Yoshida M, Hoshi A, Kuretani K, Kanai T, Ichino M
Gan. 1975 Oct;66(5):561-4.
Effect of substitution of 5-position of cyclocytidine with fluorine on its antitumor activity in cultured cells was examined. 5-Fluorocyclocytidine was active against cultured L-5178Y cells similar to cyclocytidine. IC50 of the compound was 0.054 mug/ml. This compound inhibited thymidine incorporation into acid-soluble fraction of the cells. Cell growth inhibition by 5-fluorocyclocytidine was reversed by deoxycytidine but not by thymidine and deoxyuridine. On the other hand, cell growth inhibition by 5-fluorouracil was reversed by thymidine and deoxyuridine. As a result, site of action of 5-fluorocyclocytidine was considered to be similar to that of cyclocytidine and not to 5-fluorouracil.
研究了环胞苷5位用氟取代对其在培养细胞中抗肿瘤活性的影响。5-氟环胞苷对培养的L-5178Y细胞具有活性,与环胞苷相似。该化合物的IC50为0.054微克/毫升。此化合物抑制胸苷掺入细胞的酸溶性部分。5-氟环胞苷对细胞生长的抑制作用可被脱氧胞苷逆转,但不能被胸苷和脱氧尿苷逆转。另一方面,5-氟尿嘧啶对细胞生长的抑制作用可被胸苷和脱氧尿苷逆转。结果,认为5-氟环胞苷的作用位点与环胞苷相似,而与5-氟尿嘧啶不同。