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Molecular Pharmacology|July 22, 2004
"Induced-fit" mechanism for catecholamine binding to the beta2-adrenergic receptorRenata Del Carmine, Paola Molinari, Maria Sbraccia, et al.
The Journal of Biological Chemistry|February 25, 2003
Promiscuous coupling at receptor-Galpha fusion proteins. The receptor of one covalent complex interacts with the alpha-subunit of anotherPaola Molinari, Caterina Ambrosio, Daniela Riitano, et al.
Archiv Der Pharmazie|January 9, 2007
Synthesis of new 4-heteroaryl-2-phenylquinolines and their pharmacological activity as NK-2/NK-3 receptor ligandsAnna Borioni, Carlo Mustazza, Isabella Sestili, et al.
European Journal of Medicinal Chemistry|February 19, 2011
Synthesis and pharmacological evaluation of bivalent antagonists of the nociceptin opioid receptorMaria Rosaria Del Giudice, Anna Borioni, Giuditta Bastanzio, et al.
The Journal of Biological Chemistry|April 23, 2005
Different structural requirements for the constitutive and the agonist-induced activities of the beta2-adrenergic receptorCaterina Ambrosio, Paola Molinari, Francesca Fanelli, et al.
British Journal of Pharmacology|April 6, 2002
Mutations inducing divergent shifts of constitutive activity reveal different modes of binding among catecholamine analogues to the beta(2)-adrenergic receptorRenata Del Carmine, Caterina Ambrosio, Maria Sbraccia, et al.
Journal of Medicinal Chemistry|February 1, 2008
Synthesis and pharmacological evaluation of 1,2-dihydrospiro[isoquinoline-4(3H),4'-piperidin]-3-ones as nociceptin receptor agonistsCarlo Mustazza, Anna Borioni, Isabella Sestili, et al.
The Journal of Biological Chemistry|March 2, 2010
Morphine-like opiates selectively antagonize receptor-arrestin interactionsPaola Molinari, Vanessa Vezzi, Maria Sbraccia, et al.
Chemical & Pharmaceutical Bulletin|May 3, 2006
Synthesis and evaluation as NOP ligands of some spiro[piperidine-4,2'(1'H)-quinazolin]-4'(3'H)-ones and spiro[piperidine-4,5'(6'H)-[1,2,4]triazolo[1,5-c]quinazolines]Carlo Mustazza, Anna Borioni, Isabella Sestili, et al.
European Journal of Medicinal Chemistry|December 2, 2004
A new synthetic approach of N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamide (JTC-801) and its analogues and their pharmacological evaluation as nociceptin receptor (NOP) antagonistsIsabella Sestili, Anna Borioni, Carlo Mustazza, et al.
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