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Results: 1-8 |
Results: 8
FREE-ENERGY PERTURBATION STUDIES ON BINDING OF THE INHIBITOR 5,6-DIHYDROBENZO[H]CINNOLIN-3(2H)ONE-2-ACETIC ACID AND ITS METHOXYLATED ANALOGS TO ALDOSE REDUCTASE
Authors: RASTELLI G COSTANTINO L VIANELLO P BARLOCCO D
Citation: G. Rastelli et al., FREE-ENERGY PERTURBATION STUDIES ON BINDING OF THE INHIBITOR 5,6-DIHYDROBENZO[H]CINNOLIN-3(2H)ONE-2-ACETIC ACID AND ITS METHOXYLATED ANALOGS TO ALDOSE REDUCTASE, Tetrahedron, 54(32), 1998, pp. 9415-9428
MONOSUBSTITUTED-3,8-DIAZABICYCLO[3.2.1]OCTANE AND DISUBSTITUTED-3,8-DIAZABICYCLO[3.2.1]OCTANE DERIVATIVES AS ANALGESICS STRUCTURALLY RELATED TO EPIBATIDINE - SYNTHESIS, ACTIVITY, AND MODELING
Authors: BARLOCCO D CIGNARELLA G TONDI D VIANELLO P VILLA S BARTOLINI A GHELARDINI C GALEOTTI N ANDERSON DJ KUNTZWEILER TA COLOMBO D TOMA L
Citation: D. Barlocco et al., MONOSUBSTITUTED-3,8-DIAZABICYCLO[3.2.1]OCTANE AND DISUBSTITUTED-3,8-DIAZABICYCLO[3.2.1]OCTANE DERIVATIVES AS ANALGESICS STRUCTURALLY RELATED TO EPIBATIDINE - SYNTHESIS, ACTIVITY, AND MODELING, Journal of medicinal chemistry, 41(5), 1998, pp. 674-681
GENERATION OF SPECIFIC DEOXYNOJIRIMYCIN-TYPE INHIBITORS OF THE NONLYSOSOMAL GLUCOSYLCERAMIDASE
Authors: OVERKLEEFT HS RENKEMA GH NEELE J VIANELLO P HUNG IO STRIJLAND A VANDERBURG AM KOOMEN GJ PANDIT UK AERTS JMFG
Citation: Hs. Overkleeft et al., GENERATION OF SPECIFIC DEOXYNOJIRIMYCIN-TYPE INHIBITORS OF THE NONLYSOSOMAL GLUCOSYLCERAMIDASE, The Journal of biological chemistry, 273(41), 1998, pp. 26522-26527
NEW ALDOSE REDUCTASE INHIBITORS AS POTENTIAL AGENTS FOR THE PREVENTION OF LONG-TERM DIABETIC COMPLICATIONS
Authors: COSTANTINO L RASTELLI G CIGNARELLA G VIANELLO P BARLOCCO D
Citation: L. Costantino et al., NEW ALDOSE REDUCTASE INHIBITORS AS POTENTIAL AGENTS FOR THE PREVENTION OF LONG-TERM DIABETIC COMPLICATIONS, Expert opinion on therapeutic patents, 7(8), 1997, pp. 843-858
STUDY OF THE ANTISECRETORY AND ANTIULCER MECHANISMS OF A NEW INDENOPIRYDAZINONE DERIVATIVE IN RATS
Authors: BAROCELLI E CHIAVARINI M BALLABENI V BARLOCCO D VIANELLO P DALPIAZ V IMPICCIATORE M
Citation: E. Barocelli et al., STUDY OF THE ANTISECRETORY AND ANTIULCER MECHANISMS OF A NEW INDENOPIRYDAZINONE DERIVATIVE IN RATS, Pharmacological research, 35(5), 1997, pp. 487-492
STRUCTURE-BASED DESIGN OF AN INHIBITOR MODELED AT THE SUBSTRATE ACTIVE-SITE OF ALDOSE REDUCTASE
Authors: RASTELLI G VIANELLO P BARLOCCO D COSTANTINO L DELCORSO A MURA U
Citation: G. Rastelli et al., STRUCTURE-BASED DESIGN OF AN INHIBITOR MODELED AT THE SUBSTRATE ACTIVE-SITE OF ALDOSE REDUCTASE, Bioorganic & medicinal chemistry letters, 7(14), 1997, pp. 1897-1902
SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF DERIVATIVES STRUCTURALLY RELATED TO NIMESULIDE
Authors: CIGNARELLA G VIANELLO P BERTI F ROSSONI G
Citation: G. Cignarella et al., SYNTHESIS AND PHARMACOLOGICAL EVALUATION OF DERIVATIVES STRUCTURALLY RELATED TO NIMESULIDE, European journal of medicinal chemistry, 31(5), 1996, pp. 359-364
SYNTHESIS, ACTIVITY, AND MOLECULAR MODELING OF A NEW SERIES OF TRICYCLIC PYRIDAZINONES AS SELECTIVE ALDOSE REDUCTASE INHIBITORS
Authors: COSTANTINO L RASTELLI G VESCOVINI K CIGNARELLA G VIANELLO P DELCORSO A CAPPIELLO M MURA U BARLOCCO D
Citation: L. Costantino et al., SYNTHESIS, ACTIVITY, AND MOLECULAR MODELING OF A NEW SERIES OF TRICYCLIC PYRIDAZINONES AS SELECTIVE ALDOSE REDUCTASE INHIBITORS, Journal of medicinal chemistry, 39(22), 1996, pp. 4396-4405
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