Memoquin: A multi-target-directed ligand as an innovative therapeutic opportunity for Alzheimer’s disease

SummaryAlzheimer’s disease is currently thought to be a complex, multifactorial syndrome, unlikely to arise from a single causal factor; instead, a number of related biological alterations are thought to contribute to its pathogenesis. This may explain why the currently available drugs, developed according to the classic drug discovery paradigm of “one-molecule-one-target,” have turned out to be palliative. In light of this, drug combinations that can act at different levels of the neurotoxic cascade offer new avenues toward curing Alzheimer’s and other neurodegenerative diseases. In parallel, a new strategy is emerging—that of developing a single chemical entity able to modulate multiple targets simultaneously. This has led to a new paradigm in medicinal chemistry, the “multi-target-directed ligand” design strategy, which has already been successfully exploited at both academic and industrial levels. As a case study, we report here on memoquin, a new molecule developed following this strategy. The in vitro and in vivo biological profile of memoquin demonstrates the suitability of the new strategy for obtaining innovative drug candidates for the treatment of neurodegenerative diseases.

[1]  Ana Martínez,et al.  Targeting beta-amyloid pathogenesis through acetylcholinesterase inhibitors. , 2006, Current pharmaceutical design.

[2]  Maurizio Recanatini,et al.  Multi-target-directed ligands to combat neurodegenerative diseases. , 2008, Journal of medicinal chemistry.

[3]  J. Hardy,et al.  The Amyloid Hypothesis of Alzheimer ’ s Disease : Progress and Problems on the Road to Therapeutics , 2009 .

[4]  A. Cavalli,et al.  3-(4-[[Benzyl(methyl)amino]methyl]phenyl)-6,7-dimethoxy-2H-2-chromenone (AP2238) inhibits both acetylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation: a dual function lead for Alzheimer's disease therapy. , 2003, Journal of medicinal chemistry.

[5]  N. Inestrosa,et al.  Acetylcholinesterase promotes the aggregation of amyloid-beta-peptide fragments by forming a complex with the growing fibrils. , 1997, Journal of molecular biology.

[6]  A. Cattaneo,et al.  β-Amyloid Plaques in a Model for Sporadic Alzheimer's Disease Based on Transgenic Anti-Nerve Growth Factor Antibodies , 2002, Molecular and Cellular Neuroscience.

[7]  Richard Morphy,et al.  Designed Multiple Ligands. An Emerging Drug Discovery Paradigm , 2006 .

[8]  Claudia Linker,et al.  Acetylcholinesterase Accelerates Assembly of Amyloid-β-Peptides into Alzheimer's Fibrils: Possible Role of the Peripheral Site of the Enzyme , 1996, Neuron.

[9]  M. Recanatini,et al.  Acetylcholinesterase inhibitors as a starting point towards improved Alzheimer's disease therapeutics. , 2004, Current pharmaceutical design.

[10]  A. Olson,et al.  Discovery of acetylcholinesterase peripheral anionic site ligands through computational refinement of a directed library. , 2005, Biochemistry.

[11]  G. Minotti,et al.  Antioxidant properties of 2,3-dimethoxy-5-methyl-6-(10-hydroxydecyl)-1,4-benzoquinone (idebenone). , 1998, Chemical research in toxicology.

[12]  K. Ono,et al.  Preformed beta-amyloid fibrils are destabilized by coenzyme Q10 in vitro. , 2005, Biochemical and biophysical research communications.

[13]  Kathryn Ziegler-Graham,et al.  Forecasting the global burden of Alzheimer’s disease , 2007, Alzheimer's & Dementia.

[14]  Brian J Bacskai,et al.  In vivo optical imaging of amyloid aggregates in brain: design of fluorescent markers. , 2005, Angewandte Chemie.

[15]  S. Brimijoin,et al.  The role of acetylcholinesterase in the pathogenesis of Alzheimer's disease. , 2003, Drugs of today.

[16]  F. Leuven,et al.  Secretases as targets for the treatment of Alzheimer's disease: the prospects , 2002, The Lancet Neurology.

[17]  D. Hadler,et al.  Sustained efficacy and safety of idebenone in the treatment of Alzheimer's disease: update on a 2-year double-blind multicentre study. , 1998, Journal of neural transmission. Supplementum.

[18]  Koki Kato,et al.  Idebenone protects hippocampal neurons against amyloid β-peptide-induced neurotoxicity in rat primary cultures , 1998, Naunyn-Schmiedeberg's Archives of Pharmacology.

[19]  M. Farlow Utilizing combination therapy in the treatment of Alzheimer’s disease , 2004, Expert review of neurotherapeutics.

[20]  A. Castro,et al.  Peripheral and dual binding site acetylcholinesterase inhibitors: implications in treatment of Alzheimer's disease. , 2001, Mini reviews in medicinal chemistry.

[21]  D. Small Acetylcholinesterase inhibitors for the treatment of dementia in Alzheimer’s disease: do we need new inhibitors? , 2005, Expert opinion on emerging drugs.

[22]  M. Farlow,et al.  Treatment Options in Alzheimer’s Disease: Maximizing Benefit, Managing Expectations , 2008, Dementia and Geriatric Cognitive Disorders.

[23]  K. Ono,et al.  Preformed β-amyloid fibrils are destabilized by coenzyme Q10 in vitro , 2005 .

[24]  G. Forloni,et al.  Anti‐amyloidogenic activity of tetracyclines: studies in vitro , 2001, FEBS letters.

[25]  A. Cattaneo,et al.  On the Molecular Basis Linking Nerve Growth Factor (NGF) to Alzheimer’s Disease , 2006, Cellular and Molecular Neurobiology.

[26]  Bruno Dubois,et al.  A review of compliance to treatment in Alzheimer's disease: potential benefits of a transdermal patch , 2007, Current medical research and opinion.

[27]  V. Andrisano,et al.  Propidium-based polyamine ligands as potent inhibitors of acetylcholinesterase and acetylcholinesterase-induced amyloid-beta aggregation. , 2005, Journal of medicinal chemistry.

[28]  S. Noble,et al.  Idebenone: A Review of its Use in Mild to Moderate Alzheimer??s Disease , 1998 .

[29]  Maurizio Recanatini,et al.  Novel class of quinone-bearing polyamines as multi-target-directed ligands to combat Alzheimer's disease. , 2007, Journal of medicinal chemistry.

[30]  T. Golde Disease modifying therapy for AD? 1 , 2006, Journal of neurochemistry.

[31]  H. Ladinsky,et al.  Therapeutic potential of CNS-active M2 antagonists: novel structures and pharmacology. , 1993, Life sciences.

[32]  D. Moller,et al.  Discovery of a potent, highly selective, and orally efficacious small-molecule activator of the insulin receptor. , 2000, Journal of medicinal chemistry.

[33]  A. Raina,et al.  Quinone reductase (NQO1), a sensitive redox indicator, is increased in Alzheimer's disease. , 1999, Redox report : communications in free radical research.

[34]  Yun Tang,et al.  Bis-(-)-nor-meptazinols as novel nanomolar cholinesterase inhibitors with high inhibitory potency on amyloid-beta aggregation. , 2008, Journal of medicinal chemistry.

[35]  V. Tumiatti,et al.  From dual binding site acetylcholinesterase inhibitors to multi-target-directed ligands (MTDLs): a step forward in the treatment of Alzheimer's disease. , 2008, Mini reviews in medicinal chemistry.

[36]  P. Camps,et al.  Dimeric and hybrid anti-Alzheimer drug candidates. , 2006, Current medicinal chemistry.

[37]  I. Grundke‐Iqbal,et al.  Alzheimer disease is multifactorial and heterogeneous , 2000, Neurobiology of Aging.

[38]  M. Smith,et al.  Oxidative stress mechanisms and potential therapeutics in Alzheimer disease , 2005, Journal of Neural Transmission.

[39]        Global prevalence of dementia: a Delphi consensus study , 2006 .

[40]  S. Asano,et al.  Inhibition of Amyloid Protein Aggregation and Neurotoxicity by Rifampicin , 1996, The Journal of Biological Chemistry.

[41]  D. Small,et al.  Alzheimer's disease and Aβ toxicity: from top to bottom , 2001, Nature Reviews Neuroscience.

[42]  V. Andrisano,et al.  beta-Amyloid aggregation induced by human acetylcholinesterase: inhibition studies. , 2003, Biochemical pharmacology.

[43]  A. Cavalli,et al.  Insight Into the Kinetic of Amyloid β (1–42) Peptide Self‐Aggregation: Elucidation of Inhibitors’ Mechanism of Action , 2007, Chembiochem : a European journal of chemical biology.

[44]  N. Berardi,et al.  Alzheimer-like neurodegeneration in aged antinerve growth factor transgenic mice , 2000 .

[45]  L. Mucke,et al.  100 Years and Counting: Prospects for Defeating Alzheimer's Disease , 2006, Science.

[46]  A. Azzi Oxidative stress: A dead end or a laboratory hypothesis? , 2007, Biochemical and biophysical research communications.

[47]  P. Moreira,et al.  Alzheimer's disease: a lesson from mitochondrial dysfunction. , 2007, Antioxidants & redox signaling.

[48]  M L Bolognesi,et al.  Acetylcholinesterase noncovalent inhibitors based on a polyamine backbone for potential use against Alzheimer's disease. , 1998, Journal of medicinal chemistry.

[49]  S. Mandel,et al.  Novel multifunctional anti-Alzheimer drugs with various CNS neurotransmitter targets and neuroprotective moieties. , 2007, Current Alzheimer research.

[50]  J. Pezzuto,et al.  Induction of quinone reductase as a primary screen for natural product anticarcinogens. , 2004, Methods in Enzymology.

[51]  N. Inestrosa,et al.  Brain Acetylcholinesterase Promotes Amyloid-β-Peptide Aggregation but Does Not Hydrolyze Amyloid Precursor Protein Peptides , 1998, Neurochemical Research.

[52]  Charles DeCarli,et al.  Regional NAD(P)H:quinone oxidoreductase activity in Alzheimer’s disease , 2004, Neurobiology of Aging.

[53]  I. Melnikova Therapies for Alzheimer's disease , 2007, Nature Reviews Drug Discovery.

[54]  S. Frantz Drug discovery: Playing dirty , 2005, Nature.

[55]  David B Bylund,et al.  Pharmacologic principles for combination therapy. , 2005, Proceedings of the American Thoracic Society.

[56]  F. J. Luque,et al.  Design, synthesis, and biological evaluation of dual binding site acetylcholinesterase inhibitors: new disease-modifying agents for Alzheimer's disease. , 2005, Journal of medicinal chemistry.

[57]  D. Small,et al.  Alzheimer's disease and Abeta toxicity: from top to bottom. , 2001, Nature reviews. Neuroscience.

[58]  Maurizio Recanatini,et al.  A small molecule targeting the multifactorial nature of Alzheimer's disease. , 2007, Angewandte Chemie.

[59]  Hong-yu Zhang,et al.  How to understand the dichotomy of antioxidants. , 2007, Biochemical and biophysical research communications.

[60]  F. J. Luque,et al.  Novel donepezil-based inhibitors of acetyl- and butyrylcholinesterase and acetylcholinesterase-induced beta-amyloid aggregation. , 2008, Journal of medicinal chemistry.

[61]  C. DeCarli,et al.  NAD(P)H:quinone oxidoreductase activity is increased in hippocampal pyramidal neurons of patients with alzheimer’s disease , 2000, Neurobiology of Aging.

[62]  B. P. Doctor,et al.  Stable Complexes Involving Acetylcholinesterase and Amyloid-β Peptide Change the Biochemical Properties of the Enzyme and Increase the Neurotoxicity of Alzheimer’s Fibrils , 1998, The Journal of Neuroscience.

[63]  P Taylor,et al.  Crystal Structure of Mouse Acetylcholinesterase , 1999, The Journal of Biological Chemistry.