Literature DB >> 17191882

Screening of non-alkaloidal natural compounds as acetylcholinesterase inhibitors.

Corinne Brühlmann1, Andrew Marston, Kurt Hostettmann, Pierre-Alain Carrupt, Bernard Testa.   

Abstract

Acetylcholinesterase (AChE) inhibitors are currently the only approved therapy for the treatment of Alzheimer's disease, only a limited number of drugs are commercially available. A library of non-alkaloidal natural compounds was investigated. To this end, a convenient microtitre plate method for assaying AChE inhibition, which allows a complete kinetic analysis of AChE inhibitors, was developed. Seven active compounds with Ki values in the micromolar range were identified, six of which were xanthones. This is the first report that a promising potential for AChE inhibition exists in such non-nitrogenous natural compounds. Furthermore, four xanthones among these xanthones had already been described as monoamine oxidase (MAO) inhibitors, making then dual AChE/MAO inhibitors of great interest.

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Year:  2004        PMID: 17191882     DOI: 10.1002/cbdv.200490064

Source DB:  PubMed          Journal:  Chem Biodivers        ISSN: 1612-1872            Impact factor:   2.408


  6 in total

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Review 2.  Research Advances and Detection Methodologies for Microbe-Derived Acetylcholinesterase Inhibitors: A Systemic Review.

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6.  New 3-O-substituted xanthone derivatives as promising acetylcholinesterase inhibitors.

Authors:  Zi Han Loh; Huey Chong Kwong; Kok Wai Lam; Soek Sin Teh; Gwendoline Cheng Lian Ee; Ching Kheng Quah; Anthony Siong Hock Ho; Siau Hui Mah
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  6 in total

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