Open AccessLignans and Other Compounds From the Roots of Pandanus tonkinensis and Their Lipid Peroxidation Inhibitory Activity
Author(s) -
Dinh Thi Huyen Trang,
Pham Hung Viet,
Duong Hong Anh,
Bùi Hữu Tài,
Quoc Anh Ngo,
Nguyễn Xuân Nhiệm,
Phan Văn Kiệm
Publication year - 2022
Publication title -
natural product communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.221
H-Index - 44
eISSN - 1934-578X
pISSN - 1555-9475
DOI - 10.1177/1934578x221088372
Subject(s) - lipid peroxidation , chemistry , glucoside , trolox , stereochemistry , antioxidant , biochemistry , antioxidant capacity , medicine , alternative medicine , pathology
A new phenylpropane (1) and 9 known (2-10) compounds were isolated from the methanol extract of Pandanus tonkinensis roots. Their chemical structures were determined as (7 S)-2,6-dimethoxyphenyl-7,9-propanediol-1 -O-β-D-glucopyranoside (1), isorhapontigenin (2), pinoresinol-4,4′-di -O-β-D-glucoside (3), isoeucommin A (4), pinoresinol-4′ -O-β-D-glucoside (5), acanthoside B (6), eucommin A (7), urolignoside (8), benzyl O-α-L-arabinopyranosyl-(1→6) -β-D-glucopyranoside (9), and (6 S,9 S)-roseoside (10) by comprehensive analysis of high-resolution electron spray ionization mass spectrum and nuclear magnetic resonance spectral data, as well as by comparison of their spectral data with those reported in the literature. In addition, the stereochemistry of 1 was successfully determined by both theoretical and calculated CD spectra. All the isolates were tested for their lipid peroxidation inhibitory effects by in vitro assay. Compounds 2-7 exhibited significantly lipid peroxidation inhibitory effects with IC 50 values of 21.3 ± 1.7, 61.9 ± 3.9, 57.5 ± 5.5, 10.4 ± 0.7, 28.9 ± 0.3, 54.2 ± 3.5 µM, respectively, compared to that of the positive control, trolox (31.4 ± 2.2 µM).