The invention relates to oxadiazolones and to their physiologically
acceptable salts and physiologically functional derivatives showing
PPARdelta agonist activity.
What is described are compounds of the formula I,
in which the radicals are as defined, and their physiologically acceptable
salts and processes for their preparations. The compounds are suitable
for the treatment and/or prevention of disorders of fatty acid metabolism
and glucose utilization disorders as well as of disorders in which
insulin resistance is involved; neurodegenerative diseases and/or
de-myelinating disorders of the central and peripheral nervous systems
and/or neurological diseases involving neuro-inflammatory processes
and/or other peripheral neuropathies.