氯维甲酸
交易激励
氯贝特酸
查尔酮
化学
代谢物
二苯甲酮
过氧化物酶体增殖物激活受体
药理学
活性代谢物
生物化学
受体
立体化学
有机化学
生物
转录因子
基因
作者
Letizia Giampietro,Alessandra D’Angelo,Antonella Giancristofaro,Alessandra Ammazzalorso,Barbara De Filippis,Mauro DiMatteo,Marialuigia Fantacuzzi,Pasquale Linciano,Cristina Maccallini,Rosa Amoroso
出处
期刊:Medicinal Chemistry
[Bentham Science Publishers]
日期:2013-12-31
卷期号:10 (1): 59-65
被引量:19
标识
DOI:10.2174/157340641001131226123613
摘要
In an effort to develop safe and efficacious compounds for the treatment of metabolic disorders, new compounds based on a combination of clofibric acid, the active metabolite of clofibrate, and trans-stilbene, chalcone, and other lipophilic groups were synthesized. They were evaluated for PPARα transactivation activity; all branched derivatives showed an increase of the transcriptional activity of receptor compared to the linear ones. Noteworthy, stilbene and benzophenone branched derivatives activated the PPARα better than clofibric acid. Keywords: PPARs, clofibrate, chalcone, stilbene, transactivation assay.
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