Synthesis and Hypolipidemic Activities of Novel 2-[4-[(Diethoxyphosphoryl)methyl]phenyl]quinazolines and 4(3<i>H</i>)-Quinazolinones
作者:Yasuhisa Kurogi、Yasuhide Inoue、Kazuhiko Tsutsumi、Shizuo Nakamura、Kazushi Nagao、Hiroki Yoshitsugu、Yoshihiko Tsuda
DOI:10.1021/jm9506938
日期:1996.1.1
Derivatives bearing a 4-[(diethoxyphosphoryl)-methyl]phenyl] group at the 2-position were found to lower triglyceride and total cholesterol levels. In accord with the decrease in log P*, quinazolines and 4(3H)-quinazolinones showed good absorption and hypolipidemic activity. When the quinazolinone ring system is substituted at positions 6 and 7 with methoxy groups, increased hypolipidemic activity was observed
新型化合物NO-1886,4-[((二乙氧基磷酰基)甲基] -N-(4-溴-2-氰基苯基)-苯甲酰胺,是一种降血脂药,似乎增加了大鼠脂蛋白脂肪酶的活性。合成了NO-1886的各种类似物,以研究这种降血脂药的构效关系。通过环化NO-1886衍生物制备了一系列新的喹唑啉和4(3H)-喹唑啉酮。发现在2-位带有4-[((二乙氧基磷酰基)-甲基]苯基]基团的衍生物降低甘油三酸酯和总胆固醇水平。与log P *的降低一致,喹唑啉和4(3H)-喹唑啉酮显示出良好的吸收和降血脂活性。当喹唑啉酮环系统在6和7位被甲氧基取代时,观察到降血脂活性增加。