过氧化物酶体增殖物激活受体
过氧化物酶体
PPAR激动剂
受体
药理学
化学
非酒精性脂肪肝
医学
生物信息学
计算生物学
脂肪肝
生物
疾病
内科学
作者
Barbara De Filippis,Arianna Granese,Alessandra Ammazzalorso
标识
DOI:10.1080/13543776.2024.2332661
摘要
The search for novel compounds targeting Peroxisome Proliferator-Activated Receptors (PPARs) is currently ongoing, starting from the previous successfully identification of selective, dual or pan agonists. In last years, researchers' efforts are mainly paid to the discovery of PPARγ and δ modulators, both agonists and antagonists, selective or with a dual-multitarget profile. Some of these compounds are currently under clinical trials for the treatment of primary biliary cirrhosis, nonalcoholic fatty liver disease, hepatic, and renal diseases.
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