| Literature DB >> 25499438 |
James B Thomas1, Angela M Giddings2, Srinivas Olepu2, Robert W Wiethe2, Danni L Harris2, Sanju Narayanan2, Keith R Warner2, Philippe Sarret3, Jean-Michel Longpre3, Scott P Runyon2, Brian P Gilmour2.
Abstract
Compounds acting via the GPCR neurotensin receptor type 2 (NTS2) display analgesic effects in relevant animal models. Using a pharmacophore model based on known NT receptor nonpeptide compounds, we screened commercial databases to identify compounds that might possess activity at NTS2 receptor sites. Modification of our screening hit to include structural features known to be recognized by NTS1 and NTS2, led to the identification of the novel NTS2 selective nonpeptide, N-{[6-chloro-4-(2,6-dimethoxyphenyl)quinazolin-2-yl]carbonyl}-l-leucine (9). This compound is a potent partial agonist in the FLIPR assay with a profile of activity similar to that of the reference NTS2 analgesic nonpeptide levocabastine (5).Entities:
Keywords: FLIPR assay; Levocabastine; NTS2 receptor; Neurotensin; Pain; SR142948a; SR48692
Mesh:
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Year: 2014 PMID: 25499438 PMCID: PMC4296974 DOI: 10.1016/j.bmcl.2014.11.047
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823