Medicinal Chemistry of Quinazolines as Anticancer Agents Targeting Tyrosine Kinases

IF 2.3 Q3 PHARMACOLOGY & PHARMACY
M. Zayed
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引用次数: 3

Abstract

Cancer is a large group of diseases that can affect any organ or body tissue due to the abnormal cellular growth with the unknown reasons. Many of the existing chemotherapeutic agents are highly toxic with a low level of selectivity. Additionally, they lead to development of therapeutic resistance. Hence, the development of targeted chemotherapeutic agents with low side effects and high selectivity is required for cancer treatment. Quinazoline is a vital scaffold well-known to be linked with several biological activities. The anticancer activity is one of the prominent biological activities of this scaffold. Several established anticancer quinazolines work by different mechanisms on the various molecular targets. The aim of this review is to present different features of medicinal chemistry as drug design, structure activity relationship, and mode of action of some targeted anticancer quinazoline derivatives. It gives comprehensive attention on the chemotherapeutic activity of quinazolines in the viewpoint of drug discovery and its development. This review provides panoramic view to the medicinal chemists for supporting their efforts to design and synthesize novel quinazolines as targeted chemotherapeutic agents.
靶向酪氨酸激酶的喹唑啉类抗癌药物的药物化学研究
癌症是由于细胞生长异常,原因不明,可影响任何器官或身体组织的一大类疾病。现有的许多化疗药物毒性大,选择性低。此外,它们还会导致治疗耐药性的产生。因此,开发低副作用、高选择性的靶向化疗药物是癌症治疗的需要。喹唑啉是一种重要的支架,已知与几种生物活性有关。抗癌活性是该支架突出的生物活性之一。几种已建立的抗癌喹唑啉通过不同的机制作用于不同的分子靶点。本文综述了一些靶向抗癌喹唑啉衍生物在药物化学方面的不同特点,如药物设计、结构活性关系和作用方式。本文从药物发现和开发的角度全面介绍了喹唑啉类药物的化疗活性。本文综述为药物化学家设计和合成新型喹唑啉类靶向化疗药物提供了参考。
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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来源期刊
Scientia Pharmaceutica
Scientia Pharmaceutica Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.60
自引率
4.00%
发文量
67
审稿时长
10 weeks
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