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Il Farmaco; Edizione Scientifica|March 1, 1987
[C-alkylpiperazines. XII. Synthesis and diuretic activity of compounds structurally related to clopamide]L Landriani, D Barlocco, G Cignarella, et al.Il Farmaco; Edizione Scientifica|March 1, 1983
6-Halogen derivatives of 2-(3-benzoylphenyl)propionic acidG Cignarella, M M Curzu, G Grella, et al.Il Farmaco; Edizione Scientifica|February 1, 1982
[Unexpected anti-inflammatory activity of rigid structures derived from antihypertensive 6-arylpyridazinones. III. Synthesis and activity of 7-fluoro- and 5-keto-5H-indeno(1,2-c)pyridozines]G Cignarella, M Loriga, G A Pinna, et al.Drug Design and Discovery|April 1, 1997
Thienocycloheptapyridazines as new muscarinic agentsD Barlocco, G Cignarella, F Fanelli, et al.Journal of Medicinal Chemistry|November 1, 1986
Conformationally restricted congeners of hypotensive and platelet aggregation inhibitors: 6-aryl-5-methyl-4,5-dihydro-3(2H)-pyridazinones derived from 5H-indeno[1,2-c]pyridazineG Cignarella, D Barlocco, G A Pinna, et al.Farmaco (Societa Chimica Italiana : 1989)|March 19, 1999
Synthesis and mu-opioid receptor affinity of a new series of nitro substituted 3,8-diazabicyclo[3.2.1]octane derivativesD Barlocco, G Cignarella, P Vianello, et al.Il Farmaco; Edizione Scientifica|February 1, 1988
New congeners of antihypertensive and antithrombotic 7-amino or 7-acetyl-aminosubstituted-4,4a-dihydro-5H-indeno (1,2-c)pyridazin-3-onesG Cignarella, D Barlocco, L Landriani, et al.Farmaco (Societa Chimica Italiana : 1989)|April 1, 1992
Synthesis and pharmacological activity of 4-carbamoyl-5-aryl-6-methyl-4,5-dihydropyridazin-3(2H)-onesG A Pinna, F Sardu, M M Curzu, et al.Neuroscience|February 15, 2005
Gamma-hydroxybutyric acid (GHB) and the mesoaccumbens reward circuit: evidence for GABA(B) receptor-mediated effectsM Pistis, A L Muntoni, G Pillolla, et al.Il Farmaco; Edizione Scientifica|June 1, 1988
Synthesis and pharmacological study of 5-aryl-6-methyl-4,5-dihydro-pyridazin-3(2H)ones and related 5-aryl-6-methyl-pyridazin-3(2H)onesG A Pinna, M M Curzu, D Barlocco, et al.Pageof 5