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Results: 1-17 |
Results: 17
Coupling of 2,6-disubstituted purines to ribose-modified sugars
Authors: Vittori, S Costanzi, S Lambertucci, C Volpini, R Cristalli, G
Citation: S. Vittori et al., Coupling of 2,6-disubstituted purines to ribose-modified sugars, NUCLEOS NUC, 20(4-7), 2001, pp. 771-774
Synthetic procedure for the preparation of novel potent and selective A(3)adenosine receptor radioligands
Authors: Volpini, R Costanzi, S Lambertucci, C Vittori, S Cristalli, G
Citation: R. Volpini et al., Synthetic procedure for the preparation of novel potent and selective A(3)adenosine receptor radioligands, NUCLEOS NUC, 20(4-7), 2001, pp. 775-779
3 '-Deoxyribofuranose derivatives of 1-deaza and 3-deaza-adenosine and their activity as adenosine deaminase inhibitors
Authors: Costanzi, S Lambertucci, C Volpini, R Vittori, S Lupidi, G Cristalli, G
Citation: S. Costanzi et al., 3 '-Deoxyribofuranose derivatives of 1-deaza and 3-deaza-adenosine and their activity as adenosine deaminase inhibitors, NUCLEOS NUC, 20(4-7), 2001, pp. 1037-1041
Synthesis and adenosine receptor affinity and potency of 8-alkynyl derivatives of adenosine
Authors: Lambertucci, C Costanzi, S Vittori, S Volpini, R Cristalli, G
Citation: C. Lambertucci et al., Synthesis and adenosine receptor affinity and potency of 8-alkynyl derivatives of adenosine, NUCLEOS NUC, 20(4-7), 2001, pp. 1153-1157
Introduction of alkynyl chains on C-8 of adenosine led to very selective antagonists of the A(3) adenosine receptor
Authors: Volpini, R Costanzi, S Lambertucci, C Vittori, S Klotz, KN Lorenzen, A Cristalli, G
Citation: R. Volpini et al., Introduction of alkynyl chains on C-8 of adenosine led to very selective antagonists of the A(3) adenosine receptor, BIOORG MED, 11(14), 2001, pp. 1931-1934
Adenosine deaminase: Functional implications and different classes of inhibitors
Authors: Cristalli, G Costanzi, S Lambertucci, C Lupidi, G Vittori, S Volpini, R Camaioni, E
Citation: G. Cristalli et al., Adenosine deaminase: Functional implications and different classes of inhibitors, MED RES REV, 21(2), 2001, pp. 105-128
N-cycloalkyl derivatives of adenosine and 1-deazaadenosine as agonists andpartial agonists of the A(1) adenosine receptor
Authors: Vittori, S Lorenzen, A Stannek, C Costanzi, S Volpini, R Ijzerman, AP Kunzel, JKVD Cristalli, G
Citation: S. Vittori et al., N-cycloalkyl derivatives of adenosine and 1-deazaadenosine as agonists andpartial agonists of the A(1) adenosine receptor, J MED CHEM, 43(2), 2000, pp. 250-260
Deoxy sugar analogues of triciribine: Correlation of antiviral and antiproliferative activity with intracellular phosphorylation
Authors: Porcari, AR Ptak, RG Borysko, KZ Breitenbach, JM Vittori, S Wotring, LL Drach, JC Townsend, LB
Citation: Ar. Porcari et al., Deoxy sugar analogues of triciribine: Correlation of antiviral and antiproliferative activity with intracellular phosphorylation, J MED CHEM, 43(12), 2000, pp. 2438-2448
Coupling of 2,6-dichloropurine and 2,6-dichlorodeazapurines with ribose and ribose modified sugars
Authors: Vittori, S Camaioni, E Costanzi, S Volpini, R Cristalli, G
Citation: S. Vittori et al., Coupling of 2,6-dichloropurine and 2,6-dichlorodeazapurines with ribose and ribose modified sugars, NUCLEOS NUC, 18(4-5), 1999, pp. 587-590
Synthesis and receptor affinity of polysubstituted adenosines
Authors: Vittori, S Camaioni, E Costanzi, S Volpini, R Klotz, KN Cristalli, G
Citation: S. Vittori et al., Synthesis and receptor affinity of polysubstituted adenosines, NUCLEOS NUC, 18(4-5), 1999, pp. 739-740
Structure-activity relationships of adenosine deaminase inhibitors
Authors: Vittori, S Camaioni, E Costanzi, S Volpini, R Lupidi, G Cristalli, G
Citation: S. Vittori et al., Structure-activity relationships of adenosine deaminase inhibitors, NUCLEOS NUC, 18(4-5), 1999, pp. 741-742
Biological activity of 1-deazapurine nucleosides : Role of deoxycytidine kinase?
Authors: Bergman, AM Cristalli, G Vittori, S Wang, J Eriksson, S Peters, GJ
Citation: Am. Bergman et al., Biological activity of 1-deazapurine nucleosides : Role of deoxycytidine kinase?, NUCLEOS NUC, 18(4-5), 1999, pp. 897-898
Synthesis of di- and tri-substituted adenosine derivatives and their affinities at human adenosine receptor subtypes.
Authors: Volpini, R Camaioni, E Costanzi, S Vittori, S Klotz, KN Cristalli, G
Citation: R. Volpini et al., Synthesis of di- and tri-substituted adenosine derivatives and their affinities at human adenosine receptor subtypes., NUCLEOS NUC, 18(11-12), 1999, pp. 2511-2520
2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A(3) adenosine receptors
Authors: Klotz, KN Camaioni, E Volpini, R Kachler, S Vittori, S Cristalli, G
Citation: Kn. Klotz et al., 2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A(3) adenosine receptors, N-S ARCH PH, 360(2), 1999, pp. 103-108
Synthesis and adenosine deaminase inhibitory activity of 3 '-deoxy-1-deazaadenosines
Authors: Volpini, R Costanzi, S Vittori, S Cristalli, G Lupidi, G
Citation: R. Volpini et al., Synthesis and adenosine deaminase inhibitory activity of 3 '-deoxy-1-deazaadenosines, HELV CHIM A, 82(12), 1999, pp. 2112-2118
Characterization of potent ligands at human recombinant adenosine receptors
Authors: Cristalli, G Camaioni, E Costanzi, S Vittori, S Volpini, R Klotz, KN
Citation: G. Cristalli et al., Characterization of potent ligands at human recombinant adenosine receptors, DRUG DEV R, 45(3-4), 1998, pp. 176-181
Synthesis of new 3 '-deoxyribonucleosides employing the acid-catalyzed fusion method
Authors: Volpini, R Camaioni, E Costanzi, S Vittori, S Cristalli, G
Citation: R. Volpini et al., Synthesis of new 3 '-deoxyribonucleosides employing the acid-catalyzed fusion method, HELV CHIM A, 81(12), 1998, pp. 2326-2331
Risultati: 1-17 |