Flavonoids and phenylethanoids from the flowers and leaves of Aeschynanthus species and cultivars (Gesneriaceae).


Journal

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

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 13 04 2022
revised: 01 08 2022
accepted: 02 08 2022
pubmed: 25 8 2022
medline: 12 10 2022
entrez: 24 8 2022
Statut: ppublish

Résumé

Forty-one flavones, each one of flavonol, chalcone and dihydroflavonol, two flavanones, and four phenylethanoids were isolated from corollas, calyces and leaves of two Aeschynanthus species, A. fulgens and A. pulcher, and six cultivars, 'Mahligai', 'Mona Lisa', SoeKa', 'Redona', 'Freshya' and 'Bravera'. Flavonoids were mainly the glucuronides and/or methylglucuronides based on hispidulin, nepetin, pectolinarigenin, 6-hydroxyluteolin, scutellarein, apigenin and luteolin, and identified by UV spectra, HR-MS, LC-MS, acid hydrolysis, NMR, and/or HPLC and TLC comparisons with authentic samples. Of these flavonoids, twelve, i.e. hispidulin 7,4'-di-O-glucuronide, 7,4'-di-O-methylglucuronide, 7-O-methylglucuronide-4'-O-glucuronide, 7-O-glucuronide-4'-O-methylglucuronide, 7-O-glucosyl-(1 → 2)-glucuronide and 8-C-glucoside, nepetin 7,4'-di-O-glucuronide, 7-O-glucuronide-4'-O-methylglucuronide and 7-O-methylglucuronide-4'-O-glucuronide, pectolinarigenin 7-O-glucosyl-(1 → 2)-glucuronide and 7-O-xylosyl-(1 → 2)-(6″-malonylglucoside), and 6-hydroxyluteolin 7,4'-di-O-glucuronide, were previously undescribed.

Identifiants

pubmed: 36002075
pii: S0031-9422(22)00283-7
doi: 10.1016/j.phytochem.2022.113367
pii:
doi:

Substances chimiques

Chalcones 0
Flavanones 0
Flavones 0
Flavonoids 0
Flavonols 0
Glucosides 0
Glucuronides 0
Apigenin 7V515PI7F6
Luteolin KUX1ZNC9J2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113367

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Tsukasa Iwashina (T)

Department of Botany, National Museum of Nature and Science, Amakubo 4-1-1, Tsukuba, Ibaraki, 305-0005, Japan. Electronic address: iwashina@kahaku.go.jp.

Sri Rahayu (S)

Bogor Botanic Gardens, Research Center for Plant Conservation and Botanic Gardens, National Agency for Research and Innovation, JI, Ir. H. Juanda 13, Bogor, 26003, West Java, Indonesia.

Takahisa Nakane (T)

Showa Pharmaceutical University, Higashi-tamagawa Gakuen 3-3165, Machida, Tokyo, 194-8543, Japan.

Hari Prasad Devkota (HP)

Graduate School of Pharmaceutical Sciences, Kumamoto University, Oe-honmachi 5-1, Kumamoto, 862-0973, Japan.

Takayuki Mizuno (T)

Department of Botany, National Museum of Nature and Science, Amakubo 4-1-1, Tsukuba, Ibaraki, 305-0005, Japan.

Chie Tsutsumi (C)

Department of Botany, National Museum of Nature and Science, Amakubo 4-1-1, Tsukuba, Ibaraki, 305-0005, Japan.

Didik Widyatmoko (D)

Bogor Botanic Gardens, Research Center for Plant Conservation and Botanic Gardens, National Agency for Research and Innovation, JI, Ir. H. Juanda 13, Bogor, 26003, West Java, Indonesia.

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Classifications MeSH