Potential central nervous system antitumor agents. Aziridinylbenzoquinones. 2
作者:Feng-Te Chou、A. Hameed Khan、John S. Driscoll
DOI:10.1021/jm00233a010
日期:1976.11
derivatives was synthesized and evaluated as central nervous system antitumor agents in the murine intracerebral L1210 and ependymoblastoma brain tumor systems. Intraperitoneal activity was evaluted in the leukemia L1210, P388, and B16 melanocarcinoma tumor models. The more hydrophilic hydroxyalkylamino compounds were the most effective in the intraperitoneal ascites systems (L1210, P388) with the dihydroxypropylamino
合成了一系列15种2,5,2-二氮杂吡啶基-3,6-双(烷基氨基)-1,4-苯醌衍生物,并作为鼠脑L1210和上皮成纤维细胞瘤脑肿瘤系统的中枢神经系统抗肿瘤药进行了评估。在白血病L1210,P388和B16黑色素瘤肿瘤模型中评估了腹膜内活性。亲水性更高的羟烷基氨基化合物在腹水腹水系统(L1210,P388)中最有效,二羟丙基氨基(18)和羟乙基氨基(17)类似物可以长期存活。简单的,更具亲脂性的单和二烷基氨基衍生物在脑系统中最有效。在上皮细胞母细胞瘤脑肿瘤系统中,使用甲基(13),乙基(14)和二甲基氨基(20)化合物获得了多个长期存活者。母体氨基类似物12在几种肿瘤模型中非常活跃。讨论了结构,活性和水溶性之间的关系。