Mortell_2010_Bioorg.Med.Chem.Lett_20_104

Reference

Title : Structure-activity relationships of N-substituted ligands for the alpha7 nicotinic acetylcholine receptor - Mortell_2010_Bioorg.Med.Chem.Lett_20_104
Author(s) : Mortell KH , Schrimpf MR , Bunnelle WH , Anderson DJ , Gronlien JH , Hagene KT , Gopalakrishnan M
Ref : Bioorganic & Medicinal Chemistry Lett , 20 :104 , 2010
Abstract :

A series of alpha7 neuronal nicotinic acetylcholine receptor ligands were designed based on a structural combination of a potent, but non-selective ligand, epibatidine, with a selective lead structure, 2. Three series of compounds in which aryl moieties were attached via a linker to different positions on the core structure were studied. A potent and functionally efficacious analog, (3aR,6aS)-2-(6-phenylpyridazin-3-yl)-5-(pyridin-3-ylmethyl)octahydropyrrolo[3,4-c ]pyrrole (3a), was identified.

PubMedSearch : Mortell_2010_Bioorg.Med.Chem.Lett_20_104
PubMedID: 19954975

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Citations formats

Mortell KH, Schrimpf MR, Bunnelle WH, Anderson DJ, Gronlien JH, Hagene KT, Gopalakrishnan M (2010)
Structure-activity relationships of N-substituted ligands for the alpha7 nicotinic acetylcholine receptor
Bioorganic & Medicinal Chemistry Lett 20 :104

Mortell KH, Schrimpf MR, Bunnelle WH, Anderson DJ, Gronlien JH, Hagene KT, Gopalakrishnan M (2010)
Bioorganic & Medicinal Chemistry Lett 20 :104