Journal
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 121, Issue -, Pages 803-809Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2015.07.028
Keywords
Alzheimer's disease; Amyloid beta peptide; Aggregation; Thiosemicarbazone; Fluorescence; Cytotoxicity
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Funding
- Department of Biotechnology, India [BT/Bio CARe/03/656/2010-11, BT/PR3871/MED/30/830/2012]
- UGC
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Aggregation of amyloid 3 peptide (A beta) is an important event in the progression of Alzheimer's disease. Therefore, among the available therapeutic approaches to fight with disease, inhibition of AP aggregation is widely studied and one of the promising approach for the development of treatments for Alzheimer's disease. Thiosemicarbazone compounds are known for their variety of biological activities. However, the potential of thiosemicarbazone compounds towards inhibition of A beta peptide aggregation and the subsequent toxicity is little explored. Herein, we report synthesis and x-ray crystal structure of novel compound 3-acetyl coumarin thiosemicarbazone and its efficacy toward inhibition of A beta(1-42) peptide aggregation. Our results indicate that 3-acetyl coumarin thiosemicarbazone inhibits A beta(1-42) peptide aggregation up to 80% compared to the parent 3-acetyl coumarin which inhibits 52%. Further, 3-acetyl coumarin thiosemicarbazone provides neuroprotection against A beta-induced cytotoxicity in SH-SY5Y cell line. These findings indicate that thiosemicarbazone modification renders 3-acetyl coumarin neuroprotective properties. (C) 2015 Elsevier Masson SAS. All rights reserved.
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