Pour P, Althoff J, Gingell R, Kupper R
Cancer Lett. 1976 Mar;1(4):197-202. doi: 10.1016/s0304-3835(75)96702-6.
Weekly subcutaneous injection of N-nitroso-bis(2-acetoxypropyl)amine (BAP) for 20 weeks to Syrian golden hamsters induced pancreatic neoplasms in 50% of the animals, as early as 15 weeks from the start of treatment. The carcinogenic potency and organotropic spectrum of BAP were similar to those of N-nitroso-bis(2-hydroxypropyl)amine (BHP). Metabolism studies indicated that BAP was readily converted in vivo to BHP and that BHP was also the major urinary metabolite.
对叙利亚金黄地鼠每周皮下注射N-亚硝基双(2-乙酰氧基丙基)胺(BAP),持续20周,早在治疗开始后15周,50%的动物诱发了胰腺肿瘤。BAP的致癌效力和器官otropic谱与N-亚硝基双(2-羟丙基)胺(BHP)相似。代谢研究表明,BAP在体内很容易转化为BHP,并且BHP也是主要的尿液代谢产物。