| Literature DB >> 28745513 |
Zhenjian Lin, Misty D Smith, Gisela P Concepcion1, Margo G Haygood, Baldomero M Olivera, Alan Light, Eric W Schmidt.
Abstract
Serotonin (5-HT) receptors are important in health and disease, but the existence of 14 subtypes necessitates selective ligands. Previously, the pulicatins were identified as ligands that specifically bound to the subtype 5-HT2B in the 500 nM to 10 μM range and that exhibited in vitro effects on cultured mouse neurons. Here, we examined the structure-activity relationship of 30 synthetic and natural pulicatin derivatives using binding, receptor functionality, and in vivo assays. The results reveal the 2-arylthiazoline scaffold as a tunable serotonin receptor-targeting pharmacophore. Tests in mice show potential antiseizure and antinociceptive activities at high doses without motor impairment.Entities:
Mesh:
Substances:
Year: 2017 PMID: 28745513 PMCID: PMC6025773 DOI: 10.1021/acs.jnatprod.7b00317
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050