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A non-peptide NK1 receptor agonist showing subpicomolar affinity
Authors:Cappelli Andrea  Giuliani Germano  Pericot Mohr Gl Gal la  Gallelli Andrea  Anzini Maurizio  Vomero Salvatore  Cupello Aroldo  Scarrone Simona  Matarrese Mario  Moresco Rosa Maria  Fazio Ferruccio  Finetti Federica  Morbidelli Lucia  Ziche Marina
Affiliation:Dipartimento Farmaco Chimico Tecnologico and European Research Centre for Drug Discovery and Development, Università degli Studi di Siena, Via A. Moro, 53100 Siena, Italy. cappelli@unisi.it
Abstract:3-Quinolinecarboxamides have been synthesized and evaluated for their binding to the human NK(1) receptor. Several secondary amide derivatives show NK(1) receptor affinity in the picomolar range. The most active compound, hydroxymethylcarboxamide 3h showing an IC(50) value in the subpicomolar range, behaved as an agonist of NK(1) receptor in endothelial cell proliferation, inositol phosphate turnover, and NO-mediated cyclic GMP accumulation, thus proving it to be the first non-peptide NK(1) receptor agonist showing very high potency.
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