Bioactive Coumarins: Bioorganic Strategies for Targeting Enzymes, Receptors, and DNA

IF 1.7 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yasser Fakri Mustafa
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引用次数: 0

Abstract

Coumarins, a structurally diverse class of naturally occurring and synthetic compounds, have emerged as pivotal entities in modern bioorganic chemistry. Centered around the 2H-1-benzopyran-2-one scaffold, these molecules exhibit remarkable structural plasticity, enabling fine-tuned interactions with a broad spectrum of biological targets, including enzymes, nucleic acids, and cellular receptors. This review provides a detailed overview of bioactive coumarins and their growing importance as molecular modulators and scaffolds in drug discovery and design. Special emphasis is placed on their dual role as both therapeutic agents and diagnostic probes, capable of engaging in covalent and non-covalent interactions within biological systems. The discussion highlights how strategic structural modifications enhance coumarins’ specificity and potency toward key biological macromolecules. Mechanistic insights into coumarin-based enzyme inhibition are explored, particularly with respect to active and allosteric site binding, using representative examples involving dehydrogenases, DNA repair enzymes, and cytoskeletal proteins. Furthermore, the review delves into the interaction of coumarins with nuclear receptors, such as estrogen, glucocorticoid, and peroxisome proliferator-activated receptors, elucidating their roles in modulating neurological, cardiovascular, and immunological functions. Special attention is given to the nucleic acid-binding potential of coumarins, particularly their involvement in DNA intercalation and G-quadruplex stabilization, which are promising strategies in anticancer therapy. The review also examines recent advances in sustainable synthetic methodologies, including microwave-assisted and green chemistry approaches. Analytical tools like fluorescence spectroscopy and chromatographic techniques are emphasized for their critical role in evaluating structure–activity relationships and biological responses. Finally, the pharmacokinetic behavior, safety considerations, and emerging nanotechnology-enabled delivery systems are discussed. In vivo and clinical findings underscore the translational relevance of coumarins, particularly in oncology, infectious diseases, and neurodegenerative conditions. Looking ahead, coumarins stand out as versatile molecular platforms with immense potential to inspire innovative therapeutic strategies through interdisciplinary collaboration.

Abstract Image

生物活性香豆素:针对酶、受体和DNA的生物有机策略
香豆素是一类结构多样的天然和合成化合物,在现代生物有机化学中已成为关键的实体。这些分子以2h -1-苯并吡喃-2- 1支架为中心,表现出显著的结构可塑性,能够与广泛的生物靶标(包括酶、核酸和细胞受体)进行微调的相互作用。本文详细介绍了生物活性香豆素及其在药物发现和设计中作为分子调节剂和支架的重要性。特别强调的是它们作为治疗剂和诊断探针的双重作用,能够参与生物系统内的共价和非共价相互作用。讨论强调了战略性结构修饰如何增强香豆素对关键生物大分子的特异性和效力。利用脱氢酶、DNA修复酶和细胞骨架蛋白等代表性例子,探讨了以香豆素为基础的酶抑制机制,特别是活性和变构位点结合。此外,本文还深入探讨了香豆素与核受体(如雌激素、糖皮质激素和过氧化物酶体增殖激活受体)的相互作用,阐明了它们在调节神经、心血管和免疫功能中的作用。特别关注的是香豆素的核酸结合潜力,特别是它们参与DNA嵌入和g -四联体稳定,这是抗癌治疗中有前途的策略。本报告还审查了可持续合成方法的最新进展,包括微波辅助和绿色化学方法。分析工具,如荧光光谱和色谱技术强调其在评估结构-活性关系和生物反应的关键作用。最后,讨论了药代动力学行为、安全性考虑和新兴的纳米技术支持的给药系统。体内和临床研究结果强调了香豆素的翻译相关性,特别是在肿瘤、传染病和神经退行性疾病方面。展望未来,香豆素作为多功能分子平台脱颖而出,具有巨大的潜力,通过跨学科合作激发创新的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Russian Journal of Bioorganic Chemistry
Russian Journal of Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
1.80
自引率
10.00%
发文量
118
审稿时长
3 months
期刊介绍: Russian Journal of Bioorganic Chemistry publishes reviews and original experimental and theoretical studies on the structure, function, structure–activity relationships, and synthesis of biopolymers, such as proteins, nucleic acids, polysaccharides, mixed biopolymers, and their complexes, and low-molecular-weight biologically active compounds (peptides, sugars, lipids, antibiotics, etc.). The journal also covers selected aspects of neuro- and immunochemistry, biotechnology, and ecology.
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