Watanabe T, Hayashi K, Yoshimatsu S, Sakai K, Takeyama S, Takashima K
J Med Chem. 1980 Jan;23(1):50-9. doi: 10.1021/jm00175a010.
More than 110 derivatives of alkoxycinnamic acids were synthesized and their hypolipidemic activities were evaluated in a screening system with rats. Cinnamic acids, alpha-methylcinnamic acids, and their various esters with a higher p-alkoxy substituent were found to possess hypolipidemic activities higher than or comparable to that of clofibrate. The proper length (C12--C16) and the para position of the alkoxy substituent seem to be essential for activity. Chloroethyl and methacryloxyethyl esters and monoglycerides of some of the active p-alkoxycinnamic acids were more active than the corresponding free acids.
合成了110多种烷氧基肉桂酸衍生物,并在大鼠筛选系统中评估了它们的降血脂活性。发现肉桂酸、α-甲基肉桂酸及其具有较高对烷氧基取代基的各种酯具有高于或与氯贝丁酯相当的降血脂活性。烷氧基取代基的适当长度(C12 - C16)和对位似乎对活性至关重要。一些活性对烷氧基肉桂酸的氯乙酯、甲基丙烯酸氧乙酯和甘油单酯比相应的游离酸更具活性。