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5-氟尿嘧啶的1-烷基氨基甲酰基衍生物在多种小鼠肿瘤中的抗肿瘤活性。

Antitumor activity of 1-alkylcarbamoyl derivatives of 5-fluorouracil in a variety of mouse tumors.

作者信息

Iigo M, Hoshi A, Nakamura A, Kuretani K

出版信息

Cancer Chemother Pharmacol. 1978;1(4):203-8. doi: 10.1007/BF00257150.

Abstract

The antitumor properties of 1-alkylcarbamoyl derivatives of 5-fluorouracil were examined in various mouse tumor systems to select promising compounds for clinical use. Almost all alkylcarbamoyl derivatives were active against various tumors when given by oral administration. Among them, 1-methyl, 1-ethyl, 1-isopropyl, 1-hexyl and 1-octyl carbamoyl derivatives of 5-fluorouracil were moderately or markedly active in six mouse tumor systems tested. However, 1-methyl, 1-ethyl, and 1-isopropyl carbamoyl derivatives were toxic to mice, though not lethal. As a result, 1-hexyl and 1-octyl carbamoyl derivatives were selected as the best candidates for antitumor agents in further study.

摘要

在多种小鼠肿瘤模型中研究了5-氟尿嘧啶的1-烷基氨基甲酰基衍生物的抗肿瘤特性,以筛选出有临床应用前景的化合物。几乎所有的烷基氨基甲酰基衍生物经口服给药后对多种肿瘤均有活性。其中,5-氟尿嘧啶的1-甲基、1-乙基、1-异丙基、1-己基和1-辛基氨基甲酰基衍生物在六个测试的小鼠肿瘤模型中表现出中度或显著活性。然而,1-甲基、1-乙基和1-异丙基氨基甲酰基衍生物对小鼠有毒性,但不致命。因此,1-己基和1-辛基氨基甲酰基衍生物被选为进一步研究中抗肿瘤药物的最佳候选物。

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