Non-peptide NK(1) receptor ligands based on the 4-phenylpyridine moiety

Autor: Giuliani G. 1, Cappelli A. 1, Matarrese M. 2, 3, Masiello V. 2, Turolla E.A. 2, Monterisi C. 2, Fazio F. 3, Anzini M. 1, Pericot Mohr G.L. 1, Riitano D. 3, Finetti F. 4, Morbidelli L. 4, Ziche M. 4, Giorgi G. 5, Vomero S. 1

Publikováno v: Bioorganic & medicinal chemistry
19 (2011): 2242–2251.
info:cnr-pdr/source/autori:Giuliani G. 1, Cappelli A. 1, Matarrese M. 2,3, Masiello V. 2,3, Turolla E.A. 2,3, Monterisi C. 2,3, Fazio F. 3, Anzini M. 1, Pericot Mohr G.L. 1, Riitano D. 3, Finetti F. 4, Morbidelli L. 4, Ziche M. 4, Giorgi G. 5, Vomero S. 1/titolo:Non-peptide NK(1) receptor ligands based on the 4-phenylpyridine moiety./doi:/rivista:Bioorganic & medicinal chemistry (Print)/anno:2011/pagina_da:2242/pagina_a:2251/intervallo_pagine:2242–2251/volume:19

The quinoline nucleus of the previously described 4-phenylquinoline-3-carboxamides NK(1) receptor ligands 7 has been transformed into either substituted or azole-(i.e., triazole or tetrazole) fused pyridine moieties of compounds 9 and 10, respectivel

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https://publications.cnr.it/doc/10528