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Forward Pharmaceutical Science | Publishing Language: Chinese | Open Access

Research progress of Plasmodium falciparum histone deacetylase inhibitors

Center for Drug Evaluation, National Medical Products Administration, Beijing 102600
Artemisinin Research Center, China Academy of Chinese Medical Science, Beijing 100700, China
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Abstract

Histone deacetylase has proved to be a promising new antimalarial target in the development of novel antimalarial drugs. This article introduces the mechanism of action of histone deacetylase inhibitors and their antimalarial activity, with a focus on the discovery process of Plasmodium histone deacetylase inhibitors and their recent research progress both domestically and internationally. Recent research findings on hydroxamic acid-based and cyclic peptide inhibitors are reviewed and analyzed in detail according to their different structural types. Key challenges hindering drug development and approval, such as drug toxicity issues and the lag in related biological studies, are highlighted. Furthermore, future directions for drug research and development are proposed, offering insights for the further development of new antimalarial drugs.

CLC number: R914.2;R963 Document code: A Article ID: 1000-5048(2026)-1-28-6

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Journal of China Pharmaceutical University
Pages 28-33

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Cite this article:
ZHAO L, ZHANG M, SUN P. Research progress of Plasmodium falciparum histone deacetylase inhibitors. Journal of China Pharmaceutical University, 2026, 57(1): 28-33. https://doi.org/10.11665/j.issn.1000-5048.2025031901

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Received: 19 March 2025
Published: 25 February 2026
© 2026 The Editorial Office of Journal of China Pharmaceutical University

This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/).