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Review | Publishing Language: Chinese | Open Access

Research progress of the multi-target anti-inflammatory drugs based on the arachidonic acid pathway

Gansu University of Chinese Medicine, Lanzhou 730000
Department of Laboratory Medicine, The First Hospital of Lanzhou University, Lanzhou 730000
Key Laboratory of Chemistry and Quality for Traditional Chinese Medicine(TCM)of Colleges of Gansu Province, Lanzhou 730000
Gansu Provincial Engineering Laboratory for TCM Standardization Technology and Popularization, Lanzhou 730000
Lanzhou Institute for Food and Drug Control, Lanzhou 730000, China
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Abstract

Arachidonic acid can be transformed into a variety of metabolites that trigger an inflammatory response through cyclooxygenase, lipoxygenase, cytochrome P450 enzymes, and other metabolic pathways. Moreover, it plays a key role in the occurrence and development of inflammatory diseases. In recent years, multi-target drugs based on the arachidonic acid metabolic pathway have become an important direction of anti-inflammatory drug research. This article summarizes the opportunities and challenges of arachidonic acid metabolic pathways as well as their interference in the development of anti-inflammatory drugs, reviews the research progress of multi-target drug design, synthesis, and anti-inflammatory activity based on the arachidonic acid metabolic pathway, and discusses the difficulties and prospects of multi-target drugs based on metabolic pathways in anti-inflammatory drug development, aiming to provide some reference and inspiration for the study of multi-target anti-inflammatory drugs based on the arachidonic acid metabolic pathway.

CLC number: R96 Document code: A Article ID: 1000-5048(2025)06-0782-11

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Journal of China Pharmaceutical University
Pages 782-792

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Cite this article:
WU D, CUI L, XU F, et al. Research progress of the multi-target anti-inflammatory drugs based on the arachidonic acid pathway. Journal of China Pharmaceutical University, 2025, 56(6): 782-792. https://doi.org/10.11665/j.issn.1000-5048.2024122703

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Received: 27 December 2024
Published: 25 December 2025
© 2025 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/).