Literature DB >> 11851728

Secretases as targets for drug design in Alzheimer's disease.

J V R B Hendriksen1, H S L M Nottet, H A Smits.   

Abstract

Alzheimer's disease accounts for the majority of dementia in the elderly. Worldwide, approximately 20 million people are suffering from this devastating disease, with no effective treatment currently available. For efficient drug design, it is important to identify the molecular mechanisms underlying the pathology of the disease. An invariant feature in the pathology of Alzheimer's disease is the amyloid-beta peptide. Amyloid-beta is produced by endoproteolytic cleavage of the amyloid precursor protein by beta- and gamma-secretase. In the past 2 years, the protein responsible for beta-secretase activity has been isolated and researchers are close to identifying gamma-secretase. These recent achievements in Alzheimer's disease research have provided helpful tools for the development of therapeutics.

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Year:  2002        PMID: 11851728     DOI: 10.1046/j.1365-2362.2002.00937.x

Source DB:  PubMed          Journal:  Eur J Clin Invest        ISSN: 0014-2972            Impact factor:   4.686


  2 in total

1.  Discovery of potent beta-secretase (bace-1) inhibitors by the synthesis of isophthalamide-containing hybrids.

Authors:  Yi-Ping Zhu; Kun Xiao; Hai-Ping Yu; Lan-Ping Ma; Bing Xiong; Hai-Yan Zhang; Xin Wang; Jing-Ya Li; Jia Li; Jing-Kang Shen
Journal:  Acta Pharmacol Sin       Date:  2009-01-26       Impact factor: 6.150

2.  Heparan sulfate regulates amyloid precursor protein processing by BACE1, the Alzheimer's beta-secretase.

Authors:  Zoe Scholefield; Edwin A Yates; Gareth Wayne; Augustin Amour; William McDowell; Jeremy E Turnbull
Journal:  J Cell Biol       Date:  2003-10-06       Impact factor: 10.539

  2 in total

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