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Chemical & Pharmaceutical Bulletin|June 5, 2002
Synthesis and cytotoxic activities of pyrrole[2,3-d]pyridazin-4-one derivativesGabriele Murineddu, Giorgio Cignarella, Giorgio Chelucci, et al.Farmaco (Societa Chimica Italiana : 1989)|September 19, 2003
Congo red analogues as potential anti-prion agentsStefania Villa, Giorgio Cignarella, Daniela Barlocco, et al.European Journal of Pharmacology|July 6, 2002
Stereoselectivity of NCS-382 binding to gamma-hydroxybutyrate receptor in the rat brainM Paola Castelli, Ignazia Mocci, Marco Pistis, et al.Bioorganic & Medicinal Chemistry|April 9, 2002
N-3(9)-arylpropenyl-N-9(3)-propionyl-3,9-diazabicyclo[3.3.1]nonanes as mu-opioid receptor agonists. Effects on mu-affinity of arylalkenyl chain modificationsGérard A Pinna, Giorgio Cignarella, Giovanni Loriga, et al.Journal of Medicinal Chemistry|August 23, 2002
6-Chloropyridazin-3-yl derivatives active as nicotinic agents: synthesis, binding, and modeling studiesLucio Toma, Paolo Quadrelli, William H Bunnelle, et al.Bioorganic & Medicinal Chemistry|October 26, 2005
Synthesis of 3,6-diazabicyclo[3.1.1]heptanes as novel ligands for the opioid receptorsGiovanni Loriga, Ilaria Manca, Gabriele Murineddu, et al.European Journal of Pharmacology|June 14, 2002
Central effects of 1,4-butanediol are mediated by GABA(B) receptors via its conversion into gamma-hydroxybutyric acidMauro A M Carai, Giancarlo Colombo, Roberta Reali, et al.Bioorganic & Medicinal Chemistry|August 21, 2003
Synthesis of novel diazatricyclodecanes (DTDs). Effects of structural variation at the C3' allyl end and at the phenyl ring of the cinnamyl chain on mu-receptor affinity and opioid antinociceptionGérard Aimè Pinna, Giorgio Cignarella, Stefania Ruiu, et al.Chemmedchem|March 18, 2009
Synthesis, modelling, and antimitotic properties of tricyclic systems characterised by a 2-(5-Phenyl-1H-pyrrol-3-yl)-1,3,4-oxadiazole moietyGérard A Pinna, Gabriele Murineddu, Caterina Murruzzu, et al.Journal of Medicinal Chemistry|April 2, 2004
Synthesis, screening, and molecular modeling of new potent and selective antagonists at the alpha 1d adrenergic receptorAmedeo Leonardi, Daniela Barlocco, Federica Montesano, et al.Pageof 2