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首页> 外文期刊>Journal of Medicinal Chemistry >The Alpha Keto Amide Moiety as a Privileged Motif in Medicinal Chemistry: Current Insights and Emerging Opportunities
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The Alpha Keto Amide Moiety as a Privileged Motif in Medicinal Chemistry: Current Insights and Emerging Opportunities

机译:Alpha Keto酰胺部分作为药物化学的特权主题:当前的见解和新兴机会

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Over the years, researchers in drug discovery have taken advantage of the use of privileged structures to design innovative hit/lead molecules. The a-ketoamide motif is found in many natural products, and it has been widely exploited by medicinal chemists to develop compounds tailored to a vast range of biological targets, thus presenting clinical potential for a plethora of pathological conditions. The purpose of this perspective is to provide insights into the versatility of this chemical moiety as a privileged structure in drug discovery. After a brief analysis of its physical-chemical features and synthetic procedures to obtain it, alpha-ketoamide-based classes of compounds are reported according to the application of this motif as either a nonreactive or reactive moiety. The goal is to highlight those aspects that may be useful to understanding the perspectives of employing the alpha-ketoamide moiety in the rational design of compounds able to interact with a specific target.
机译:多年来,药物发现领域的研究人员利用特权结构设计出创新的击中/引导分子。a-酮酰胺基序存在于许多天然产物中,药物化学家已广泛利用该基序开发出适合多种生物靶标的化合物,从而为过多的病理条件提供了临床潜力。这一观点的目的是提供对这种化学成分作为药物发现中的特权结构的多功能性的见解。在简要分析其物理化学特征和合成步骤以获得它之后,根据该基序作为非反应性或反应性部分的应用,报道了基于α-酮酰胺的化合物类别。目的是强调那些可能有助于理解在合理设计能够与特定目标相互作用的化合物时使用α-酮酰胺部分的观点的方面。

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