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其他丝裂霉素 A 类似物的制备及其抗肿瘤活性

Preparation and antitumor activity of additional mitomycin A analogues.

作者信息

Sami S M, Remers W A, Bradner W T

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Arizona, Tucson 85721.

出版信息

J Med Chem. 1989 Mar;32(3):703-8. doi: 10.1021/jm00123a036.

Abstract

On the basis of qualitative structure-activity relationships developed in the preceding article, a series of 32 new mitomycin A analogues were prepared and tested in antitumor screens. Seven of them gave greater prolongation of life (ILS) than mitomycin C in the mouse P388 leukemia assay. They included examples with 7-O substituents such as cyclic ethers and nitrogen heterocycles. A Hansch analysis was attempted with log P and MR as the independent variables, but no statistically significant correlation could be made. Seven compounds, chosen mainly for their good potency (MED), were tested in the subcutaneous B16 melanoma assay in mice and four of them showed greater ILS than mitomycin C.

摘要

基于前文所建立的定性构效关系,制备了一系列32种新的丝裂霉素A类似物,并在抗肿瘤筛选中进行了测试。在小鼠P388白血病试验中,其中7种类似物比丝裂霉素C能更显著地延长生存期(ILS)。它们包括具有7-O取代基的例子,如环醚和氮杂环。尝试以log P和MR作为自变量进行Hansch分析,但未得出具有统计学意义的相关性。主要因其良好的效力(MED)而选择的7种化合物在小鼠皮下B16黑色素瘤试验中进行了测试,其中4种显示出比丝裂霉素C更高的ILS。

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