Abstract
Six previously undescribed components, bis(4-glycosyloxybenzyl) 2-isobutyltartrate derivatives (pholidotoside A-E) and phenolic glycoside (pholidotosin A), together with twenty known compounds were isolated from the pseudobulbs of Pholidota chinensis. Their structures and absolute configuration were elucidated and established through various spectroscopic and chemical methods. The anti-inflammatory potential of selected compounds was examined using a human neutrophil cell model activated by N-formyl-methionyl-leucyl-phenylalanine/cytochalasin B (fMLP/CB). Among these, dihydrophenanthrenes exhibited potent inhibitory effect on both superoxide anion generation and elastase release assays with IC 50 values ranging from 0.41 ± 0.05 to 7.14 ± 0.30 μM.
Original language | American English |
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Article number | 113528 |
Pages (from-to) | 113528 |
Journal | Phytochemistry |
Volume | 206 |
DOIs | |
State | Published - 02 2023 |
Bibliographical note
Copyright © 2022 Elsevier Ltd. All rights reserved.Keywords
- Anti-inflammatory activity
- Dihydrophenanthrenes
- Glycosyloxybenzyl isobutyltartrates
- Orchidaceae
- Pholidota chinensis
- Humans
- Neutrophils
- Phenols/pharmacology
- Anti-Inflammatory Agents/pharmacology
- Superoxides/pharmacology
- Animals
- Pangolins
- N-Formylmethionine Leucyl-Phenylalanine/pharmacology