Skip to search formSkip to main contentSkip to account menu

tesaglitazar

Known as: (2S)-2-Ethoxy-3-(4-(2-(4-((methylsulfonyl)oxy)phenyl)ethoxy)phenyl)propanoic acid, 2-ethoxy-3-(4-((4-(methylsulfonyloxy)phenethyl)oxy)phenyl)propanoic acid, (S)-2-ethoxy-3-(4-(2-(4-methylsulphonyloxyphenyl)ethoxy)phenyl)propanoic acid 
A dual peroxisome proliferator-activated receptor (PPAR) agonist, with hypoglycemic activity. Tesaglitazar is more potent on the gamma subtype than… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT Tesaglitazar, is predominantly metabolized (to an acyl glucuronide of the parent… 
Highly Cited
2007
Highly Cited
2007
Peroxisome proliferator–activated receptors (PPARs) are nuclear transcription factors and play a central role in insulin… 
2007
2007
This randomised, double-blind, parallel-group, mul-ticentre study investigated the effects of the dual peroxisome proliferator… 
2007
2007
The development of the dual peroxisome proliferator-activated receptor (PPAR) alpha/gamma agonist tesaglitazar as an oral… 
2007
2007
This study assessed the effects of tesaglitazar (0.5 or 1 mg/day), a dual peroxisome proliferator-activated receptor α/γ agonist… 
2007
2007
161 The development of glucose intolerance and type 2 diabetes is typically associated with multiple disturbances of endocrine… 
2006
2006
Objective—We investigated whether the dual PPAR&agr;/&ggr; agonist tesaglitazar has anti-atherogenic effects in ApoE*3Leiden mice… 
Review
2006
Review
2006
While glycemic control remains the cornerstone of clinical management for patients with type 2 diabetes, the importance of a more… 
2005
2005
Insulin resistance, impaired glucose tolerance, high circulating levels of free fatty acids (FFA), and postprandial… 
2004