刘纪云, 张保珣, 孙家莉. 肿瘤化学治疗的研究——Ⅱ.斑蝥素衍生物和类似物的合成J. 药学学报, 1983, 18(10): 752-759.
引用本文: 刘纪云, 张保珣, 孙家莉. 肿瘤化学治疗的研究——Ⅱ.斑蝥素衍生物和类似物的合成J. 药学学报, 1983, 18(10): 752-759.
LIU Ji-yun, ZHANG Bao-xun , SUN Jia-li, . STUDIES ON A NTITUMOR CHEMOTHERAPEUTIC AGENTS——Ⅱ. SYNTHESIS OF CANTHARIDINE DERIVATIVES AND ANALOGUESJ. Acta Pharmaceutica Sinica, 1983, 18(10): 752-759.
Citation: LIU Ji-yun, ZHANG Bao-xun , SUN Jia-li, . STUDIES ON A NTITUMOR CHEMOTHERAPEUTIC AGENTS——Ⅱ. SYNTHESIS OF CANTHARIDINE DERIVATIVES AND ANALOGUESJ. Acta Pharmaceutica Sinica, 1983, 18(10): 752-759.

肿瘤化学治疗的研究——Ⅱ.斑蝥素衍生物和类似物的合成

STUDIES ON A NTITUMOR CHEMOTHERAPEUTIC AGENTS——Ⅱ. SYNTHESIS OF CANTHARIDINE DERIVATIVES AND ANALOGUES

  • 摘要: 前文报道合成了一些斑蝥素衍生物,其中羟基斑蝥胺已推荐临床试用。作者进一步改变斑蝥素结构合成了五个类型81个化合物,希望从中找到毒性低、疗效高的新抗肿瘤药,并观察化学结构与抗肿瘤活性的关系。动物筛选结果表明,该类亚胺化合物的毒性均低,除短链斑蝥亚胺化合物(66)有活性外,其余化合物均无显著抗肿瘤活性。

     

    Abstract: The preceeding paper of this series described the antitumor activity of cantharidinimide. In order to study the structure-activity relationship and further search for antitumor agent with higher activity and lower toxicity, a series of compounds with various structural modification was carried out. Eighty one derivatives of cantharidine with the following types Ⅰ, Ⅱ, Ⅲ, Ⅳ, Ⅴ were synthesized. The compounds prepared were listed in tables 1~5.Compounds 1-20 were obtained by condensation of cis-7-oxabicyclo(2,2,1) heptane-2,3-dicarboxylic anhydride with different amines in alcohol.Compounds 21-40 were carried out by condensation of bicyclo (2,2,1) heptane-2,3-dicarboxylic anhydride with pertinent amines in water or alcohol.Compounds 41-59 were prepared by condensation of desoxycantharidinimide with aliphatic amines or aromatic amines.Compounds 60-67 were synthesized by condensation of cantharidine with different amines.Compounds 68-81 were carried out by condensation of dimethylmaleic anhydride with pertinent amines in variant organic solvents.Preliminary result of animal screening showed compound 66 to be effective against mouse sarcoma 180 (ascites). Other compounds did not show any significant activity.

     

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