黄素秋, 姜照慈, 李乐真, 许静亚, 杨峻. 卟啉化合物的研究:取代四苯基卟啉与5-氟脲嘧啶共价相连化合物的合成及其抗癌活性J. 药学学报, 1991, 26(6): 415-419.
引用本文: 黄素秋, 姜照慈, 李乐真, 许静亚, 杨峻. 卟啉化合物的研究:取代四苯基卟啉与5-氟脲嘧啶共价相连化合物的合成及其抗癌活性J. 药学学报, 1991, 26(6): 415-419.
SQ Huang, ZC Jiang, LZ Li, JY Xu , J Yang, . STUDY ON PORPHYRINS:SYNTHESIS AND ANTITUMOR ACTIVITY OF PORPHYRIN-FLUOROURACIL COMPOUNDSJ. Acta Pharmaceutica Sinica, 1991, 26(6): 415-419.
Citation: SQ Huang, ZC Jiang, LZ Li, JY Xu , J Yang, . STUDY ON PORPHYRINS:SYNTHESIS AND ANTITUMOR ACTIVITY OF PORPHYRIN-FLUOROURACIL COMPOUNDSJ. Acta Pharmaceutica Sinica, 1991, 26(6): 415-419.

卟啉化合物的研究:取代四苯基卟啉与5-氟脲嘧啶共价相连化合物的合成及其抗癌活性

STUDY ON PORPHYRINS:SYNTHESIS AND ANTITUMOR ACTIVITY OF PORPHYRIN-FLUOROURACIL COMPOUNDS

  • 摘要: 合成了3个取代四苯基卟啉与5-氟脲嘧啶以共价相连的化合物。通过用它们加光照对小鼠移植瘤生长的抑制作用、对小鼠癌细胞的杀伤效果及对小鼠耳指数的测定,初步结果显示,化合物1,2,3对癌细胞都有光敏毒杀效应,但1远较2和3显著。

     

    Abstract: Three covalently linked porphyrin- fluorouracil compounds were synthesized. Measurement using these compounds for inhibition of mice transplanted tumor growth, cytotoxicity to mice cancer cells and the mice ear index under exposure to a light was performed. The results indicated that all these compounds were phototoxic to the cancer cells, and compound 1 was the most effective among them.

     

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