Synthetic and Pharmacological Expedition of Pyrazolo[1,5-a]pyridine: A Comprehensive Review

N. Agrawal, Dimple Bansal, V. Gautam
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引用次数: 0

Abstract

Fused nitrogen-containing heterocyclic compounds have been identified to display a prominent role in medicinal chemistry, biochemistry, and other streams of science. Countless derivatives of pyrazolo[1,5-a] pyridine have been investigated by researchers for their distinct pharmacological characterization. In this article, we have revealed and arranged the various routes of synthesis and therapeutic activities such as dopamine binding affinity, kinase inhibitory activity, and PDE inhibitors of pyrazolo[1,5-a]pyridine-containing compounds which have been explored till now. The remarkable outcomes obtained via in vitro as well as in vivo profile screening of this moiety and its derivatives lead this scaffold to be recognized to a greater extent and examined further for better results. This review will give medicinal chemists a flying-bird eye catch view of pyrazolo[1,5-a] pyridine derivatives which will help them to design and synthesize potential compounds bearing this moiety.
吡唑啉[1,5- A]吡啶的合成及药理研究综述
融合含氮杂环化合物已被确定在药物化学,生物化学和其他科学流中显示出突出的作用。研究人员对吡唑[1,5-a]吡啶的无数衍生物进行了研究,因为它们具有独特的药理特征。在本文中,我们揭示并整理了迄今为止探索的吡唑[1,5-a]吡啶类化合物的各种合成途径及其多巴胺结合亲和力、激酶抑制活性、PDE抑制剂等治疗活性。通过对该片段及其衍生物的体外和体内筛选获得的显著结果使该支架得到更大程度的识别,并进一步研究以获得更好的结果。这一综述将使药物化学家对吡唑[1,5-a]吡啶衍生物有一个全面的了解,这将有助于他们设计和合成含有该片段的潜在化合物。
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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