SYNTHESIS AND ANTITUMOR-ACTIVITY OF NOVEL 6-ALKYL-6-DEMETHYLMITOMYCINS

被引:5
作者
ARAI, H
KANDA, Y
ASHIZAWA, T
MORIMOTO, M
GOMI, K
KONO, M
KASAI, M
机构
[1] KYOWA HAKKO KOGYO CO LTD,PHARMACEUT RES LABS,NAGAIZUMI,SHIZUOKA 411,JAPAN
[2] KYOWA HAKKO KOGYO CO LTD,TOKYO RES LABS,MACHIDA,TOKYO 194,JAPAN
关键词
D O I
10.1021/jm00038a009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 6-alkyl-6-demethylmitomycins (1-5) was synthesized and evaluated for anticellular and antitumor activities. These novel compounds were prepared by Michael addition of various carbanion species to 6-demethyl-7,7-(ethylenedioxy)-6,7-dihydro-6-methylidenemitosane (6 and 9) followed by treatment with NH3 or MeOH/K2CO3. Alkylation at the C-6 position of 6-demethyl-6-selenide (7) was also useful for the alternative synthesis of 6-alkyl-6-demethylmitomycins. The antitumor activity of these derivatives was evalulated, and 6-demethyl-6-ethylmitomycin A (2a) was found to exhibit excellent activity against S-180 solid tumor in mice. The structure-activity relationship is also discussed.
引用
收藏
页码:1805 / 1809
页数:5
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