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新型多拉司他汀10类似物的合成及其抗肿瘤活性

Synthesis and antitumor activity of novel dolastatin 10 analogs.

作者信息

Miyazaki K, Kobayashi M, Natsume T, Gondo M, Mikami T, Sakakibara K, Tsukagoshi S

机构信息

Research Department, Teikoku Hormone Mfg. Co., Ltd., Kawasaki, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1995 Oct;43(10):1706-18. doi: 10.1248/cpb.43.1706.

Abstract

Dolastatin 10 (1) is a potent antineoplastic pentapeptide. Novel dolastatin 10 analogs each modified at one of the constituent amino acid derivatives, were synthesized and their antitumor activity was evaluated against P388 leukemia in mice. The structural requirements for antitumor activity are discussed. Some of the analogs, 31c, 35c, 38b, and 50c showed excellent activity in vivo. Highly active 50c, which lacks the thiazole group of 1, was selected for further development as an antitumor agent.

摘要

多拉司他汀10(1)是一种强效抗肿瘤五肽。合成了在其中一种组成氨基酸衍生物上进行修饰的新型多拉司他汀10类似物,并评估了它们对小鼠P388白血病的抗肿瘤活性。讨论了抗肿瘤活性的结构要求。一些类似物,31c、35c、38b和50c在体内表现出优异的活性。选择了缺乏1的噻唑基团的高活性50c作为抗肿瘤药物进行进一步开发。

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