四氢黄连碱型季铵化合物的合成及生物活性研究
Synthesis and biological evaluation of tetrahydrocoptisine quaternary ammonium compounds
-
摘要:
为评价四氢黄连碱型季铵化合物降血糖、降血脂的作用, 本文以盐酸黄连碱 (2) 为起始原料, 经硼氢化钠还原得到四氢黄连碱, 再对其进行季铵化衍生, 合成了15个新型黄连碱衍生物4~18, 通过1H NMR、HR-MS进行了化学结构确证, 并在HepG2细胞葡萄糖消耗模型上评价了所有化合物体外促葡萄糖消耗活性。对于活性较好的化合物进一步评价了其体内降血脂活性。结果表明: 化合物5、7、8、9表现出了较好的体外促葡萄糖消耗活性, 化合物5、8在高脂血症小鼠和金黄地鼠模型上显示出较好的体内降血脂活性, 但作用效果没有阳性对照药辛伐他汀显著。
Abstract:The goal of treatment of metabolic syndrome is the prevention of diabetes and cardiovascular events. A series of novel tetrahydrocoptisine quaternary ammonium compounds were prepared to evaluate their action of hypoglycemia and hypolipidemia for finding the therapeutic agents of metabolic syndrome. Starting from the coptisine hydrochloride (2), fifteen target compounds were synthesized by reduction and substitution of the 7-N position. All of the target compounds were characterized by 1H NMR and HR-MS. Their hypoglycemic activities were evaluated in HepG2 cell and hypolipidemic activities of compounds with better hypoglycemic activity were tested further in vivo. Results indicated that compounds 5, 7, 8 and 9 exhibited better hypoglycemic activities in vitro and compounds 5 and 8 exhibited good hypolipidemic activities in high-fat-diet (HFD) induced hyperlipidemia mice and (or) hamsters. However, the activity is not as good as simvastatin.
下载: