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喹唑啉衍生物作为靶向化疗药物。

Quinazoline Derivatives as Targeted Chemotherapeutic Agents.

作者信息

Zayed Mohamed F

机构信息

Pharmaceutical Sciences, Fakeeh College for Medical Sciences, Jeddah, SAU.

出版信息

Cureus. 2024 May 20;16(5):e60662. doi: 10.7759/cureus.60662. eCollection 2024 May.

Abstract

Most of the current chemotherapeutic medications are extremely toxic, exhibit little selectivity, and contribute to the emergence of treatment resistance. Consequently, the discovery of targeted chemotherapy drugs with high selectivity and low side effects is necessary for cancer treatment. The quinazoline system has a broad range and a long history of biological activities. Numerous quinazoline derivatives have been used to treat different types of cancer by working on various molecular targets. This review presents various chemical information, including molecular structure, design, and biological activity of some reported quinazolines that function by inhibiting four types of important molecular targets: dihydrofolate reductase, breast cancer resistant protein, poly-(ADP-ribose)-polymerase, and tubulin polymerization.

摘要

目前大多数化疗药物毒性极强,选择性差,并会导致耐药性的产生。因此,开发高选择性、低副作用的靶向化疗药物对于癌症治疗至关重要。喹唑啉类化合物具有广泛的生物活性,其研究历史悠久。众多喹唑啉衍生物通过作用于各种分子靶点,已被用于治疗不同类型的癌症。本综述介绍了一些已报道的喹唑啉类化合物的各种化学信息,包括分子结构、设计以及生物活性,这些喹唑啉类化合物通过抑制四种重要分子靶点发挥作用,即二氢叶酸还原酶、乳腺癌耐药蛋白、聚(ADP - 核糖)聚合酶和微管蛋白聚合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b74/11186210/9ec32b66dbd1/cureus-0016-00000060662-i01.jpg

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