化学
广谱
组合化学
纳米技术
生化工程
材料科学
工程类
作者
Pankaj V. Ledade,Trimurti L. Lambat,Jitendra K. Gunjate,P Chopra,Amitkumar V. Bhute,Mamata R. Lanjewar,Pooja M. Kadu,Utpal Dongre,Sami H. Mahmood
标识
DOI:10.2174/1385272827666221227120648
摘要
Abstract: The fused Nitrogen heterocyclic compounds and their derivatives have grown in prominence over the past several decades as a result of their significant medical value. The adaptable and easily synthesized N-Heterocyclic scaffolds are particularly exciting in both synthetic organic chemistry and the biological sector due to their powerful pharmacological properties, which are taken into consideration while considering their numerous uses. For the synthesis of N-heterocycles and their derivatives, several attempts were undertaken to create a variety of synthetic protocols. The N-Heterocyclic compounds provide a variety of adaptable structures for specific biological applications and represent novel, broad-spectrum antibacterial and anticancer agents. They typically have minimal toxicity profiles. The majority of these N-Heterocycles have demonstrated more cytotoxicity than the effective anticancer medication cisplatin. The design, synthesis, structural characterisation, and biological uses of N-Heterocycles are reviewed in this work. In this article, the developments made in this specific field are comprehensively examined.
科研通智能强力驱动
Strongly Powered by AbleSci AI