Diterpenoid and triterpenoid derivatives from <i>Euphorbia kansui</i> and their anti-inflammatory activity

Thirteen ingenane-type (1–13), four jatrophane-type (14–17), and one nor-abietane-type diterpenoids (18), together with three tirucallane-type (19–21), two lanostane-type (22 and 23), and one lupane-type triterpenoids (24), were isolated from the roots of Euphorbia kansui. Among them, compound 19, named sclerodol C, was a new compound. Their structures were determined by analysis of HRESIMS and NMR spectral data. Compounds 1, 3, 5, 6, 8, 10, 19, 20, 21, and 22 exhibited significant NO inhibitory activity in LPS-induced RAW 264.7 cells. Furthermore, molecular docking indicated that compounds 19 and 22 had a favourable binding affinity for NLRP3, iNOS, Akt, and NF-κB.

Authors

Institutions

Publication Details

Journal
Natural Product Research
Published
2026-06-25
DOI
https://doi.org/10.1080/14786419.2026.2692568
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Diterpenoid and triterpenoid derivatives from Euphorbia kansui and their anti-inflammatory activity

Yue-Tong Zhu, Xi Zhang, Lu Xie, Bo Wei et al.
Natural Product Research
Bioactive Natural Diterpenoids Research
article

Diterpenoid and triterpenoid derivatives from Euphorbia kansui and their anti-inflammatory activity

Yue-Tong Zhu, Xi Zhang, Lu Xie, Bo Wei, Jin-Ming Gao, Shu-Han Yang
article en

Abstract

Thirteen ingenane-type (1–13), four jatrophane-type (14–17), and one nor-abietane-type diterpenoids (18), together with three tirucallane-type (19–21), two lanostane-type (22 and 23), and one lupane-type triterpenoids (24), were isolated from the roots of Euphorbia kansui. Among them, compound 19, named sclerodol C, was a new compound. Their structures were determined by analysis of HRESIMS and NMR spectral data. Compounds 1, 3, 5, 6, 8, 10, 19, 20, 21, and 22 exhibited significant NO inhibitory activity in LPS-induced RAW 264.7 cells. Furthermore, molecular docking indicated that compounds 19 and 22 had a favourable binding affinity for NLRP3, iNOS, Akt, and NF-κB.

Natural Product Research
Kangmei Pharmaceutical (China) (CN), Buchang Pharma (China) (CN), Northwest A&F University (CN)
Zero hunger
Openalex Percentile: Top 11%
Bioactive Natural Diterpenoids Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.