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Synthesis and Antitumor Activity of Fused Quinoline Derivatives. IV. Novel 11-Aminoindolo (3, 2-b) quinolines.

…, J Ono, Y ODA, K HARADA, K HASHIGAKI…

文献索引:Takeuchi, Yasuo; Oda, Toshiaki; Chang, Ming-Rong; Okamoto, Yoko; Ono, Junko; Oda, Yoko; Harada, Kyoko; Hashigaki, Kuniko; Yamato, Masatoshi Chemical and Pharmaceutical Bulletin, 1997 , vol. 45, # 2 p. 406 - 411

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被引用次数: 23

摘要

Indolo [3, 2-b] quinoline derivatives (1) having various amine moieties were prepared and their antitumor activities against P388 leukemia in mice were evaluated, for the purpose of gaining an insight into the role of the amine moiety in the antitumor activity and searching for an effective amine moiety. Introduction of a methylene group between the phenyl group and amino or methanesulfonamido group resulted in decrease or loss of activity.