1.
Bioorg Med Chem Lett
; 11(9): 1241-3, 2001 May 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-11354386
RESUMO
In our search for M2-selective muscarinic receptor antagonists, we synthesized 1,3-disubstituted indenes. The effects of different basic moieties with regard to binding and selectivity towards the five distinct muscarinic receptor subtypes were investigated. The results show that the quinuclidine series afforded the most promising compounds in terms of both receptor affinity and M2-subtype selectivity.