Chalcones as a Platform for the Development of Novel Antiviral Agents: A Review.

IF 4 3区 医学 Q2 CHEMISTRY, MEDICINAL
Leonardo Dos Santos Corrêa Amorim, Natasha Cristina da Rocha, Kauê Francisco Corrêa de Souza E Souza, Vitor Won-Held Rabelo, Izabel Christina Nunes de Palmer Paixão
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引用次数: 0

Abstract

Introduction: Viruses pose serious threats to public health, with frequent outbreaks of emerging and reemerging viral pathogens. Given the limitations of current antiviral therapies, the search for new control strategies is essential. In this context, chalcones have attracted great attention due to their structural versatility and a wide range of pharmacological activities, including antiviral effects.

Methods: We conducted a literature review examining the antiviral applications of natural and synthetic chalcones validated in experimental assays and reported in articles published up to December 2025 in the PubMed, Web of Science, and Google Scholar databases.

Results: Chalcones have shown antiviral activity against more than 15 viral species, including respiratory viruses and arboviruses, human retroviruses, DNA viruses, and the plant pathogen tobacco mosaic virus.

Discussion: Structural modifications of the chalcone core influence their mechanisms of action, which involve diverse targets such as viral proteases, kinases, polymerases, structural proteins, as well as host cell pathways. Nevertheless, limited selectivity likely remains a major challenge hindering further development of these compounds.

Conclusion: Overall, the structural versatility of chalcones, their broad-spectrum antiviral activity, and their diverse mechanisms of action highlight their strong potential as antiviral agents. Yet, further optimization and in vivo studies are essential to develop more potent and safer chalcone-based drug candidates.

查尔酮作为开发新型抗病毒药物的平台:综述。
病毒对公共卫生构成严重威胁,新出现和再出现的病毒病原体频繁爆发。鉴于目前抗病毒疗法的局限性,寻找新的控制策略至关重要。在这种情况下,查尔酮因其结构的多功能性和广泛的药理活性(包括抗病毒作用)而引起了人们的极大关注。方法:我们进行了一项文献综述,研究了天然和合成查尔酮的抗病毒应用,这些应用在实验分析中得到验证,并在PubMed、Web of Science和谷歌Scholar数据库中截至2025年12月发表的文章中得到报道。结果:查尔酮对呼吸道病毒和虫媒病毒、人类逆转录病毒、DNA病毒、植物病原体烟草花叶病毒等15种以上的病毒均有抗病毒活性。讨论:查尔酮核心的结构修饰影响其作用机制,其涉及多种靶点,如病毒蛋白酶、激酶、聚合酶、结构蛋白以及宿主细胞途径。然而,有限的选择性可能仍然是阻碍这些化合物进一步发展的主要挑战。结论:查尔酮的结构通用性、广谱抗病毒活性和多种作用机制显示了其作为抗病毒药物的巨大潜力。然而,进一步的优化和体内研究对于开发更有效和更安全的查尔酮类候选药物至关重要。
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来源期刊
CiteScore
7.80
自引率
0.00%
发文量
231
审稿时长
6 months
期刊介绍: The aim of Mini-Reviews in Medicinal Chemistry is to publish short reviews on the important recent developments in medicinal chemistry and allied disciplines. Mini-Reviews in Medicinal Chemistry covers all areas of medicinal chemistry including developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, drug targets, and natural product research and structure-activity relationship studies. Mini-Reviews in Medicinal Chemistry is an essential journal for every medicinal and pharmaceutical chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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