Houlihan W J, Munder P G, Handley D A, Nemecek G A
Atherosclerosis and Vascular Biology, Preclinical Research, Sandoz Pharmaceuticals Corporation, East Hanover, NJ USA.
Arzneimittelforschung. 1995 Oct;45(10):1133-7.
SDZ 62-434 (CAS 115621-95-9, 5-(4'-piperidinomethylphenyl)-2,3-dihydroimidazo [2,1-a]isoquinoline dihydrochloride), a member of a novel class of antitumor agents, exhibited direct and macrophage-induced cytotoxicity against a variety of murine tumor cell lines. It is more effective than edelfosine in increasing survivors and reducing tumor volume in the oral mouse Meth A fibrosarcoma model. Preliminary studies suggest that an undefined cytotoxic effect, macrophage activation and possible effects on signal transduction may account for its antitumor mechanism of action. SDZ 62-434 is currently in Phase I clinical trials as a potential antitumor agent.
SDZ 62 - 434(化学物质登记号115621 - 95 - 9,5 -(4'-哌啶甲基苯基)- 2,3 -二氢咪唑并[2,1 - a]异喹啉二盐酸盐)是一类新型抗肿瘤药物中的一种,对多种小鼠肿瘤细胞系表现出直接的以及巨噬细胞诱导的细胞毒性。在口服给药的小鼠甲基胆蒽诱导的A系纤维肉瘤模型中,它在增加存活动物数量和减小肿瘤体积方面比依地福新更有效。初步研究表明,一种未明确的细胞毒性作用、巨噬细胞激活以及对信号转导的可能影响可能是其抗肿瘤作用机制。SDZ 62 - 434作为一种潜在的抗肿瘤药物目前正处于I期临床试验阶段。