Citarella R V, Wallace R E, Murdock K C, Angier R B, Durr F E, Forbes M
Cancer Res. 1982 Feb;42(2):440-4.
9,10-Anthracenedicarboxaldehyde bis[(4,5-dihydro-1H-imidazol-2-yl)hydrazone] dihydrochloride (CL 216942; bisantrene hydrochloride; NSC 337766), a member of a new chemical class of compounds with antineoplastic properties, has been evaluated for antitumor activity in experimental murine tumor systems. The compound produced significant increases in life span (LS) and long-term survivors among mice bearing transplantable leukemias and solid tumors. Optimal treatment regimens resulted in an ILS of greater than 173 and 151% in mice with P388 and L1210 leukemia, respectively, an ILS of greater than 85% in mice with Lieberman plasma cell tumor, and an ILS of greater than 200, 150, and 63%, respectively, in mice with B16 melanoma, colon tumor 26, and Ridgway osteogenic sarcoma. An adriamycin-resistant subline of P388 leukemia showed complete cross-resistance to CL of 216942. The compound was active when administered by the i.p., i.v., and s.c. routes, but p.o. activity was not observed. Significant schedule dependency was not observed when the drug was administered once daily for 9 days, once every 4 days, or as a single dose, but single doses typically produced the best effects. CL 216942 was a potent inhibitor of DNA and RNA synthesis in L5178Y lymphoma cells cultured in vitro, and preliminary studies indicated the drug was a DNA-intercalating agent. The drug was cytotoxic for rapidly proliferating and nonproliferating (G0) human colon carcinoma WiDR cells in vitro.U
9,10-蒽二甲醛双[(4,5-二氢-1H-咪唑-2-基)腙]二盐酸盐(CL 216942;双胺苯吖啶盐酸盐;NSC 337766)是一类具有抗肿瘤特性的新型化合物,已在实验性小鼠肿瘤系统中评估其抗肿瘤活性。该化合物使患有可移植白血病和实体瘤的小鼠的生存期(LS)显著延长,长期存活者数量增加。最佳治疗方案使患有P388和L1210白血病的小鼠的ILS分别大于173%和151%,患有Lieberman浆细胞瘤的小鼠的ILS大于85%,患有B16黑色素瘤、结肠肿瘤26和Ridgway骨肉瘤的小鼠的ILS分别大于200%、150%和63%。P388白血病的阿霉素耐药亚系对CL 216942表现出完全交叉耐药。该化合物经腹腔注射、静脉注射和皮下注射给药时具有活性,但口服无活性。当药物每日给药1次,共9天、每4天给药1次或单次给药时,未观察到显著的给药方案依赖性,但单次给药通常产生最佳效果。CL 216942是体外培养的L5178Y淋巴瘤细胞中DNA和RNA合成的强效抑制剂,初步研究表明该药物是一种DNA嵌入剂。该药物在体外对快速增殖和非增殖(G0)的人结肠癌细胞WiDR具有细胞毒性。