2021
DOI: 10.1016/j.phytochem.2021.112769
|View full text |Cite
|
Sign up to set email alerts
|

Quassinoids: Phytochemistry and antitumor prospect

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
16
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 21 publications
(16 citation statements)
references
References 143 publications
0
16
0
Order By: Relevance
“…Interestingly, there exists a structure with 20 carbons appearing in the top 10 skeletons of triterpenoids (the eighth; Fig. 2c), which belongs to a series of bitter compounds called quassinoids mainly found in the Simaroubaceae family (Duan et al ., 2021).…”
Section: Resultsmentioning
confidence: 99%
“…Interestingly, there exists a structure with 20 carbons appearing in the top 10 skeletons of triterpenoids (the eighth; Fig. 2c), which belongs to a series of bitter compounds called quassinoids mainly found in the Simaroubaceae family (Duan et al ., 2021).…”
Section: Resultsmentioning
confidence: 99%
“…While the quassinoid terpenes bruceine A ( 3.31 ) and D ( 3.32 ) reported from the Chinese medicinal plant Brucea javanica (Simaroubaceae) ( yadanzi ) were strongly active against the fish flatworm D. intermedius (EC 50 0.49 and 0.57 μg mL −1 , respectively), 68 they were also potent inhibitors of cell proliferation by inducing apoptosis, 69,70 and exhibited antimalarial, anti-inflammatory, antifeedant, insecticidal, amoebicidal, antiulcer and herbicidal activities. 70 It was also recently reported that 3.31 had an apoptosis-like effect on the reproductive tissues of C. elegans .…”
Section: Plantsmentioning
confidence: 99%
“…Within the last few years, several original research papers and in-depth reviews have been published discussing the biological function and structure-activity relationship (SAR) of quassinoids; consequently, this topic is not covered in detail herein. [48][49][50] In general, the α,β-unsaturated ketone in ring A, the C-15 ester side chain, and the tetrahydrofuran bridge are key contributors to bioactivity; however, the mechanism of action of different quassinoids likely diverges considerably, and specific targets have rarely been unambiguously linked to the biological properties observed in phenotypic assays. The lack of mechanistic understanding is clearly one of the main factors currently limiting the therapeutic potential of quassinoids.…”
Section: Selected Structure-activity Relationships and Investigations...mentioning
confidence: 99%