Engler, Thomas A <br/><br/>
Substituted 3-imidazo[1,2-a]pyridin-3-yl- 4-(1,2,3,4-tetrahydro-[1,4]diazepino-[6,7,1-hi]indol-7-yl)pyrrole-2,5-diones as highly selective and potent inhibitors of glycogen synthase kinase-3.  [electronic resource] 

 -  Journal of medicinal chemistry  Jul 2004 
 - 3934-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-2623 
<br/><br/><label>Standard No.: </label>10.1021/jm049768a  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Administration, Oral<br/>Animals<br/>Diabetes Mellitus, Type 2--drug therapy<br/>Female<br/>Glycogen Synthase Kinase 3--antagonists & inhibitors<br/>Glycogen Synthase Kinase 3 beta<br/>Humans<br/>Imidazoles--chemical synthesis<br/>Pyridines--chemical synthesis<br/>Pyrroles--chemical synthesis<br/>Rats<br/>Rats, Zucker