Ohsugi Y, Suzuki S, Takagaki Y
Cancer Res. 1976 Aug;36(8):2923-7.
Thirth-three derivatives of mycophenolic acid obtained by modifying phenolic hydroxyl and/or carboxyl groups were examined for antitumor and immunosuppressive activities. Some compounds showed more potent antitumor activities to L1210 leukemia and Ehrlich solid tumor than did mycophenolic acid. Most of these suppressed the production of antibody against sheep red blood cells in mice as strongly as did the parent substance. Correlation between antitumor and immunosuppressive activities was generally observed. However, a few compounds possessed a potent antitumor activity with less or no immunosuppressive activity.
对通过修饰酚羟基和/或羧基得到的33种霉酚酸衍生物进行了抗肿瘤和免疫抑制活性检测。一些化合物对L1210白血病和艾氏实体瘤显示出比霉酚酸更强的抗肿瘤活性。其中大多数对小鼠抗绵羊红细胞抗体产生的抑制作用与母体物质一样强。通常观察到抗肿瘤和免疫抑制活性之间存在相关性。然而,有几种化合物具有较强的抗肿瘤活性,而免疫抑制活性较弱或没有。