4.7 Article

N-Acylaminophenothiazines: Neuroprotective agents displaying multifunctional activities for a potential treatment of Alzheimer's disease

Journal

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 46, Issue 6, Pages 2224-2235

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2011.03.003

Keywords

N-Acylaminophenothiazines; Butyrylcholinesterase inhibition; Neuroprotection; Oxidative stress; Okadaic acid; Beta-amyloid peptide; Calcium modulation; Alzheimer's disease

Funding

  1. Spanish Ministry of Science and Innovation MICINN [SAF2006-01249, SAF2009-13015-C02-01, SAF2009-12150]
  2. Community of Madrid [S-SAL/0275/2006]
  3. Institute of Health Carlos III (Red RENEVAS) [RETICS-RD06/0026]
  4. CSIC
  5. MICINN
  6. Fundacion Teofilo Hernando, Universidad Autonoma de Madrid, Spain

Ask authors/readers for more resources

We have previously reported the multifunctional profile of N-(3-chloro-10H-phenothiazin-10-yl)-3-(dimethylamino)propanamide (1) as an effective neuroprotectant and selective butyrylcholinesterase inhibitor. In this paper, we have developed a series of N-acylaminophenothiazines obtained from our compound library or newly synthesised. At micro- and sub-micromolar concentrations, these compounds selectively inhibited butyrylcholinesterase (BuChE), protected neurons against damage caused by both exogenous and mitochondrial free radicals, showed low toxicity, and could penetrate into the CNS. In addition, N-(3-chloro-10H-phenothiazin-10-yl)-2-(pyrrolidin-1-yl)acetamide (11) modulated the cytosolic calcium concentration and protected human neuroblastoma cells against several toxics, such as calcium overload induced by an L-type Ca2+-channel agonist, tau-hyperphosphorylation induced by okadaic acid and A beta peptide. (C) 2011 Elsevier Masson SAS. All rights reserved.

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