| Literature DB >> 28327307 |
Daniel E Jeffries1, Jonathan O Witt1, Andrea L McCollum1, Kayla J Temple2, Miguel A Hurtado3, Joel M Harp4, Anna L Blobaum2, Craig W Lindsley5, Corey R Hopkins6.
Abstract
Herein, we report the synthesis and structure-activity relationship of a novel series of (R)-4,4-difluoropiperidine core scaffold as dopamine receptor 4 (D4) antagonists. A series of compounds from this scaffold are highly potent against the D4 receptor and selective against the other dopamine receptors. In addition, we were able to confirm the active isomer as the (R)-enantiomer via an X-ray crystal structure.Entities:
Keywords: Addiction; Difluoropiperidine; Dopamine 4 receptor; PD-LIDs; Selectivity
Mesh:
Substances:
Year: 2016 PMID: 28327307 DOI: 10.1016/j.bmcl.2016.10.049
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823