| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1369972 | Bioorganic & Medicinal Chemistry Letters | 2012 | 5 Pages |
Abstract
A series of substituted 4-arylpiperidines and a smaller family of 4-aryl-1,2,3,6-tetrahydropyridines were synthesized and their biological activity at the 5-HT2C receptor studied to determine whether either series showed noteworthy agonist activity. Structure–activity relationships were developed from the performed receptor binding assays and functional studies, and the results of the analysis are presented herein.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Richard J. Conway, Celine Valant, Arthur Christopoulos, Alan D. Robertson, Ben Capuano, Ian T. Crosby,