β-内酰胺和尿素作为原核系统的交叉抑制剂

M. Konaklieva, B. Plotkin
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引用次数: 0

摘要

近三十年来,β-内酰胺被认为是原核和真核系统中丝氨酸和半胱氨酸酶的通用酰化剂。最近,COVID-19大流行推动了它们的使用,从而扩大了它们作为病毒酶抑制剂的应用范围。以尿素为基础的药物作为上述酶的抑制剂已被广泛研究。本综述的重点是过去十年的药物发现策略,以及在开发新的抗菌和抗病毒药物中扩大β-内酰胺和脲类药物的新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
β-Lactams and Ureas as Cross Inhibitors of Prokaryotic Systems
β-Lactams in the last thirty years have been viewed as universal acylating agents of serine and cysteine enzymes of both prokaryotic and eukaryotic systems. More recently, their use has been propelled by the COVID-19 pandemic, thus broadening their application as inhibitors of viral enzymes. The urea-based drugs have been extensively studied as inhibitors of the aforementioned enzymes. The focus of this review is the last decade’s drug discovery strategies, as well as new strategies that show utility in the expansion of β-lactams and ureas in the development of new antimicrobial and antiviral drugs.
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