Wang_2000_Bioorg.Med.Chem.Lett_10_2247

Reference

Title : Design and synthesis of piperidinyl piperidine analogues as potent and selective M2 muscarinic receptor antagonists - Wang_2000_Bioorg.Med.Chem.Lett_10_2247
Author(s) : Wang Y , Chackalamannil S , Hu Z , Clader JW , Greenlee W , Billard W , Binch H , Crosby G , Ruperto V , Duffy RA , McQuade R , Lachowicz JE
Ref : Bioorganic & Medicinal Chemistry Lett , 10 :2247 , 2000
Abstract :

Identification of a number of highly potent M2 receptor antagonists with >100-fold selectivity against the M1 and M3 receptor subtypes is described. In the rat microdialysis assay, this series of compounds showed pronounced enhancement of brain acetylcholine release after oral administration.

PubMedSearch : Wang_2000_Bioorg.Med.Chem.Lett_10_2247
PubMedID: 11055330

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Citations formats

Wang Y, Chackalamannil S, Hu Z, Clader JW, Greenlee W, Billard W, Binch H, Crosby G, Ruperto V, Duffy RA, McQuade R, Lachowicz JE (2000)
Design and synthesis of piperidinyl piperidine analogues as potent and selective M2 muscarinic receptor antagonists
Bioorganic & Medicinal Chemistry Lett 10 :2247

Wang Y, Chackalamannil S, Hu Z, Clader JW, Greenlee W, Billard W, Binch H, Crosby G, Ruperto V, Duffy RA, McQuade R, Lachowicz JE (2000)
Bioorganic & Medicinal Chemistry Lett 10 :2247