Vanrensburg C, Durandt C, Garlinski P, Osullivan J
NATL UNIV IRELAND UNIV COLL DUBLIN,DEPT CHEM,DUBLIN 4,IRELAND.
Int J Oncol. 1993 Nov;3(5):1011-3. doi: 10.3892/ijo.3.5.1011.
The riminophenazine agents clofazimine and its analogue B669 displayed anti-tumor activity at 30 mg/kg/day in benzo[a]pyrene (BP) induced sarcomas of mice as well as dimethylbenz-anthracene (DMBA)-induced rat mammary tumors. No hematological toxicity of these drugs at doses up to 60 mg/kg/day for one month was observed. This is the first study to document in vivo anti-neoplastic activities of clofazimine and B669.
眯吩嗪类药物氯法齐明及其类似物B669在以30毫克/千克/天的剂量给药时,对苯并[a]芘(BP)诱导的小鼠肉瘤以及二甲基苯并蒽(DMBA)诱导的大鼠乳腺肿瘤显示出抗肿瘤活性。在长达一个月的时间里,给予高达60毫克/千克/天的剂量时,未观察到这些药物有血液学毒性。这是第一项记录氯法齐明和B669体内抗肿瘤活性的研究。