Bohme_2001_Bioorg.Med.Chem.Lett_11_1241

Reference

Title : Design and pharmacology of quinuclidine derivatives as M2-selective muscarinic receptor ligands - Bohme_2001_Bioorg.Med.Chem.Lett_11_1241
Author(s) : Bohme TM , Keim C , Dannhardt G , Mutschler E , Lambrecht G
Ref : Bioorganic & Medicinal Chemistry Lett , 11 :1241 , 2001
Abstract :

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.

PubMedSearch : Bohme_2001_Bioorg.Med.Chem.Lett_11_1241
PubMedID: 11354386

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Citations formats

Bohme TM, Keim C, Dannhardt G, Mutschler E, Lambrecht G (2001)
Design and pharmacology of quinuclidine derivatives as M2-selective muscarinic receptor ligands
Bioorganic & Medicinal Chemistry Lett 11 :1241

Bohme TM, Keim C, Dannhardt G, Mutschler E, Lambrecht G (2001)
Bioorganic & Medicinal Chemistry Lett 11 :1241