Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10594151 | Bioorganic & Medicinal Chemistry Letters | 2011 | 5 Pages |
Abstract
A series of small molecules based on a chemotype identified from our compound collection were synthesized and tested for binding affinity (IC50) at the human Neuropeptide Y Y2 receptor (NPY Y2). Six of the 23 analogs tested possessed an NPY Y2 IC50 ⩽ 15 nM. One member of this series, JNJ 31020028, is a selective, high affinity, receptor antagonist existing as a racemic mixture. As such a synthetic route to the desired enantiomer was designed starting from commercially available (S)-(+)-mandelic acid.
Keywords
K2CO3BOCMSCLHOBtNBSDCCEtOAcAIBNNaHCO3Na2SO4CCl4TFAN-bromosuccinimideDMFDCMNeuropeptide Y Y2 receptorEDCINa2CO3Et3NHClEt2OTHFNaOH1-ethyl-3-(3-dimethylaminopropyl)carbodiimide1-hydroxy-benzotriazoleN,N′-dicyclohexylcarbodiimideEtherEthyl acetateTrifluoroacetic acidbutoxycarbonylTetrahydrofurantriethylaminediisopropylethylaminedimethylformamideDichloromethanesodium bicarbonateSodium sulfateMethanolMeOHDIPEAsodium hydroxidehydrochlorideCarbon tetrachlorideSodium carbonatePotassium CarbonateNeuropeptide Y
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Devin M. Swanson, Victoria D. Wong, Jill A. Jablonowski, Chandra Shah, Dale A. Rudolph, Curt A. Dvorak, Mark Seierstad, Lisa K. Dvorak, Kirsten Morton, Diane Nepomuceno, John R. Atack, Pascal Bonaventure, Timothy W. Lovenberg, Nicholas I. Carruthers,