Structure–activity relationship (SAR) studies on substituted N-(pyridin-3-yl)-2-amino-isonicotinamides as highly potent and selective glycogen synthase kinase-3 (GSK-3) inhibitors

Author:

Luo GuanglinORCID,Chen Ling,Jacutin-Porte Swanee,Han Ying,Burton Catherine R.,Xiao Hong,Krause Carol M.,Cao Yang,Liu Nengyin,Kish Kevin,Lewis Hal A.,Macor John E.,Dubowchik Gene M.ORCID

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference28 articles.

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2. The multifaceted roles of glycogen synthase kinase 3ß in cellular signaling;Grimes;Prog Neurobiol,2001

3. Distribution, levels, and activity of glycogen synthase kinase-3 in the Alzheimer disease brain;Pei;J Neuropathol Exp Neurol,1997

4. Distribution of active glycogen synthase kinase 3beta (GSK-3beta) in brains staged for Alzheimer disease neurofibrillary changes;Pei;J Neuropathol Exp Neurol,1999

5. Functional implications of glycogen synthase kinase-3-mediated Tau phosphorylation;Hanger;Int J Alzheimer’s Dis,2011

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