Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder with few therapeutic options. While several gene mutations have been implicated in ALS, the exact cause of neuronal dysfunction is unknown and motor neurons of affected individuals display numerous cellular abnormalities. Ongo...

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Main Authors: Allison S. Limpert, Margrith E. Mattmann, Nicholas D. P. Cosford
Format: Article
Language:English
Published: Beilstein-Institut 2013-04-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.9.82
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spelling doaj-d18a76b00dbf429ba172335302c370af2021-02-02T03:13:06ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972013-04-019171773210.3762/bjoc.9.821860-5397-9-82Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)Allison S. Limpert0Margrith E. Mattmann1Nicholas D. P. Cosford2Apoptosis and Cell Death Research Program, Sanford-Burnham Medical Research Institute, 10901 N. Torrey Pines Road, La Jolla, California 92037, United StatesApoptosis and Cell Death Research Program, Sanford-Burnham Medical Research Institute, 10901 N. Torrey Pines Road, La Jolla, California 92037, United StatesApoptosis and Cell Death Research Program, Sanford-Burnham Medical Research Institute, 10901 N. Torrey Pines Road, La Jolla, California 92037, United StatesAmyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder with few therapeutic options. While several gene mutations have been implicated in ALS, the exact cause of neuronal dysfunction is unknown and motor neurons of affected individuals display numerous cellular abnormalities. Ongoing efforts to develop novel ALS treatments involve the identification of small molecules targeting specific mechanisms of neuronal pathology, including glutamate excitotoxicity, mutant protein aggregation, endoplasmic reticulum (ER) stress, loss of trophic factors, oxidative stress, or neuroinflammation. Herein, we review recent advances in the discovery and preclinical characterization of lead compounds that may ultimately provide novel drugs to treat patients suffering from ALS.https://doi.org/10.3762/bjoc.9.82amyotrophic lateral sclerosis (ALS)copper/zinc (Cu-Zn) superoxide dismutase 1 (SOD1)glutamate toxicityneurodegenerationoxidative stress
collection DOAJ
language English
format Article
sources DOAJ
author Allison S. Limpert
Margrith E. Mattmann
Nicholas D. P. Cosford
spellingShingle Allison S. Limpert
Margrith E. Mattmann
Nicholas D. P. Cosford
Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)
Beilstein Journal of Organic Chemistry
amyotrophic lateral sclerosis (ALS)
copper/zinc (Cu-Zn) superoxide dismutase 1 (SOD1)
glutamate toxicity
neurodegeneration
oxidative stress
author_facet Allison S. Limpert
Margrith E. Mattmann
Nicholas D. P. Cosford
author_sort Allison S. Limpert
title Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)
title_short Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)
title_full Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)
title_fullStr Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)
title_full_unstemmed Recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (ALS)
title_sort recent progress in the discovery of small molecules for the treatment of amyotrophic lateral sclerosis (als)
publisher Beilstein-Institut
series Beilstein Journal of Organic Chemistry
issn 1860-5397
publishDate 2013-04-01
description Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder with few therapeutic options. While several gene mutations have been implicated in ALS, the exact cause of neuronal dysfunction is unknown and motor neurons of affected individuals display numerous cellular abnormalities. Ongoing efforts to develop novel ALS treatments involve the identification of small molecules targeting specific mechanisms of neuronal pathology, including glutamate excitotoxicity, mutant protein aggregation, endoplasmic reticulum (ER) stress, loss of trophic factors, oxidative stress, or neuroinflammation. Herein, we review recent advances in the discovery and preclinical characterization of lead compounds that may ultimately provide novel drugs to treat patients suffering from ALS.
topic amyotrophic lateral sclerosis (ALS)
copper/zinc (Cu-Zn) superoxide dismutase 1 (SOD1)
glutamate toxicity
neurodegeneration
oxidative stress
url https://doi.org/10.3762/bjoc.9.82
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