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喹啉作为癌症药物发现中一种优势骨架的概述。

An overview of quinoline as a privileged scaffold in cancer drug discovery.

作者信息

Musiol Robert

机构信息

a Institute of Chemistry , University of Silesia in Katowice , Katowice , Poland.

出版信息

Expert Opin Drug Discov. 2017 Jun;12(6):583-597. doi: 10.1080/17460441.2017.1319357. Epub 2017 Apr 20.

Abstract

The concept of privileged structures is well known and is often used in the process of drug design and development. Although its assumptions are not clear, its overall usefulness remains high. Various substructures have been identified as privileged and quinoline is a prime example of such a structure. Areas covered: Quinoline drugs that are currently approved or under clinical investigation were reviewed based on a literature search. Their modes of action and outcomes during clinical research are discussed. Expert opinion: Undoubtedly, quinoline-based compounds have a significant impact on anticancer drugs. Although topoisomerase and kinase inhibitors are the only two different classes of agents that are currently approved for anticancer therapy, more than twenty different drug candidates are being tested on humans. The quinoline moiety offers an easily accessible, well-understood scaffold for designing new drugs. It is also a very druggable molecule with the potency for structure optimization through established synthetic pathways. For these reasons, quinoline-based anticancer drugs have a strong position in modern medicinal chemistry.

摘要

特权结构的概念广为人知,且常用于药物设计与开发过程中。尽管其假设并不明确,但其整体实用性依然很高。各种子结构已被确定为具有特权的结构,喹啉就是这种结构的一个典型例子。涵盖领域:通过文献检索对目前已获批或正在进行临床研究的喹啉类药物进行了综述。讨论了它们在临床研究中的作用模式和结果。专家观点:毫无疑问,基于喹啉的化合物对抗癌药物有重大影响。尽管拓扑异构酶和激酶抑制剂是目前仅有的两类获批用于抗癌治疗的药物,但有二十多种不同的候选药物正在进行人体试验。喹啉部分为新药设计提供了一个易于获取且理解透彻的骨架。它也是一个极具成药性的分子,有通过既定合成途径进行结构优化的潜力。基于这些原因,基于喹啉的抗癌药物在现代药物化学中占据重要地位。

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