Paeoniflorin and paeonol from Paeonia species are promising compounds with anticancer and other pharmacological properties

2Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

In this short review, information on the anticancer properties of paeoniflorin (PF) and paeonol (PN) from Paeonia species is collated with reference to the types of cancer, cell lines, effects, and molecular processes. The chemistry, botany, and uses of Paeonia lactiflora and P. suffruticosa, where respective PF and PN are often isolated, are briefly described. PF is a monoterpene glucoside while PN is a phenolic compound. The chemical structure of PF consists of a glucose moiety, a benzoyl moiety, and a cage-like pinane skeleton. PN has a ketone carbonyl side chain at C1, an OH group at C2, and a methoxy component at C4. PF has effects on eight types of cancer cells of which glioma cells are most affected. Liver cancer cells are most affected by PN. In this overview, the anticancer properties of PF and PN against five types of cancer cells are described. Information entails cancer cell types, cancer cell lines, effects, and molecular mechanisms. Some further studies on the anticancer properties of PF and PN are suggested.

Cite

CITATION STYLE

APA

Chan, E. W. C. (2025). Paeoniflorin and paeonol from Paeonia species are promising compounds with anticancer and other pharmacological properties. Journal of Applied Pharmaceutical Science, 15(6), 1–9. https://doi.org/10.7324/JAPS.2025.231323

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free