Meroterpenes and prenylated benzoylphloroglucinol from the flowers of Hypericum formosanum.
Anti-neuroinflammatory activity
Formohyperins
Hypericaceae
Hypericum formosanum
Meroterpene
Journal
Phytochemistry
ISSN: 1873-3700
Titre abrégé: Phytochemistry
Pays: England
ID NLM: 0151434
Informations de publication
Date de publication:
Apr 2024
Apr 2024
Historique:
received:
23
11
2023
revised:
07
02
2024
accepted:
09
02
2024
medline:
18
3
2024
pubmed:
17
2
2024
entrez:
16
2
2024
Statut:
ppublish
Résumé
Formohyperins A-F, previously undescribed meroterpenes, and grandone, a prenylated benzoylphloroglucinol being considered to be one of their biogenetic precursors, were isolated from the flowers of a Hypericaceous plant, Hypericum formosanum Maxim. Detailed spectroscopic analyses showed that formohyperins A-D were meroterpenes with an enolized 3-phenylpropane-1,3-dione moiety. Formohyperins E and F were elucidated as meroterpenes having a 4-benzoyl-5-hydroxycyclopent-4-ene-1,3-dione moiety. Formohyperins A-C and E were optically active, and their absolute configurations were deduced by comparison of the experimental and TDDFT calculated ECD spectra. In contrast, formohyperin D was concluded to be a racemate. Formohyperins A-F and grandone were found to show inhibitory activities against LPS-stimulated IL-1β production from murine microglial cells with EC
Identifiants
pubmed: 38364882
pii: S0031-9422(24)00053-0
doi: 10.1016/j.phytochem.2024.114016
pii:
doi:
Substances chimiques
Phloroglucinol
DHD7FFG6YS
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
114016Informations de copyright
Copyright © 2024 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare no conflict of interest.