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J Med Chem ; 48(7): 2262-5, 2005 Apr 07.
Article in English | MEDLINE | ID: mdl-15801817

ABSTRACT

A series of 2-aryloxy-2-methyl-propionic acid compounds and related analogues were designed, synthesized, and evaluated for their PPAR agonist activities. 2-[(5,7-Dipropyl-3-trifluoromethyl)-benzisoxazol-6-yloxy]-2-methylpropionic acid (4) was identified as a PPARalpha/gamma dual agonist with relative PPARalpha selectivity and demonstrated potent efficacy in lowering both glucose and lipids in animal models without causing body weight gain. The PPARalpha activity of 4 appeared to have played a significant role in lowering glucose levels in db/db mice.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Hyperlipidemias/drug therapy , Hypoglycemic Agents/chemical synthesis , Hypolipidemic Agents/chemical synthesis , Isoxazoles/chemical synthesis , PPAR alpha/agonists , PPAR gamma/agonists , Propionates/chemical synthesis , 3T3-L1 Cells , Animals , Blood Glucose/drug effects , COS Cells , Carrier Proteins/biosynthesis , Carrier Proteins/genetics , Chlorocebus aethiops , Cholesterol/blood , Dogs , Fatty Acid-Binding Proteins , Humans , Hypoglycemic Agents/chemistry , Hypoglycemic Agents/pharmacology , Hypolipidemic Agents/chemistry , Hypolipidemic Agents/pharmacology , Isoxazoles/chemistry , Isoxazoles/pharmacology , Mice , Mice, Obese , Propionates/chemistry , Propionates/pharmacology , RNA, Messenger/biosynthesis , Radioligand Assay , Structure-Activity Relationship , Transcriptional Activation , Triglycerides/blood , Weight Gain
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