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Docking Studies and Biological Activity of Fosinopril Analogs
The purpose of the present study was to determine the angiotensin-I converting enzyme inhibitory activity of few novel Fosinopril derivatives which were predicted to possess better ACE inhibitory activity and lesser side effects than the existing drug molecule. In vitro study was carried out to dete...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207403/ https://www.ncbi.nlm.nih.gov/pubmed/25383221 http://dx.doi.org/10.1155/2014/721834 |
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author | Choudary, Jayant Kini, Suvarna G. Ranganath Pai Karkala, Sreedhara Mubeen, Muhammad |
author_facet | Choudary, Jayant Kini, Suvarna G. Ranganath Pai Karkala, Sreedhara Mubeen, Muhammad |
author_sort | Choudary, Jayant |
collection | PubMed |
description | The purpose of the present study was to determine the angiotensin-I converting enzyme inhibitory activity of few novel Fosinopril derivatives which were predicted to possess better ACE inhibitory activity and lesser side effects than the existing drug molecule. In vitro study was carried out to determine ACE inhibitory activity of six different Fosinopril analogs by spectrophotometric assay procedure. Analog A2 showed the highest activity compared to other analogs and as well as Fosinopril itself. Docking studies of the compounds were done with the help of VLife MDS 3.0 software using GRIP batch docking method to find out which derivative had a better docking with ACE. The compounds which showed the highest negative score in docking have also exhibited good ACE inhibitory activity. |
format | Online Article Text |
id | pubmed-4207403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42074032014-11-09 Docking Studies and Biological Activity of Fosinopril Analogs Choudary, Jayant Kini, Suvarna G. Ranganath Pai Karkala, Sreedhara Mubeen, Muhammad Int J Med Chem Research Article The purpose of the present study was to determine the angiotensin-I converting enzyme inhibitory activity of few novel Fosinopril derivatives which were predicted to possess better ACE inhibitory activity and lesser side effects than the existing drug molecule. In vitro study was carried out to determine ACE inhibitory activity of six different Fosinopril analogs by spectrophotometric assay procedure. Analog A2 showed the highest activity compared to other analogs and as well as Fosinopril itself. Docking studies of the compounds were done with the help of VLife MDS 3.0 software using GRIP batch docking method to find out which derivative had a better docking with ACE. The compounds which showed the highest negative score in docking have also exhibited good ACE inhibitory activity. Hindawi Publishing Corporation 2014 2014-07-06 /pmc/articles/PMC4207403/ /pubmed/25383221 http://dx.doi.org/10.1155/2014/721834 Text en Copyright © 2014 Jayant Choudary et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Choudary, Jayant Kini, Suvarna G. Ranganath Pai Karkala, Sreedhara Mubeen, Muhammad Docking Studies and Biological Activity of Fosinopril Analogs |
title | Docking Studies and Biological Activity of Fosinopril Analogs |
title_full | Docking Studies and Biological Activity of Fosinopril Analogs |
title_fullStr | Docking Studies and Biological Activity of Fosinopril Analogs |
title_full_unstemmed | Docking Studies and Biological Activity of Fosinopril Analogs |
title_short | Docking Studies and Biological Activity of Fosinopril Analogs |
title_sort | docking studies and biological activity of fosinopril analogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207403/ https://www.ncbi.nlm.nih.gov/pubmed/25383221 http://dx.doi.org/10.1155/2014/721834 |
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