2015
DOI: 10.1016/j.phytol.2015.04.018
|View full text |Cite
|
Sign up to set email alerts
|

Two new pentacyclic triterpenoids from the stems of Manihot esculenta

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(3 citation statements)
references
References 23 publications
0
3
0
Order By: Relevance
“…Although there is a lack of research on their mechanism of action, the study proposed that the unsaturation of the chemical structure may significantly contribute to their anti-cancer property. 88…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…Although there is a lack of research on their mechanism of action, the study proposed that the unsaturation of the chemical structure may significantly contribute to their anti-cancer property. 88…”
Section: Discussionmentioning
confidence: 99%
“…Worthy of note that both compounds are cis-trans isomers of each other, which have demonstrated moderate anti-cancer activity where the configuration of the double bond may play a significant role in its cytotoxic activity. 88 Recently, silica gel column was employed to isolate and identify two new terpenoids from ethanolic cassava stem extract, namely sporogen AO-2, a sesquiterpene, and thecacorin C, a diterpene. Both compounds were found to display modest anti-bacterial activity upon examination.…”
Section: Phytochemistrymentioning
confidence: 99%
See 1 more Smart Citation