Literature DB >> 8411006

3-Substituted, 3-(4-pyridinylmethyl)-1,3-dihydro-1-phenyl-2H-indol-2-ones as acetylcholine release enhancers: synthesis and SAR.

W W Wilkerson1, A A Kergaye, S W Tam.   

Abstract

A series of 3-substituted, 3-(4-pyridinylmethyl)-1,3-dihydro-1-phenyl-2H-indol-2-ones was synthesized and found to enhance the stimulus-induced release of neurotransmitter acetylcholine (AcCh), and by doing so, might be useful in treating cognitive disorders where the level of this neurotransmitter may be diminished in the brain, as in Alzheimer's disease. An attempt has been made to correlate the structure of the 3-substitution with the ability of the compounds to enhance the release of AcCh from the striatum region of rat brain preparations.

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Year:  1993        PMID: 8411006     DOI: 10.1021/jm00072a009

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  Palladium-catalyzed asymmetric allylic alkylation of 3-aryloxindoles with allylidene dipivalate: a useful enol pivalate product.

Authors:  Barry M Trost; James T Masters; Aaron C Burns
Journal:  Angew Chem Int Ed Engl       Date:  2013-01-17       Impact factor: 15.336

2.  An anthrone-based Kv7.2/7.3 channel blocker with improved properties for the investigation of psychiatric and neurodegenerative disorders.

Authors:  Jacob D Porter; Oscar Vivas; C David Weaver; Abdulmohsen Alsafran; Elliot DiMilo; Leggy A Arnold; Eamonn J Dickson; Chris Dockendorff
Journal:  Bioorg Med Chem Lett       Date:  2019-09-14       Impact factor: 2.823

  2 in total

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