317318-65-3Relevant academic research and scientific papers
Synthesis of the PPARβ/δ-selective agonist GW501516 and C4-thiazole-substituted analogs
Pereira, Raquel,Gaudon, Claudine,Iglesias, Beatriz,Germain, Pierre,Gronemeyer, Hinrich,De Lera, Angel R.
, p. 49 - 54 (2007/10/03)
Sequential, position-selective, Pd-catalyzed cross-coupling reactions of 2,4-dibromo-5-hydroxymethylthiazole provided the scaffold for the synthesis of GW501516, the most potent PPARβ/δ agonist yet described, and equally selective analogs at the thiazole-
Medicaments
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, (2008/06/13)
Methods or prevention or treatment of diseases or conditions where inhibition of NO synthase and/or TNF is desirable, the use of PPAR delta activators in such methods and methods for the identification of compounds useful in such treatment.
Activator of PPAR delta
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, (2008/06/13)
Compounds of Formula (I) are disclosed. These compounds include selective activators of human PPAR delta.
