185679-35-0Relevant academic research and scientific papers
Substituted oxazoles and thiazoles derivatives as hPPARγ and hPPARα activators
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, (2008/06/13)
The present invention discloses compounds of formula (I), and tautomeric forms, pharmaceutically acceptable salts, or solvates thereof. Preferably, the compounds of the invention are dual activators of hPPARγ and hPPAR{acute over (α)}.
The synthesis of GW710936X to support the development of potent PPARγ agonists
Reynolds, Dominic J,Hermitage, Stephen A
, p. 7765 - 7770 (2007/10/03)
(2S)-[(2-Benzoyl-4-hydroxy-phenyl)amino]-3-{4-[2-(5-methyl-2-phenyloxazol-4- yl)ethoxy]phenyl}propanoic acid has been synthesised from N-Cbz-L-tyrosine methyl ester utilising a copper(I) catalysed N-arylation as the key coupling step. The synthetic route
