Andreani A, Bossa R, Fraccari A, Galatulas I, Ninci M A, Rambaldi M
Dipartimento di Scienze Farmaceutiche dell'Università, Bologna, Italy.
Anticancer Res. 1996 Jul-Aug;16(4A):1831-3.
Synthesis of 2,6-Bis[bis(2-chloroethyl)amino]-4,8-dipiperidino-pyrimido [5,4-d]pyrimidine (DIP-C1) was carried out, and the new derivative showed cytotoxic activity comparable to other alkylating drugs on cultured P388 leukaemia cells and HeLa cells. The present paper reports the effects of DIP-C1 on respiration of Ehrlich ascites tumor cells and on survival of the mice implanted with Ehrlich ascites tumor cells. The compound showed a significant activity in both experimental models.
合成了2,6-双[双(2-氯乙基)氨基]-4,8-二哌啶基嘧啶并[5,4-d]嘧啶(DIP-C1),该新衍生物在培养的P388白血病细胞和HeLa细胞上表现出与其他烷化剂相当的细胞毒性活性。本文报道了DIP-C1对艾氏腹水瘤细胞呼吸及对植入艾氏腹水瘤细胞的小鼠存活情况的影响。该化合物在两个实验模型中均显示出显著活性。