Four new cytotoxic triterpenoids from <i>Euphorbia fischeriana</i>

Our ongoing phytochemical investigation on <i>Euphorbia fischeriana</i> led to isolation of four new cytotoxic triterpenoids (<b>1-4</b>), along with twenty three known analogues (<b>5-27</b>). The new structures were characterised as fiseuphanins C-F (<b>1-4</b>) by NMR and HRESIMS spectroscopic experiments. Among them, isolates <b>8-15</b>, <b>17-20</b>, <b>22</b>, and <b>25-27</b> were the first examples from <i>E. fischeriana.</i> Compounds <b>2</b>, <b>11</b>, and <b>13</b> exhibited significant cytotoxic activity against MCF-7 cell line with IC<sub>50</sub> of 0.04, 6.30, and 2.44 µM, respectively, whereas, only compounds <b>6</b>, <b>8</b>, <b>11</b>, and <b>23</b> exhibited weak inhibitory activity against A549 with IC<sub>50</sub> values ranging from 36.37 to 81.49 µM.

Authors

Institutions

Publication Details

Journal
Natural Product Research
Published
2025-05-16
DOI
https://doi.org/10.1080/14786419.2025.2503015
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Four new cytotoxic triterpenoids from Euphorbia fischeriana

Ting-Xiang Shi, Yuan-Biao He, Yong Zhao, Yu-Ping Huang et al.
Natural Product Research
Bioactive Natural Diterpenoids Research
article

Four new cytotoxic triterpenoids from Euphorbia fischeriana

Ting-Xiang Shi, Yuan-Biao He, Yong Zhao, Yu-Ping Huang, Jing Yang, Yanni Ma, Wen-Na Li
article en

Abstract

Our ongoing phytochemical investigation on <i>Euphorbia fischeriana</i> led to isolation of four new cytotoxic triterpenoids (<b>1-4</b>), along with twenty three known analogues (<b>5-27</b>). The new structures were characterised as fiseuphanins C-F (<b>1-4</b>) by NMR and HRESIMS spectroscopic experiments. Among them, isolates <b>8-15</b>, <b>17-20</b>, <b>22</b>, and <b>25-27</b> were the first examples from <i>E. fischeriana.</i> Compounds <b>2</b>, <b>11</b>, and <b>13</b> exhibited significant cytotoxic activity against MCF-7 cell line with IC<sub>50</sub> of 0.04, 6.30, and 2.44 µM, respectively, whereas, only compounds <b>6</b>, <b>8</b>, <b>11</b>, and <b>23</b> exhibited weak inhibitory activity against A549 with IC<sub>50</sub> values ranging from 36.37 to 81.49 µM.

Natural Product Research
Yunnan Normal University (CN), Kunming Institute of Botany (CN), Chinese Academy of Sciences (CN), Kunming Municipal Hospital of Traditional Chinese Medicine (CN), Yunnan University of Traditional Chinese Medicine (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 90%
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.