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Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors
We identified 2,4‐dinitro‐biphenyl‐based compounds as new inhibitors of leukotriene C(4) synthase (LTC(4)S) and 5‐lipoxygenase‐activating protein (FLAP), both members of the “Membrane Associated Proteins in Eicosanoid and Glutathione metabolism” (MAPEG) family involved in the biosynthesis of pro‐inf...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827972/ https://www.ncbi.nlm.nih.gov/pubmed/36111583 http://dx.doi.org/10.1002/cmdc.202200327 |
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author | Di Micco, Simone Terracciano, Stefania Pierri, Martina Cantone, Vincenza Liening, Stefanie König, Stefanie Garscha, Ulrike Hofstetter, Robert Klaus Koeberle, Andreas Werz, Oliver Bruno, Ines Bifulco, Giuseppe |
author_facet | Di Micco, Simone Terracciano, Stefania Pierri, Martina Cantone, Vincenza Liening, Stefanie König, Stefanie Garscha, Ulrike Hofstetter, Robert Klaus Koeberle, Andreas Werz, Oliver Bruno, Ines Bifulco, Giuseppe |
author_sort | Di Micco, Simone |
collection | PubMed |
description | We identified 2,4‐dinitro‐biphenyl‐based compounds as new inhibitors of leukotriene C(4) synthase (LTC(4)S) and 5‐lipoxygenase‐activating protein (FLAP), both members of the “Membrane Associated Proteins in Eicosanoid and Glutathione metabolism” (MAPEG) family involved in the biosynthesis of pro‐inflammatory eicosanoids. By molecular docking we evaluated the putative binding against the targets of interest, and by applying cell‐free and cell‐based assays we assessed the inhibition of LTC(4)S and FLAP by the small molecules at low micromolar concentrations. The present results integrate the previously observed inhibitory profile of the tested compounds against another MAPEG member, i. e., microsomal prostaglandin E(2) synthase (mPGES)‐1, suggesting that the 2,4‐dinitro‐biphenyl scaffold is a suitable molecular platform for a multitargeting approach to modulate pro‐inflammatory mediators in inflammation and cancer treatment. |
format | Online Article Text |
id | pubmed-9827972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98279722023-01-10 Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors Di Micco, Simone Terracciano, Stefania Pierri, Martina Cantone, Vincenza Liening, Stefanie König, Stefanie Garscha, Ulrike Hofstetter, Robert Klaus Koeberle, Andreas Werz, Oliver Bruno, Ines Bifulco, Giuseppe ChemMedChem Research Articles We identified 2,4‐dinitro‐biphenyl‐based compounds as new inhibitors of leukotriene C(4) synthase (LTC(4)S) and 5‐lipoxygenase‐activating protein (FLAP), both members of the “Membrane Associated Proteins in Eicosanoid and Glutathione metabolism” (MAPEG) family involved in the biosynthesis of pro‐inflammatory eicosanoids. By molecular docking we evaluated the putative binding against the targets of interest, and by applying cell‐free and cell‐based assays we assessed the inhibition of LTC(4)S and FLAP by the small molecules at low micromolar concentrations. The present results integrate the previously observed inhibitory profile of the tested compounds against another MAPEG member, i. e., microsomal prostaglandin E(2) synthase (mPGES)‐1, suggesting that the 2,4‐dinitro‐biphenyl scaffold is a suitable molecular platform for a multitargeting approach to modulate pro‐inflammatory mediators in inflammation and cancer treatment. John Wiley and Sons Inc. 2022-10-11 2022-11-18 /pmc/articles/PMC9827972/ /pubmed/36111583 http://dx.doi.org/10.1002/cmdc.202200327 Text en © 2022 The Authors. ChemMedChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Di Micco, Simone Terracciano, Stefania Pierri, Martina Cantone, Vincenza Liening, Stefanie König, Stefanie Garscha, Ulrike Hofstetter, Robert Klaus Koeberle, Andreas Werz, Oliver Bruno, Ines Bifulco, Giuseppe Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors |
title | Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors |
title_full | Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors |
title_fullStr | Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors |
title_full_unstemmed | Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors |
title_short | Identification of 2,4‐Dinitro‐Biphenyl‐Based Compounds as MAPEG Inhibitors |
title_sort | identification of 2,4‐dinitro‐biphenyl‐based compounds as mapeg inhibitors |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827972/ https://www.ncbi.nlm.nih.gov/pubmed/36111583 http://dx.doi.org/10.1002/cmdc.202200327 |
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