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Results: 1-25 | 26-37 |
Results: 26-37/37
Structures and reactivities of 1-oxo-cycloalkan-2-ylideneacetic acids. A H-1 NMR, modelling and photochemical study
Authors: Ghelli, S Costi, MP Toma, L Barlocco, D Ponterini, G
Citation: S. Ghelli et al., Structures and reactivities of 1-oxo-cycloalkan-2-ylideneacetic acids. A H-1 NMR, modelling and photochemical study, TETRAHEDRON, 56(38), 2000, pp. 7561-7571
A series of diarylsubstituted oximes as potential substrate for new aldosereductase inhibitors
Authors: Rakowitz, D Heinisch, G Lukavsky, P Kiendler, S Trenkwalder, C Barlocco, D Rastelli, G Costantino, L
Citation: D. Rakowitz et al., A series of diarylsubstituted oximes as potential substrate for new aldosereductase inhibitors, J HETERO CH, 37(5), 2000, pp. 1089-1096
Synthesis and aldose reductase inhibitory activity of a new series of benzo[h]cinnolinone derivatives
Authors: Costantino, L Rastelli, G Cignarella, G Barlocco, D
Citation: L. Costantino et al., Synthesis and aldose reductase inhibitory activity of a new series of benzo[h]cinnolinone derivatives, FARMACO, 55(8), 2000, pp. 544-552
Diabetes complications and their potential prevention: Aldose reductase inhibition and other approaches
Authors: Costantino, L Rastelli, G Vianello, P Cignarella, G Barlocco, D
Citation: L. Costantino et al., Diabetes complications and their potential prevention: Aldose reductase inhibition and other approaches, MED RES REV, 19(1), 1999, pp. 3-23
Phthalein derivatives as a new tool for selectivity in thymidylate synthase
Authors: Costi, PM Rinaldi, M Tondi, D Pecorari, P Barlocco, D Ghelli, S Stroud, RM Santi, DV Stout, TJ Musiu, C Marangiu, EM Pani, A Congiu, D Loi, GA La Colla, P
Citation: Pm. Costi et al., Phthalein derivatives as a new tool for selectivity in thymidylate synthase, J MED CHEM, 42(12), 1999, pp. 2112-2124
Isoxazolo-[3,4-d]-pyridazin-7-(6H)-one as a potential substrate for new aldose reductase inhibitors
Authors: Costantino, L Rastelli, G Gamberini, MC Giovannoni, MP Dal Piaz, V Vianello, P Barlocco, D
Citation: L. Costantino et al., Isoxazolo-[3,4-d]-pyridazin-7-(6H)-one as a potential substrate for new aldose reductase inhibitors, J MED CHEM, 42(11), 1999, pp. 1894-1900
Novel adrenoceptor antagonists with a tricyclic pyrrolodipyridazine skeleton
Authors: Barlocco, D Cignarella, G Montesano, F Leonardi, A Mella, M Toma, L
Citation: D. Barlocco et al., Novel adrenoceptor antagonists with a tricyclic pyrrolodipyridazine skeleton, J MED CHEM, 42(1), 1999, pp. 173-177
Separation, structural determination and biological evaluation of the thymidylate synthase inhibitor 3,3-di-(4 '-hydroxyphenyl)-6(7)-chloro-1-oxo-1H,3H-naphtho[1,8-cd]pyran
Authors: Costi, MP Tondi, D Pecorari, P Rinaldi, M Celentano, G Ghelli, S Antolini, L Barlocco, D
Citation: Mp. Costi et al., Separation, structural determination and biological evaluation of the thymidylate synthase inhibitor 3,3-di-(4 '-hydroxyphenyl)-6(7)-chloro-1-oxo-1H,3H-naphtho[1,8-cd]pyran, J HETERO CH, 36(4), 1999, pp. 1043-1048
Structure-based design of inhibitors specific for bacterial thymidylate synthase
Authors: Stout, TJ Tondi, D Rinaldi, M Barlocco, D Pecorari, P Santi, DV Kuntz, ID Stroud, RM Shoichet, BK Costi, MP
Citation: Tj. Stout et al., Structure-based design of inhibitors specific for bacterial thymidylate synthase, BIOCHEM, 38(5), 1999, pp. 1607-1617
Antiamnesic activity of the nicotinic agonist DBO-83 in mice
Authors: Ghelardini, C Galeotti, N Giuliani, F Barlocco, D Bartolini, A
Citation: C. Ghelardini et al., Antiamnesic activity of the nicotinic agonist DBO-83 in mice, DRUG DEV R, 45(2), 1998, pp. 45-51
Synthesis and mu-opioid receptor affinity of a new series of nitro substituted 3,8-diazabicyclo[3.2.1]octane derivatives
Authors: Barlocco, D Cignarella, G Vianello, P Villa, S Pinna, GA Fadda, P Fratta, W
Citation: D. Barlocco et al., Synthesis and mu-opioid receptor affinity of a new series of nitro substituted 3,8-diazabicyclo[3.2.1]octane derivatives, FARMACO, 53(8-9), 1998, pp. 557-562
Benzocondensed derivatives as rigid analogues of the mu-opioid agonist 3(8)-cinnamyl-8(3)-propionyl-3,8-diazabicyclo[3.2.1]octanes: synthesis, modeling, and affinity
Authors: Cignarella, G Barlocco, D Vianello, P Villa, S Pinna, GA Fadda, P Fratta, W Toma, L Gessi, S
Citation: G. Cignarella et al., Benzocondensed derivatives as rigid analogues of the mu-opioid agonist 3(8)-cinnamyl-8(3)-propionyl-3,8-diazabicyclo[3.2.1]octanes: synthesis, modeling, and affinity, FARMACO, 53(10-11), 1998, pp. 667-674
Risultati: 1-25 | 26-37 |