A combination of benzoxazole, phenoxyalkyl side chain, and phenoxybutyric acids was identified as a highly potent and selective human peroxisome proliferator-activated receptor alpha (PPARalpha) agonist. The synthesis, structure-activity relationship (SAR) studies, and in vivo activities of the representative compounds are described.
苯并恶唑,苯氧基烷基侧链和苯氧基
丁酸的组合被确定为高度有效和选择性的人类
过氧化物酶体增殖物激活受体α(
PPARalpha)激动剂。描述了代表性化合物的合成,结构-活性关系(
SAR)研究和体内活性。