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Cinnamic acid derivatives as anticancer agents-a review
P De1, M Baltas, F Bedos-Belval
1Université de Toulouse, UPS, LSPCMIB, (Laboratoire de Synthèse et Physico-Chimie de Molécules d'Intérêt Biologique), 118, Route de Narbonne, F-31062 Toulouse Cedex 9, France.
Cinnamic acid derivatives, natural compounds with anticancer potential, are increasingly explored for their antitumor efficacy. This review compiles their synthesis and biological evaluation in anticancer research.
Area of Science:
- Medicinal Chemistry
- Natural Products Chemistry
Background:
- Cinnamic acid and its phenolic analogues are natural compounds with diverse chemical reactivity.
- These compounds have a long history in medicinal research, with early clinical use noted in 1905.
- Despite their potential, cinnamic acid derivatives' anticancer applications have been historically underutilized.
Purpose of the Study:
- To provide a comprehensive literature review on the synthesis and biological evaluation of cinnamic acid derivatives.
- To highlight the recent surge in research interest regarding the antitumor efficacy of cinnamoyl derivatives.
- To consolidate information on various cinnamoyl derivatives, including acids, esters, amides, and hydrazides, for anticancer research.
Main Methods:
- Literature compilation and review.
- Analysis of synthetic routes for cinnamic acid derivatives.
- Evaluation of biological data on anticancer activities.
Main Results:
- Cinnamic acid derivatives possess multiple reactive sites, enabling diverse chemical modifications.
- Significant research attention has focused on cinnamoyl derivatives and their antitumor effects in the last two decades.
- The review compiles extensive data on the synthesis and anticancer evaluation of a wide range of derivatives.
Conclusions:
- Cinnamic acid derivatives represent a promising class of compounds for anticancer drug development.
- This review offers a timely and valuable resource for researchers in medicinal chemistry and oncology.
- Further exploration of these derivatives is warranted to fully realize their therapeutic potential.
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