Abu-Melha Sraa
Acta Chim Slov. 2017 Dec;64(4):919-930. doi: 10.17344/acsi.2017.3617.
A series of substituted 1,8-naphthyridine derivatives was synthesized to be used as cytotoxic and antioxidant agents by applying 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carbohydrazide (1) as the starting material. Compound 1 was reacted with different reagents to afford the corresponding 3-heterarylcarbonyl-1,8-naphthyridine derivatives 3-19 which were tested for their in vitro cytotoxicity against Ehrlich Ascites Carcinoma, and antioxidant activity. Compound 15 showed the best cytotoxicity and antioxidant activity.
以1,4 - 二氢 - 4 - 氧代 - 1,8 - 萘啶 - 3 - 碳酰肼(1)为起始原料,合成了一系列取代的1,8 - 萘啶衍生物,用作细胞毒性剂和抗氧化剂。化合物1与不同试剂反应,得到相应的3 - 杂芳基羰基 - 1,8 - 萘啶衍生物3 - 19,并对其针对艾氏腹水癌的体外细胞毒性和抗氧化活性进行了测试。化合物15表现出最佳的细胞毒性和抗氧化活性。