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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...

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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
Descripción
Sumario: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.