Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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
_version_ 1784867164500525056
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
work_keys_str_mv AT dimiccosimone identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT terraccianostefania identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT pierrimartina identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT cantonevincenza identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT lieningstefanie identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT konigstefanie identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT garschaulrike identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT hofstetterrobertklaus identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT koeberleandreas identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT werzoliver identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT brunoines identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors
AT bifulcogiuseppe identificationof24dinitrobiphenylbasedcompoundsasmapeginhibitors