Bishnoi Poonam, Saroha Bhavna, Kumar Suresh, Kumar Gourav, Bhardwaj Arpana, Kumari Meena, Kumar Naveen
Department of Chemistry, Kurukshetra University, Kurukshetra, Haryana, India, 136119.
Department of Chemistry, Deenbandhu Chhotu Ram University of Science and Technology, Murthal, Sonipat, India.
Mol Divers. 2025 Feb 7. doi: 10.1007/s11030-025-11110-z.
Recently, it has been seen that there is a rapid surge in Click Chemistry (CC) research owing to its fast, reliable, and biocompatible nature, making it an ideal tool for drug discovery. CC approach allows facile and sustainable development of complex molecules with minimal off-target products. With the rapid advancement of the CC field, its applications have significantly expanded across various domains, including biomedical, pharmaceutical, radiochemistry, nanochemistry, polymer chemistry, and microscopy. However, its applications remain most prominent in medicinal chemistry. This review initially covers the introduction and distinct types of click reactions such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), strain-promoted azide-alkyne cycloaddition (SPAAC), and Diels-Alder Cycloaddition (DA), followed by the different techniques facilitating the click reactions. Among these, the CuAAC reaction is most effective and extensive CC approach widely explored for creating huge number of molecular libraries of medicinal significance due to its excellent biocompatibility, reliability, and specificity. In this review, we mainly included the synthesis and medicinal attributes of click reaction (CuAAC & SPAAC)-derived organic heterocycles from 2012-2023, particularly anticancer, antiviral, antidiabetic, and antimicrobial that will help the readers to understand the concept of CC, medicinal significance of CC-derived heterocycles, unexplored areas, challenges, and future prospects. This review will also provide a roadmap for new research directions and applications of click-derived heterocycles in medicinal chemistry.
最近,由于点击化学(CC)具有快速、可靠和生物相容性的特点,其研究迅速兴起,使其成为药物发现的理想工具。CC方法能够以最少的脱靶产物轻松且可持续地开发复杂分子。随着CC领域的快速发展,其应用已在包括生物医学、制药、放射化学、纳米化学、高分子化学和显微镜学等各个领域显著扩展。然而,其应用在药物化学中仍然最为突出。本综述首先介绍了点击反应的类型,如铜催化的叠氮化物-炔烃环加成反应(CuAAC)、应变促进的叠氮化物-炔烃环加成反应(SPAAC)和狄尔斯-阿尔德环加成反应(DA),接着介绍了促进点击反应的不同技术。其中,CuAAC反应是最有效且应用广泛的CC方法,由于其出色的生物相容性、可靠性和特异性,被广泛用于创建大量具有药用意义的分子库。在本综述中,我们主要涵盖了2012年至2023年间点击反应(CuAAC和SPAAC)衍生的有机杂环化合物的合成及其药用属性,特别是抗癌、抗病毒、抗糖尿病和抗菌方面这些将有助于读者理解CC的概念、CC衍生杂环化合物的药用意义、未探索的领域、挑战以及未来前景。本综述还将为点击衍生杂环化合物在药物化学中的新研究方向和应用提供路线图。