喹唑啉
抗寄生虫的
蒂奥-
化学
二氢叶酸还原酶
组合化学
甲氨蝶呤
立体化学
生物化学
酶
生物
医学
病理
免疫学
作者
Hussein I. El‐Subbagh,Mohamed Sabry
出处
期刊:Mini-reviews in Medicinal Chemistry
[Bentham Science]
日期:2021-11-23
卷期号:21 (16): 2249-2260
被引量:7
标识
DOI:10.2174/1389557521666210304105736
摘要
Antifolates are a class of drugs used as antibacterial, antiparasitic, and anticancer agents. This review focuses on 2-substituted-mercapto-quinazolin-4(3H)-one analogues as dihydrofolatereductase (DHFR) inhibitors. Several research work have concluded a structural model for this class of 2-thio-quinazoline derivatives to get compounds with remarkable biological activity. The pattern and orientation of the p-system substitutions with regard to the quinazoline nucleus manipulate the activity. The application of the obtained model criteria produced compounds 18, 20 and 21, which proved to be 4-8 times more active than the reference drug methotrexate (MTX, 1).
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