Journal of medicinal chemistry

Hexahydropyrimidines. IV. 1 Synthesis of 2-[4-(N, N-Bis (2-chloroethyl) amino) aryl]-1, 3-bis-(aralkyl) hexahydropyrimidines as Antitumor Agents2

JH Billman, JL Meisenheimer

文献索引：Billman,J.H.; Meisenheimer,J.L. Journal of Medicinal Chemistry, 1964 , vol. 7, p. 115 - 117

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被引用次数: 8

摘要

. I wide range of activity was obtained by varying thr substituents.-\ r in the I? Ia structure from p-methoxyphenyl (100%) inhibition at 100 mg./kg.) to p-chlorophenyl (71% inhibition at 100 mg./kg.) to 2, 1-dichlorophenyl (" 2% inhibition at 100 mg./kg.). These substituents established the same relative order of activity in thr J'IIb series. The markedly increased antitumor activity thus appears to be related to electroil donors on the benzyl group, even ...