Recent advances of piperine and its derivatives as potential anticancer agents

Abstract

Piperine, a crucial ingredient of the plant Piper nigrum, exhibits a broad spectrum of biological activities and has attracted interest as a potential anticancer agent. With a low yield in natural resources, chemists have developed several synthetic methods for piperine. In addition, low water solubility and poor bioavailability of piperine have significantly limited its therapeutic application. Structural modification, particularly at its piperidine moiety, enables the introduction of diverse functional groups to afford piperine derivatives with improved anticancer potency and favorable pharmacodynamic profiles. This article reviews the recent advances (from 2012 to 2025) in the structural characterization, chemical synthesis, biosynthesis, anticancer profile, structural modification, and structure activity relationship of piperine, which may provide useful direction for the development of more effective piperine-based anticancer candidates or agents.

Article information

Article type
Review Article
Submitted
20 Mar 2026
Accepted
20 May 2026
First published
21 May 2026
This article is Open Access
Creative Commons BY-NC license

RSC Med. Chem., 2026, Accepted Manuscript

Recent advances of piperine and its derivatives as potential anticancer agents

Q. Yu, Z. Liu, J. Liu and L. Bai, RSC Med. Chem., 2026, Accepted Manuscript , DOI: 10.1039/D6MD00223D

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements