1.
Bioorg Med Chem Lett
; 16(13): 3415-8, 2006 Jul 01.
Artículo
en Inglés
| MEDLINE
| ID: mdl-16677814
RESUMEN
The synthesis and biological evaluation of novel tetrahydroisoquinoline, tetrahydroquinoline, and tetrahydroazepine antagonists of the human and rat H(3) receptors are described. The substitution around these rings as well as the nature of the substituent on nitrogen is explored. Several compounds with high affinity and selectivity for the human and rat H(3) receptors are reported.