Functionalized Benzisoxazoles: Recent Developments in Diversified Synthetic Strategies and Cytotoxic Potential

IF 3.5 3区 医学 Q2 CHEMISTRY, MEDICINAL
Shibangi Bhattacharjee, Nayanita Chakraborty, Rajesh Tiwari, Kamya Goyal, Vikramdeep Monga
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引用次数: 0

Abstract

Benzisoxazoles are pivotal heterocyclic scaffolds that have emerged as focal points in both synthetic and medicinal chemistry due to their broad synthetic applications and a wide spectrum of pharmacological properties. Their unique structural framework, along with the presence of an oxygen–nitrogen bond within a fused bicyclic ring system, confers remarkable physicochemical and biological properties, including anticancer, antibacterial, antifungal, antiviral, anti-inflammatory and diuretic activities. Appropriately constructed benzisoxazole scaffolds display remarkable potential to interact with a broad range of biological targets, thereby offering significant opportunities for the development of novel therapeutic agents with diverse mechanisms of action. Chemists have been intrigued by the fascinating properties of benzisoxazoles, and extensive scientific studies have been carried out to integrate the benzisoxazole scaffold into various bioactive compounds, including complex molecular frameworks. The past few years have witnessed tremendous progress in the development of various multicomponent one-pot synthetic strategies, including transition-metal catalysis, metal-free cyclization and microwave-assisted synthesis for diversely substituted benzisoxazole derivatives. This review highlights recent advancements in the synthetic chemistry of functionalized benzisoxazoles, including marketed drugs and agents in clinical trials. Furthermore, recent developments in the medicinal chemistry of benzisoxazole derivatives as anticancer agents, encompassing their mechanistic aspects, structure-activity relationships, and in silico studies, have been compiled. Drawing on the literature, the authors aim to provide a broad perspective and valuable insights for researchers, thereby inspiring and accelerating the development of novel benzisoxazole-appended anticancer therapeutics with significant biological implications.

功能化苯并异恶唑:多样化合成策略和细胞毒性潜能的最新进展。
苯并异恶唑是重要的杂环支架,由于其广泛的合成应用和广泛的药理性质,已成为合成和药物化学的焦点。它们独特的结构框架,以及在融合双环系统中存在的氧-氮键,赋予了显著的物理化学和生物特性,包括抗癌、抗菌、抗真菌、抗病毒、抗炎和利尿活性。适当构建的苯并恶唑支架显示出与广泛的生物靶点相互作用的巨大潜力,从而为开发具有多种作用机制的新型治疗剂提供了重要的机会。化学家们一直被苯并恶唑的迷人特性所吸引,并进行了广泛的科学研究,将苯并恶唑支架整合到各种生物活性化合物中,包括复杂的分子框架。近年来,在过渡金属催化、无金属环化和微波辅助合成多取代苯并恶唑衍生物等多组分一锅法合成策略方面取得了巨大进展。本文综述了功能化苯并异恶唑合成化学的最新进展,包括已上市的药物和临床试验中的药物。此外,最近发展的药物化学苯并恶唑衍生物作为抗癌剂,包括其机制方面,结构-活性关系,并在硅研究,已汇编。通过对相关文献的分析,作者希望为研究人员提供一个广阔的视角和有价值的见解,从而激发和加速新型苯并恶唑抗癌药物的开发,并具有重要的生物学意义。
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
Archiv der Pharmazie
Archiv der Pharmazie 医学-化学综合
CiteScore
7.90
自引率
5.90%
发文量
176
审稿时长
3.0 months
期刊介绍: Archiv der Pharmazie - Chemistry in Life Sciences is an international journal devoted to research and development in all fields of pharmaceutical and medicinal chemistry. Emphasis is put on papers combining synthetic organic chemistry, structural biology, molecular modelling, bioorganic chemistry, natural products chemistry, biochemistry or analytical methods with pharmaceutical or medicinal aspects such as biological activity. The focus of this journal is put on original research papers, but other scientifically valuable contributions (e.g. reviews, minireviews, highlights, symposia contributions, discussions, and essays) are also welcome.
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