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Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products
Over-regulation of Heme oxygenase 1 (HO-1) has been recently identified in many types of human cancer, and in these cases, poor clinical outcomes are normally reported. Indeed, the inhibition of HO-1 is being considered as an anticancer approach. Imidazole scaffold is normally present in most of the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409521/ https://www.ncbi.nlm.nih.gov/pubmed/30759842 http://dx.doi.org/10.3390/md17020113 |
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author | Floresta, Giuseppe Amata, Emanuele Gentile, Davide Romeo, Giuseppe Marrazzo, Agostino Pittalà, Valeria Salerno, Loredana Rescifina, Antonio |
author_facet | Floresta, Giuseppe Amata, Emanuele Gentile, Davide Romeo, Giuseppe Marrazzo, Agostino Pittalà, Valeria Salerno, Loredana Rescifina, Antonio |
author_sort | Floresta, Giuseppe |
collection | PubMed |
description | Over-regulation of Heme oxygenase 1 (HO-1) has been recently identified in many types of human cancer, and in these cases, poor clinical outcomes are normally reported. Indeed, the inhibition of HO-1 is being considered as an anticancer approach. Imidazole scaffold is normally present in most of the classical HO-1 inhibitors and seems indispensable to the inhibitory activity due to its strong interaction with the Fe(II) of the heme group. In this paper, we searched for new potentially HO-1 inhibitors among three different databases: Marine Natural Products (MNP), ZINC Natural Products (ZNP) and Super Natural II (SN2). 484,527 compounds were retrieved from the databases and filtered through four statistical/computational filters (2D descriptors, 2D-QSAR pharmacophoric model, 3D-QSAR pharmacophoric model, and docking). Different imidazole-based compounds were suggested by our methodology to be potentially active in inhibiting the HO-1, and the results have been rationalized by the bioactivity of the filtered molecules reported in the literature. |
format | Online Article Text |
id | pubmed-6409521 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64095212019-03-29 Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products Floresta, Giuseppe Amata, Emanuele Gentile, Davide Romeo, Giuseppe Marrazzo, Agostino Pittalà, Valeria Salerno, Loredana Rescifina, Antonio Mar Drugs Article Over-regulation of Heme oxygenase 1 (HO-1) has been recently identified in many types of human cancer, and in these cases, poor clinical outcomes are normally reported. Indeed, the inhibition of HO-1 is being considered as an anticancer approach. Imidazole scaffold is normally present in most of the classical HO-1 inhibitors and seems indispensable to the inhibitory activity due to its strong interaction with the Fe(II) of the heme group. In this paper, we searched for new potentially HO-1 inhibitors among three different databases: Marine Natural Products (MNP), ZINC Natural Products (ZNP) and Super Natural II (SN2). 484,527 compounds were retrieved from the databases and filtered through four statistical/computational filters (2D descriptors, 2D-QSAR pharmacophoric model, 3D-QSAR pharmacophoric model, and docking). Different imidazole-based compounds were suggested by our methodology to be potentially active in inhibiting the HO-1, and the results have been rationalized by the bioactivity of the filtered molecules reported in the literature. MDPI 2019-02-12 /pmc/articles/PMC6409521/ /pubmed/30759842 http://dx.doi.org/10.3390/md17020113 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Floresta, Giuseppe Amata, Emanuele Gentile, Davide Romeo, Giuseppe Marrazzo, Agostino Pittalà, Valeria Salerno, Loredana Rescifina, Antonio Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products |
title | Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products |
title_full | Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products |
title_fullStr | Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products |
title_full_unstemmed | Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products |
title_short | Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products |
title_sort | fourfold filtered statistical/computational approach for the identification of imidazole compounds as ho-1 inhibitors from natural products |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409521/ https://www.ncbi.nlm.nih.gov/pubmed/30759842 http://dx.doi.org/10.3390/md17020113 |
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