摘要
目的:定位合成6-O-丙酰基日本杜鹃素Ⅲ,评价其毒性。方法:以日本杜鹃素Ⅲ为原料合成目标物,用小鼠测定LD50。结果:获得目标物并测得LD_(50)=2.51mg/kg(可信限2.0~3.19)。结论:日本杜鹃素Ⅲ经6-O-丙酰化后,毒性降低5倍。
OBJECTIVE:To synthesize the rhodojaponin Ⅲ 6-propionate and evaluate its toxicity,METHOD:We used rhodojaponin Ⅲ as raw material and mice as experimental animals。 RESULTS:The title compound and itsLD50=2.5l mg/kg(confidence limit is 2.0~3. 19)were obtained.CONCLUSION The toxicity of rhodojaponin Ⅲ6-propionate is five times smaller than that of rhodojaponin Ⅲ.
出处
《中国药学杂志》
CAS
CSCD
北大核心
1996年第12期752-753,共2页
Chinese Pharmaceutical Journal