Antiobesity designed multiple ligands: Synthesis of pyrazole fatty acid amides and evaluation as hypophagic agents
作者:Mario Alvarado、Pilar Goya、Manuel Macías-González、Francisco Javier Pavón、Antonia Serrano、Nadine Jagerovic、Jose Elguero、Angel Gutiérrez-Rodríguez、Santiago García-Granda、Margarita Suardíaz、Fernando Rodríguez de Fonseca
DOI:10.1016/j.bmc.2008.10.023
日期:2008.12
Searching for new antiobesity agents, a new series of fatty acid amide derivatives of 1,5-diarylpyrazole have been synthesized as dual peroxisome proliferator activated receptor alpha (PPARalpha)/cannabinoid receptor ligands. The compounds have been evaluated in vivo and in vitro as PPARalpha activators and as cannabinoids in two tests of the mouse tetrad. In vivo, food intake studies have been performed
为了寻找新的减肥药,已经合成了一系列新的1,5-二芳基吡唑脂肪酸酰胺衍生物,作为双重过氧化物酶体增殖物激活受体α(PPARalpha)/大麻素受体配体。在小鼠四联体的两次测试中,已将这些化合物作为PPARalpha激活剂和大麻素在体内和体外进行了评估。在体内,已经对所有化合物进行了食物摄入研究。没有发现明显的大麻素活性,但是一些化合物具有有效的PPARalpha活化剂的作用。几种化合物显示出厌食特性,从而减少了大鼠的食物摄入。