5-[(AMINOALKYL)AMINO]IMIDAZO[4,5,1-DE]ACRIDIN-6-ONES AS A NOVEL CLASS OF ANTINEOPLASTIC AGENTS - SYNTHESIS AND BIOLOGICAL-ACTIVITY

被引：106

作者：

CHOLODY, WM ^{[1
]}

MARTELLI, S ^{[1
]}

PARADZIEJLUKOWICZ, J ^{[1
]}

KONOPA, J ^{[1
]}

机构：

[1] UNIV CAMERINO,DEPT CHEM SCI,I-62032 CAMERINO,ITALY

来源：

JOURNAL OF MEDICINAL CHEMISTRY | 1990年 / 33卷 / 01期

关键词：

D O I：

10.1021/jm00163a009

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

A new class of antineoplastic agents, the 5-substituted imidazo[4,5,1-de]acridin-6-ones with an (aminoalkyl)amino group in the side chain, has been made. These compounds were synthesized by reduction of 1-substituted 4-nitroacridin-9(10H)-ones and subsequent reaction of the derived amines with carboxylic acids. Their cytotoxic activity against HeLaS3cells in tissue culture and in vivo antitumor activity against P388 leukemia in mice was demonstrated. A strict relationship between the antineoplastic activity and the number of methylene spacers between proximal and distal nitrogens in the side chain was established. © 1990, American Chemical Society. All rights reserved.

引用

页码：49 / 52

页数：4

共 29 条

[1] RING-HYDROXYLATED ANALOGS OF LUCANTHONE AS ANTI-TUMOR AGENTS [J].