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Inflammation is a fundamental biological reaction to harmful stimuli, which is crucial in the initiation and advancement of different diseases, including rheumatoid arthritis, cardiovascular conditions, neurological disorders such as Alzheimer's and Parkinson's, and multiple cancer types. Chronic inflammation, in particular, contributes to irreversible tissue damage and the progression of disease. Thus, the suppression of key inflammatory mediators has become a promising therapeutic approach. Thromboxane A2 (TxA2), tumor necrosis factor-alpha (TNF-α), and interleukin-6 (IL-6) are among the mediators that have been thoroughly investigated for their roles in regulating immune responses and sustaining inflammation; therefore, targeting these mediators offers substantial therapeutic potential. In recent years, significant attention has been focused on heterocyclic compounds, especially pyridazine and pyridazinone derivatives, owing to their structural diversity and extensive biological activity. These scaffolds have shown significant effectiveness in regulating inflammatory pathways by limiting TxA2 production, reducing TNF-α release, and disrupting IL-6 signaling. This review presents a comprehensive overview of pyridazine and pyridazinone-based compounds as potential anti-inflammatory agents. It highlights both traditional and current synthetic strategies used in their development and explores their mechanisms of action with respect to key inflammatory targets. Additionally, the study examines recent pharmacological assessments and preclinical results, offering insights into the medicinal uses of these substances. A brief perspective on future research directions is also included, emphasizing the need for further structural optimization, in vivo validation, and clinical translation. Collectively, these results highlight the potential of pyridazine and pyridazinone derivatives in the development of advanced anti-inflammatory pharmaceuticals.
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http://dx.doi.org/10.2174/0113895575404189250811070603 | DOI Listing |
Mini Rev Med Chem
August 2025
Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Modern University for Technology and Information (MTI), Cairo 11571, Egypt.
Inflammation is a fundamental biological reaction to harmful stimuli, which is crucial in the initiation and advancement of different diseases, including rheumatoid arthritis, cardiovascular conditions, neurological disorders such as Alzheimer's and Parkinson's, and multiple cancer types. Chronic inflammation, in particular, contributes to irreversible tissue damage and the progression of disease. Thus, the suppression of key inflammatory mediators has become a promising therapeutic approach.
View Article and Find Full Text PDFACS Omega
August 2025
Korea Institute of Ocean Science & Technology (KIOST), Busan 49111, Republic of Korea.
Luffariellolide () was previously isolated in useful quantities (>200 mg) from the marine sponge sp., collected from the Philippines. The intrinsic antibacterial activity of was insignificant; however, 2-(pyridinyl)-pyridazinone , derived from , exhibited considerable activity against .
View Article and Find Full Text PDFEur J Med Chem
October 2025
State Key Laboratory of Esophageal Cancer Prevention and Treatment, Key Laboratory of Advanced Pharmaceutical Technology, Ministry of Education of China, School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, PR China. Electronic address:
Aberrant activity of histone methyltransferase polycomb repressive complex 2 (PRC2) is associated with cancers and other diseases. Recently, compounds that bind to the EED subunit of PRC2 have emerged as allosteric inhibitors of PRC2, suggesting that targeting EED represents a novel strategy for human diseases. In this study, we designed and synthesized a new array of pyridazinone-based EED inhibitors derived from hit 6 identified through virtual screening, which was further optimized via extensive structure-activity relationship (SAR) studies.
View Article and Find Full Text PDFPest Manag Sci
September 2025
Agro & Life Solutions Research Laboratory, Sumitomo Chemical Co., Ltd., Hyogo, Japan.
Background: Acetyl-coenzyme A carboxylase (ACCase) is one of the most important enzymes involved in the biosynthesis of fatty acids in both plants and animals, and its inhibitors are widely used to control gramineous plants or sucking pests in crop fields. Phenyl-substituted cyclic keto-enols (CKEs) are known as a chemical class inhibiting ACCase, and several compounds are commercially available as herbicides or insecticides.
Results: We synthesized a new series of phenyl-substituted CKEs containing a pyridazinone moiety and examined the structure-activity relationship (SAR) based on herbicidal activity.
Int J Mol Sci
April 2025
Department of Medicine, Surgery and Pharmacy, University of Sassari, Via Muroni 23/A, 07100 Sassari, Italy.
Pyridazin-3(2)one-based molecules have always attracted the attention of medicinal chemists due to their different pharmacological properties. The incorporation of such nuclei in therapeutically active molecules either as monocyclic units or as fused bi- or tricyclic scaffolds results in a wide range of pharmacological effects such as anti-inflammatory, analgesic, anticancer, antimicrobial, antiviral, cardiovascular-protective, antiulcer, and many other useful pharmacological activities. In accordance with our consolidated experience gained over the years in the chemistry and biology of tricyclic pyridazin-3(2)ones, this review summarizes SAR studies of such pyridazinone-based polycyclic compounds endowed with various biological and therapeutic properties.
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