zerumin E4 (18) was revised. Plausible biosynthetic pathways are proposed to rationalize the oxidative derivatization of kavalactone scaffolds and the limited diastereomeric outcomes observed in the kavalactone-monoterpene conjugates. The present findings expand the current knowledge of chemical diversity of the pericarps and provide insights into the phytochemical basis underlying the medicinal use of A. zerumbet fruits.
(Copyright © 2026 Elsevier B.V. All rights reserved.)
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Contributed Indexing: Keywords: Alpinia zerumbet; Kavalactone derivatives; Shell ginger; Zingiberaceae; α-Pyrones
Substance Nomenclature: 0 (Pyrones)
0 (Lactones)
0 (Monoterpenes)
0 (Plant Extracts)
Entry Date(s): Date Created: 20260828 Date Completed: 20260928 Latest Revision: 20260928
Update Code: 20260929
DOI: 10.1016/j.fitote.2026.107450
PMID: 42665056
Βάση Δεδομένων: MEDLINE