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European Journal of Medicinal Chemistry|March 2, 2019
(2S)-N-2-methoxy-2-phenylethyl-6,7-benzomorphan compound (2S-LP2): Discovery of a biased mu/delta opioid receptor agonistLorella Pasquinucci, Rita Turnaturi, Girolamo Calò, et al.
Toxicology and Applied Pharmacology|May 7, 2026
An innovative label-free approach for investigating epithelial-mesenchymal transition: pharmacological characterization of TGF-β1 effects in A549 cellsFrancine Medjiofack Djeujo, Marco Solimano Negrini, Pietro Ferri, et al.
European Journal of Pharmacology|May 10, 2006
In vitro and in vivo pharmacological characterization of the nociceptin/orphanin FQ receptor ligand Ac-RYYRIK-olOzge Gündüz, Anna Rizzi, Anna Baldisserotto, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|March 19, 2013
Nociceptin/orphanin FQ receptor activation decreases the airway hyperresponsiveness induced by allergen in sensitized miceNikol Sullo, Fiorentina Roviezzo, Maria Matteis, et al.
Bioorganic Chemistry|August 3, 2021
Selective MOR activity of DAPEA and Endomorphin-2 analogues containing a (R)-γ-Freidinger lactam in position twoAlice Della Valle, Azzurra Stefanucci, Giuseppe Scioli, et al.
The Journal of Pharmacology and Experimental Therapeutics|October 31, 2008
In vitro and in vivo pharmacological characterization of the neuropeptide s receptor antagonist [D-Cys(tBu)5]neuropeptide SValeria Camarda, Anna Rizzi, Chiara Ruzza, et al.
Journal of Medicinal Chemistry|December 31, 2008
Synthesis and biological activity of human neuropeptide S analogues modified in position 5: identification of potent and pure neuropeptide S receptor antagonistsRemo Guerrini, Valeria Camarda, Claudio Trapella, et al.
European Journal of Pharmacology|August 11, 2024
In vitro pharmacological characterization of growth hormone secretagogue receptor ligands using the dynamic mass redistribution and calcium mobilization assaysChiara Sturaro, Chiara Ruzza, Federica Ferrari, et al.
Bioconjugate Chemistry|August 29, 2019
Tetrabranched Hetero-Conjugated Peptides as Bifunctional Agonists of the NOP and Mu Opioid ReceptorsSalvatore Pacifico, Valentina Albanese, Davide Illuminati, et al.
Bioorganic & Medicinal Chemistry|May 11, 2007
Synthesis and biological activity of nociceptin/orphanin FQ analogues substituted in position 7 or 11 with Calpha,alpha-dialkylated amino acidsMarika Arduin, Barbara Spagnolo, Girolamo Calò, et al.
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