Substituted azole acid derivatives useful as antidiabetic and antiobesity agents and method
   
   

Compounds are provided which have the structure 1 wherein Q is C or N; R.sup.2a, R.sup.2b, R.sup.2c, X.sub.1 to X.sub.7, R.sup.1, R.sup.2, R.sup.3, R.sup.3a, R.sup.4, A, Y, m, and n are as defined herein, which compounds are useful as antidiabetic, hypolipidemic, and antiobesity agents. The present invention further provides a method for treating obesity and dyslipidemia in mammals including humans through simultaneous inhibition of peroxisome proliferator activated receptor-.gamma. (PPAR.gamma.) and stimulation of peroxisome proliferator activated receptor-.alpha. (PPAR.alpha.).

 
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