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Results: 1-25 | 26-37
Results: 1-25/37
Novel inhibitors of cholesterol biosynthesis
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, Novel inhibitors of cholesterol biosynthesis, DRUG DISC T, 6(8), 2001, pp. 438-438
A selenopyrylium photosensitizer for photodynamic therapy
Authors: Walker, MA Barlocco, D
Citation: Ma. Walker et D. Barlocco, A selenopyrylium photosensitizer for photodynamic therapy, DRUG DISC T, 6(7), 2001, pp. 377-378
Quinolizin-2-one derivatives as novel hypoglycaemic agents
Authors: Langston, S Barlocco, D
Citation: S. Langston et D. Barlocco, Quinolizin-2-one derivatives as novel hypoglycaemic agents, DRUG DISC T, 6(6), 2001, pp. 326-326
A potent photoaffinity probe inhibitor of PDE4
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, A potent photoaffinity probe inhibitor of PDE4, DRUG DISC T, 6(5), 2001, pp. 268-269
Potent M-2 muscarinic receptor antagonists
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, Potent M-2 muscarinic receptor antagonists, DRUG DISC T, 6(5), 2001, pp. 268-268
Novel dual antagonists of neurokinin receptors 1 and 2
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, Novel dual antagonists of neurokinin receptors 1 and 2, DRUG DISC T, 6(5), 2001, pp. 269-269
Inhibitors of lipoprotein-associated phospholipase A(2)
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, Inhibitors of lipoprotein-associated phospholipase A(2), DRUG DISC T, 6(5), 2001, pp. 269-270
Heterocyclic-fused quinoxalinones as selective antagonists at the AMPA receptor
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, Heterocyclic-fused quinoxalinones as selective antagonists at the AMPA receptor, DRUG DISC T, 6(5), 2001, pp. 270-270
The spirooxazolidinone moiety as a potential substrate for selective agonists at the alpha 7 nicotinic acetylcholine receptor
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, The spirooxazolidinone moiety as a potential substrate for selective agonists at the alpha 7 nicotinic acetylcholine receptor, DRUG DISC T, 6(5), 2001, pp. 270-271
Non-peptidic blockers of apamin-sensitive Ca2+-activated K+-channels
Authors: Barrett, D Barlocco, D
Citation: D. Barrett et D. Barlocco, Non-peptidic blockers of apamin-sensitive Ca2+-activated K+-channels, DRUG DISC T, 6(3), 2001, pp. 159-159
Guanine analogues as phosphodiesterase 7 (PDE7) inhibitors
Authors: Barlocco, D
Citation: D. Barlocco, Guanine analogues as phosphodiesterase 7 (PDE7) inhibitors, DRUG DISC T, 6(16), 2001, pp. 859-859
P38 MAP kinase inhibitors for the treatment of arthritis
Authors: Barlocco, D Langston, S
Citation: D. Barlocco et S. Langston, P38 MAP kinase inhibitors for the treatment of arthritis, DRUG DISC T, 6(15), 2001, pp. 808-809
D-Morphine: possible clinical implications for the management of neuropathic pain
Authors: Langston, S Barlocco, D
Citation: S. Langston et D. Barlocco, D-Morphine: possible clinical implications for the management of neuropathic pain, DRUG DISC T, 6(14), 2001, pp. 746-747
Novel ibutilide analogues for the treatment of re-entrant cardiac arrhythmias
Authors: Langston, S Barlocco, D
Citation: S. Langston et D. Barlocco, Novel ibutilide analogues for the treatment of re-entrant cardiac arrhythmias, DRUG DISC T, 6(13), 2001, pp. 698-699
Tricyclic oximino derivatives as novel 5-HT3 ligands
Authors: Barlocco, D
Citation: D. Barlocco, Tricyclic oximino derivatives as novel 5-HT3 ligands, DRUG DISC T, 6(12), 2001, pp. 647-647
Imidazolylmethylthiophenes as potential analgesic agents
Authors: Barlocco, D
Citation: D. Barlocco, Imidazolylmethylthiophenes as potential analgesic agents, DRUG DISC T, 6(12), 2001, pp. 647-648
Pyrazolo[1,5-a]pyrimidines as novel COX-2 selective inhibitors
Authors: Barlocco, D
Citation: D. Barlocco, Pyrazolo[1,5-a]pyrimidines as novel COX-2 selective inhibitors, DRUG DISC T, 6(11), 2001, pp. 595-595
Azidopyridinyl compounds as candidate photoaffinity probes for nicotinic acetylcholine receptors
Authors: Langston, S Barlocco, D
Citation: S. Langston et D. Barlocco, Azidopyridinyl compounds as candidate photoaffinity probes for nicotinic acetylcholine receptors, DRUG DISC T, 6(10), 2001, pp. 547-547
3,8-Diazabicyclo-[3.2.1]-octane derivatives as analogues of ambasilide, a Class III antiarrhythmic agent
Authors: Villa, S Barlocco, D Cignarella, G Papp, GJ Balati, B Takacs, J Varro, A Borosy, A Keseru, K Matyus, M
Citation: S. Villa et al., 3,8-Diazabicyclo-[3.2.1]-octane derivatives as analogues of ambasilide, a Class III antiarrhythmic agent, EUR J MED C, 36(6), 2001, pp. 495-506
5,6-diphenylpyridazine derivatives as acyl-CoA : cholesterol acyltransferase inhibitors
Authors: Giovannoni, MP Dal Piaz, V Kwon, BM Kim, MK Kim, YK Toma, L Barlocco, D Bernini, F Canavesi, M
Citation: Mp. Giovannoni et al., 5,6-diphenylpyridazine derivatives as acyl-CoA : cholesterol acyltransferase inhibitors, J MED CHEM, 44(24), 2001, pp. 4292-4295
Phenylpiperazinylalkylamino substituted pyridazinones as potent alpha(1) adrenoceptor antagonists
Authors: Barlocco, D Cignarella, G Dal Piaz, V Giovannoni, MP De Benedetti, PG Fanelli, F Montesano, F Poggesi, E Leonardi, A
Citation: D. Barlocco et al., Phenylpiperazinylalkylamino substituted pyridazinones as potent alpha(1) adrenoceptor antagonists, J MED CHEM, 44(15), 2001, pp. 2403-2410
Pharmacological approaches to the treatment of diabetic complications
Authors: Costantino, L Rastelli, G Gamberini, MC Barlocco, D
Citation: L. Costantino et al., Pharmacological approaches to the treatment of diabetic complications, EXPERT OP T, 10(8), 2000, pp. 1245-1262
5,6-dinitrophenyl and 5-aminophenyl-6-nitrophenyl analogues of the ACAT inhibitor 5,6-diphenyl-3-alkylaminopyridazines
Authors: Toma, L Nava, D Celentano, G Giovannoni, MP Dal Piaz, V Kwon, BM Kim, MK Kim, YK Barlocco, D
Citation: L. Toma et al., 5,6-dinitrophenyl and 5-aminophenyl-6-nitrophenyl analogues of the ACAT inhibitor 5,6-diphenyl-3-alkylaminopyridazines, HETEROCYCLE, 53(12), 2000, pp. 2709
Structural and conformational studies of 3,8-diazabicyclo[3.2.1]octane derivatives, selective agonists of mu-opioid receptors
Authors: Artali, R Barlocco, D Bombieri, G Cignarella, G Meneghetti, F
Citation: R. Artali et al., Structural and conformational studies of 3,8-diazabicyclo[3.2.1]octane derivatives, selective agonists of mu-opioid receptors, HETEROCYCLE, 53(11), 2000, pp. 2403
The opioid-receptor-like 1 (ORL-1) as a potential target for new analgesics
Authors: Barlocco, D Cignarella, G Giardina, GAM Toma, L
Citation: D. Barlocco et al., The opioid-receptor-like 1 (ORL-1) as a potential target for new analgesics, EUR J MED C, 35(3), 2000, pp. 275-282
Risultati: 1-25 | 26-37