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Bioorganic & Medicinal Chemistry|June 17, 2009
Structure-activity studies on the nociceptin/orphanin FQ receptor antagonist 1-benzyl-N-{3-[spiroisobenzofuran-1(3H),4'-piperidin-1-yl]propyl} pyrrolidine-2-carboxamideClaudio Trapella, Carmela Fischetti, Michela Pela', et al.British Journal of Pharmacology|May 16, 2002
[Nphe1,Arg14,Lys15]nociceptin-NH2, a novel potent and selective antagonist of the nociceptin/orphanin FQ receptorGirolamo Calo, Anna Rizzi, Daniela Rizzi, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 6, 2008
Development of a novel noncompetitive antagonist of IL-1 receptorChristiane Quiniou, Przemyslaw Sapieha, Isabelle Lahaie, et al.Peptides|December 11, 2007
Anxiolytic- and antidepressant-like activities of H-Dmt-Tic-NH-CH(CH2-COOH)-Bid (UFP-512), a novel selective delta opioid receptor agonistRaffaella Vergura, Gianfranco Balboni, Barbara Spagnolo, et al.The Journal of Biological Chemistry|July 9, 2003
Modulation of pro-inflammatory gene expression by nuclear lysophosphatidic acid receptor type-1Fernand Gobeil, Sylvie G Bernier, Alejandro Vazquez-Tello, et al.Nature Medicine|November 29, 2005
Trans-arachidonic acids generated during nitrative stress induce a thrombospondin-1-dependent microvascular degenerationElsa Kermorvant-Duchemin, Florian Sennlaub, Mirna Sirinyan, et al.Bioorganic & Medicinal Chemistry|October 6, 2005
Identification of an achiral analogue of J-113397 as potent nociceptin/orphanin FQ receptor antagonistClaudio Trapella, Remo Guerrini, Laura Piccagli, et al.Journal of Medicinal Chemistry|March 4, 2005
N- and C-terminal modifications of nociceptin/orphanin FQ generate highly potent NOP receptor ligandsRemo Guerrini, Girolamo Caló, David G Lambert, et al.Circulation Research|April 6, 2002
Regulation of eNOS expression in brain endothelial cells by perinuclear EP(3) receptorsFernand Gobeil, Isabelle Dumont, Anne Marilise Marrache, et al.The Journal of Biological Chemistry|May 25, 2006
Structure-activity studies on neuropeptide S: identification of the amino acid residues crucial for receptor activationAdelheid L Roth, Erika Marzola, Anna Rizzi, et al.Pageof 15