Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.
Molecules. 2022 Oct 29;27(21):7370. doi: 10.3390/molecules27217370.
Viral DNA and RNA polymerases are two kinds of very important enzymes that synthesize the genetic materials of the virus itself, and they have become extremely favorable targets for the development of antiviral drugs because of their relatively conserved characteristics. There are many similarities in the structure and function of different viral polymerases, so inhibitors designed for a certain viral polymerase have acted as effective universal inhibitors on other types of viruses. The present review describes the development of classical antiviral drugs targeting polymerases, summarizes a variety of viral polymerase inhibitors from the perspective of chemically synthesized drugs and natural product drugs, describes novel approaches, and proposes promising development strategies for antiviral drugs.
病毒 DNA 和 RNA 聚合酶是两种非常重要的酶,它们可以合成病毒自身的遗传物质,由于其相对保守的特性,它们已成为开发抗病毒药物的极具吸引力的靶标。不同病毒聚合酶在结构和功能上有许多相似之处,因此针对特定病毒聚合酶设计的抑制剂对其他类型的病毒也具有有效的通用抑制作用。本综述描述了针对聚合酶的经典抗病毒药物的发展,从化学合成药物和天然产物药物的角度总结了多种病毒聚合酶抑制剂,描述了新的方法,并提出了有前途的抗病毒药物开发策略。