Rikimaru, Kentaro <br/><br/>
Structure-activity relationships and key structural feature of pyridyloxybenzene-acylsulfonamides as new, potent, and selective peroxisome proliferator-activated receptor (PPAR) γ Agonists.  [electronic resource] 

 -  Bioorganic & medicinal chemistry  May 2012 
 - 3332-58 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S. 
<br/><br/><label>ISSN: </label>1464-3391 
<br/><br/><label>Standard No.: </label>10.1016/j.bmc.2012.03.036  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acylation<br/>Animals<br/>Binding Sites<br/>Blood Glucose--drug effects<br/>CHO Cells<br/>COS Cells<br/>Chlorocebus aethiops<br/>Cricetinae<br/>Crystallography, X-Ray<br/>Drug Design<br/>Humans<br/>Hypoglycemic Agents--chemistry<br/>Male<br/>Models, Molecular<br/>Peroxisome Proliferator-Activated Receptors--agonists<br/>Protein Binding--drug effects<br/>Pyridines--administration & dosage<br/>Rats, Wistar<br/>Structure-Activity Relationship<br/>Sulfonamides--chemistry