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Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster
The cure for Alzheimer's disease (AD) is still unknown. According to Cholinergic hypothesis, Alzheimer's disease is caused by the reduced synthesis of the neurotransmitter, Acetylcholine. Regional cerebral blood flow can be increased in patients with Alzheimer's disease by Acetylcholi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725007/ https://www.ncbi.nlm.nih.gov/pubmed/23904743 http://dx.doi.org/10.6026/97320630009645 |
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author | Hai, Abdul Kizilbash, Nadeem A Zaidi, SyedaHuma H Alruwaili, Jamal |
author_facet | Hai, Abdul Kizilbash, Nadeem A Zaidi, SyedaHuma H Alruwaili, Jamal |
author_sort | Hai, Abdul |
collection | PubMed |
description | The cure for Alzheimer's disease (AD) is still unknown. According to Cholinergic hypothesis, Alzheimer's disease is caused by the reduced synthesis of the neurotransmitter, Acetylcholine. Regional cerebral blood flow can be increased in patients with Alzheimer's disease by Acetylcholinesterase (AChE) inhibitors. In this regard, Tetraphenylporphinesulfonate (TPPS), 5,10,15,20- Tetrakis (4-sulfonatophenyl) porphyrinato Iron(III) Chloride (FeTPPS) and 5,10,15,20-Tetrakis (4-sulfonatophenyl) porphyrinatoIron(III) nitrosyl Chloride (FeNOTPPS) were investigated as candidate compounds for inhibition of Acteylcholinesterase of Drosophila melanogaster (DmAChE) by use of Molecular Docking. The results show that FeNOTPPS forms the most stable complex with DmAChE. |
format | Online Article Text |
id | pubmed-3725007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-37250072013-07-31 Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster Hai, Abdul Kizilbash, Nadeem A Zaidi, SyedaHuma H Alruwaili, Jamal Bioinformation Hypothesis The cure for Alzheimer's disease (AD) is still unknown. According to Cholinergic hypothesis, Alzheimer's disease is caused by the reduced synthesis of the neurotransmitter, Acetylcholine. Regional cerebral blood flow can be increased in patients with Alzheimer's disease by Acetylcholinesterase (AChE) inhibitors. In this regard, Tetraphenylporphinesulfonate (TPPS), 5,10,15,20- Tetrakis (4-sulfonatophenyl) porphyrinato Iron(III) Chloride (FeTPPS) and 5,10,15,20-Tetrakis (4-sulfonatophenyl) porphyrinatoIron(III) nitrosyl Chloride (FeNOTPPS) were investigated as candidate compounds for inhibition of Acteylcholinesterase of Drosophila melanogaster (DmAChE) by use of Molecular Docking. The results show that FeNOTPPS forms the most stable complex with DmAChE. Biomedical Informatics 2013-07-12 /pmc/articles/PMC3725007/ /pubmed/23904743 http://dx.doi.org/10.6026/97320630009645 Text en © 2013 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited. |
spellingShingle | Hypothesis Hai, Abdul Kizilbash, Nadeem A Zaidi, SyedaHuma H Alruwaili, Jamal Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster |
title | Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster |
title_full | Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster |
title_fullStr | Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster |
title_full_unstemmed | Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster |
title_short | Porphyrin derivatives as inhibitors for acetylcholinesterase from Drosophila melanogaster |
title_sort | porphyrin derivatives as inhibitors for acetylcholinesterase from drosophila melanogaster |
topic | Hypothesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725007/ https://www.ncbi.nlm.nih.gov/pubmed/23904743 http://dx.doi.org/10.6026/97320630009645 |
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