Chemical Constituents From <i>Pseudocaryopteris foetida</i>

One undescribed iridoid glucoside, (1S,5R,6R,8S,9S,7''S)-6'-O-3-(4-hydroxyphenyl)-3-methoxypropionyl phlorigidoside B (1); one new diterpenoid glycoside, (3S,5R,7R,10S,15S)-7α-methoxy-12-O-β-D-glucopyranosyl-3,11,16-trihydroxyabieta-8,11,13-triene (2); and one new flavonoid glycoside pectolinarigenin 7-O-(β-D-apiofuranosyl)-(1→6)-β-D-glucopyranoside (3), along with 21 known compounds (4-24), were isolated from the ethyl acetate fraction of Pseudocaryopteris foetida (D. Don) P.D. Cantino. Their structures were elucidated using one- and two-dimensional NMR and high-resolution electrospray ionization mass spectroscopy. Compounds 1, 2, 7-12, 16, 17, 20, 23, and 24 exhibited moderate anti-inflammatory activity via the inhibition of NO production in LPS-induced RAW 264.7 cells.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2026-03-31
DOI
https://doi.org/10.1002/cbdv.71152
Primary Topic
Phytochemistry and Biological Activities
Type
article
Field-Weighted Citation Impact
0.00

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article

Chemical Constituents From Pseudocaryopteris foetida

T. J. Chen, Ping‐Ling Liu, Gui‐Xin Chou, Yong‐Li Wang et al.
Chemistry & Biodiversity
Phytochemistry and Biological Activities
article

Chemical Constituents From Pseudocaryopteris foetida

T. J. Chen, Ping‐Ling Liu, Gui‐Xin Chou, Yong‐Li Wang, Hong‐Tao Xu
article en

Abstract

One undescribed iridoid glucoside, (1S,5R,6R,8S,9S,7''S)-6'-O-3-(4-hydroxyphenyl)-3-methoxypropionyl phlorigidoside B (1); one new diterpenoid glycoside, (3S,5R,7R,10S,15S)-7α-methoxy-12-O-β-D-glucopyranosyl-3,11,16-trihydroxyabieta-8,11,13-triene (2); and one new flavonoid glycoside pectolinarigenin 7-O-(β-D-apiofuranosyl)-(1→6)-β-D-glucopyranoside (3), along with 21 known compounds (4-24), were isolated from the ethyl acetate fraction of Pseudocaryopteris foetida (D. Don) P.D. Cantino. Their structures were elucidated using one- and two-dimensional NMR and high-resolution electrospray ionization mass spectroscopy. Compounds 1, 2, 7-12, 16, 17, 20, 23, and 24 exhibited moderate anti-inflammatory activity via the inhibition of NO production in LPS-induced RAW 264.7 cells.

Chemistry & BiodiversityVol. 23(4)
Shanghai University (CN), Shanghai Innovative Research Center of Traditional Chinese Medicine (CN), Shanghai University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 28%
Phytochemistry and Biological Activities
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