Journal
CHEMMEDCHEM
Volume 1, Issue 2, Pages 256-266Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cmdc.200500039
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Funding
- NIMH NIH HHS [R01 MH079400] Funding Source: Medline
- NINDS NIH HHS [NS-45326, NS-34914] Funding Source: Medline
- PHS HHS [2-494543-440000-1911] Funding Source: Medline
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Research by Klein and co-workers suggests that the inhibition of GSK-3 beta by small molecules may offer an important strategy in the treatment of a number of central nervous system (CNS) disorders including Alzheimer's disease, Parkinson's disease, and bipolar disorders. Based on results from kinase-screening assays that identified a staurosporine analogue as a modest inhibitor of GSK-3 beta, a series of 3-indolyl-4-indazolylmaleimides was prepared for study in both enzymatic and cell-based assays. Most strikingly, whereas we identified ligands having poor to high potency for GSK-3 beta inhibition, only ligands with a K-i value of less than 8 nm, namely maleimides 18 and 22, were found to inhibit Tau phosphorylation at a GSK-3 beta-specific site (Ser396/404). Accordingly, maleimides 18 and 22 may protect neuronal cells against cell death by decreasing the level of alpha-Syn protein expression. We conclude that the GSK-3 beta inhibitors described herein offer promise in defending cells against MPP+-induced neurotoxicity and that such compounds will be valuable to explore in animal models of Parkinson's disease as well as in other Tau-related neurodegenerative disease states.
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