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Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors
Integrase (IN) represents a clinically validated target for the development of antivirals against human immunodeficiency virus (HIV). In recent years our research group has been engaged in the stucture-function study of this enzyme and in the development of some three-dimensional pharmacophore model...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264142/ https://www.ncbi.nlm.nih.gov/pubmed/21836543 http://dx.doi.org/10.3390/molecules16086858 |
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author | Ferro, Stefania Grazia, Sara De Luca, Laura De Gitto, Rosaria Faliti, Caterina Elisa Debyzer, Zeger Chimirri, Alba |
author_facet | Ferro, Stefania Grazia, Sara De Luca, Laura De Gitto, Rosaria Faliti, Caterina Elisa Debyzer, Zeger Chimirri, Alba |
author_sort | Ferro, Stefania |
collection | PubMed |
description | Integrase (IN) represents a clinically validated target for the development of antivirals against human immunodeficiency virus (HIV). In recent years our research group has been engaged in the stucture-function study of this enzyme and in the development of some three-dimensional pharmacophore models which have led to the identification of a large series of potent HIV-1 integrase strand-transfer inhibitors (INSTIs) bearing an indole core. To gain a better understanding of the structure-activity relationships (SARs), herein we report the design and microwave-assisted synthesis of a novel series of 1-H-benzylindole derivatives. |
format | Online Article Text |
id | pubmed-6264142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62641422018-12-10 Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors Ferro, Stefania Grazia, Sara De Luca, Laura De Gitto, Rosaria Faliti, Caterina Elisa Debyzer, Zeger Chimirri, Alba Molecules Article Integrase (IN) represents a clinically validated target for the development of antivirals against human immunodeficiency virus (HIV). In recent years our research group has been engaged in the stucture-function study of this enzyme and in the development of some three-dimensional pharmacophore models which have led to the identification of a large series of potent HIV-1 integrase strand-transfer inhibitors (INSTIs) bearing an indole core. To gain a better understanding of the structure-activity relationships (SARs), herein we report the design and microwave-assisted synthesis of a novel series of 1-H-benzylindole derivatives. MDPI 2011-08-11 /pmc/articles/PMC6264142/ /pubmed/21836543 http://dx.doi.org/10.3390/molecules16086858 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Ferro, Stefania Grazia, Sara De Luca, Laura De Gitto, Rosaria Faliti, Caterina Elisa Debyzer, Zeger Chimirri, Alba Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors |
title | Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors |
title_full | Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors |
title_fullStr | Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors |
title_full_unstemmed | Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors |
title_short | Microwave Assisted Organic Synthesis (MAOS) of Small Molecules as Potential HIV-1 Integrase Inhibitors |
title_sort | microwave assisted organic synthesis (maos) of small molecules as potential hiv-1 integrase inhibitors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264142/ https://www.ncbi.nlm.nih.gov/pubmed/21836543 http://dx.doi.org/10.3390/molecules16086858 |
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