Multitarget approaches are highly effective strategies for treating acute and chronic inflammatory diseases. In this field, the dual inhibition of 5-lipoxygenase-activating protein (FLAP) and soluble epoxide hydrolase (sEH) offers the advantage of reducing the production of diverse pro-inflammatory lipid mediators (LMs) while preserving pro-resolving mediator levels. However, this approach is underexplored in medicinal chemistry, given the limited number of existing dual inhibitors. Here, we present the rational design of the adamantylureido-benzylamide aniline 6, which features in vitro FLAP/sEH inhibitory activity. An accurate investigation about the crucial interactions between our synthesized derivatives and 5LOX, FLAP and sEH binding sites, led us to shed light on structural requirements differentiating among the three targets. Lipidomic profiling following 6 in vivo administration highlighted the reduction of 5-LOX/FLAP- and sEH-derived LMs, resulting in a favourable redistribution of LMs in agreement with the inhibition of its molecular targets.
An adamantylureido-benzylamide aniline as FLAP/sEH dual inhibitor: Rational design, in vitro and in vivo lipidomic profiling
Ciaglia, Tania;Di Micco, Simone;Musella, Simona;Di Sarno, Veronica;Merciai, Fabrizio;Smaldone, Gerardina;Di Matteo, Francesca;Pepe, Giacomo;Sommella, Eduardo Maria;Basilicata, Manuela Giovanna;Aquino, Giovanna;Campiglia, Pietro;Ostacolo, Carmine;Bertamino, Alessia
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2025
Abstract
Multitarget approaches are highly effective strategies for treating acute and chronic inflammatory diseases. In this field, the dual inhibition of 5-lipoxygenase-activating protein (FLAP) and soluble epoxide hydrolase (sEH) offers the advantage of reducing the production of diverse pro-inflammatory lipid mediators (LMs) while preserving pro-resolving mediator levels. However, this approach is underexplored in medicinal chemistry, given the limited number of existing dual inhibitors. Here, we present the rational design of the adamantylureido-benzylamide aniline 6, which features in vitro FLAP/sEH inhibitory activity. An accurate investigation about the crucial interactions between our synthesized derivatives and 5LOX, FLAP and sEH binding sites, led us to shed light on structural requirements differentiating among the three targets. Lipidomic profiling following 6 in vivo administration highlighted the reduction of 5-LOX/FLAP- and sEH-derived LMs, resulting in a favourable redistribution of LMs in agreement with the inhibition of its molecular targets.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
