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Results: 1-7 |
Results: 7
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
Synthesis and NMR-driven conformational analysis of taxol analogues conformationally constrained on the C13 side chain
Authors: Barboni, L Lambertucci, C Appendino, G Vander Velde, DG Himes, RH Bombardelli, E Wang, MM Snyder, JP
Citation: L. Barboni et al., Synthesis and NMR-driven conformational analysis of taxol analogues conformationally constrained on the C13 side chain, J MED CHEM, 44(10), 2001, pp. 1576-1587
Risultati: 1-7 |