Multi-target-directed ligands to combat neurodegenerative diseases

A Cavalli, ML Bolognesi, A Minarini… - Journal of medicinal …, 2008 - ACS Publications
Our understanding of the pathogenesis of diseases has advanced enormously in recent
decades. As a consequence, drug discovery has gradually shifted from an entirely …

Privileged scaffolds as MAO inhibitors: Retrospect and prospects

AC Tripathi, S Upadhyay, S Paliwal, SK Saraf - European Journal of …, 2018 - Elsevier
This review aims to be a comprehensive, authoritative, critical, and readable review of
general interest to the medicinal chemistry community because it focuses on the …

Emerging therapeutic potentials of dual‐acting MAO and AChE inhibitors in Alzheimer's and Parkinson's diseases

B Mathew, DGT Parambi, GE Mathew… - Archiv der …, 2019 - Wiley Online Library
No drug has been approved to prevent neuronal cell loss in patients suffering from
Parkinson's disease (PD) or Alzheimer's disease (AD); despite increased comprehension of …

Multi-target-directed ligands and other therapeutic strategies in the search of a real solution for Alzheimer's disease

A Agis-Torres, M Sollhuber… - Current …, 2014 - ingentaconnect.com
The lack of an adequate therapy for Alzheimer's Disease (AD) contributes greatly to the
continuous growing amount of papers and reviews, reflecting the important efforts made by …

Past, present and future of A2A adenosine receptor antagonists in the therapy of Parkinson's disease

MT Armentero, A Pinna, S Ferré, JL Lanciego… - Pharmacology & …, 2011 - Elsevier
Several selective antagonists for adenosine A2A receptors (A2AR) are currently under
evaluation in clinical trials (phases I to III) to treat Parkinson's disease, and they will probably …

Therapeutic potential of adenosine A2A receptor antagonists in Parkinson's disease

K Xu, E Bastia, M Schwarzschild - Pharmacology & therapeutics, 2005 - Elsevier
In the pursuit of improved treatments for Parkinson's disease (PD), the adenosine A2A
receptor has emerged as an attractive nondopaminergic target. Based on the compelling …

A convenient one-pot synthesis of 2-substituted benzimidazoles

R Trivedi, SK De, RA Gibbs - Journal of Molecular Catalysis A: Chemical, 2006 - Elsevier
A convenient one-pot synthesis of 2-substituted benzimidazoles - ScienceDirect Skip to main
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[图书][B] Strategies for organic drug synthesis and design

D Lednicer - 2009 - books.google.com
This book examines and evaluates the strategies utilized to design and synthesize
pharmaceutically active agents. Significant updates over the last 10 years since the …

Xanthines as adenosine receptor antagonists

BB Fredholm, CE Müller, KA Jacobson - Methylxanthines, 2011 - Springer
The natural plant alkaloids caffeine and theophylline were the first adenosine receptor (AR)
antagonists described in the literature. They exhibit micromolar affinities and are non …

Synthesis, reactivity and biological activity of benzimidazoles

M Alamgir, DSC Black, N Kumar - Bioactive heterocycles III, 2007 - Springer
Benzimidazole is a biologically important scaffold which displays important biological
activities. Recent progress in the synthesis and bioactivity of benzimidazoles is reviewed …