-
1
-
-
0013463887
-
Adenosine receptors: Medicinal chemistry, pharmacology and therapeutic applications
-
G. Cristalli, R. Volpini (ed.), Adenosine Receptors: Medicinal Chemistry, Pharmacology and Therapeutic Applications, Current Topics in Medicinal Chemistry, 3 (2003) 355-469.
-
(2003)
Current Topics in Medicinal Chemistry
, vol.3
, pp. 355-469
-
-
Cristalli, G.1
Volpini, R.2
-
2
-
-
0036315203
-
Adenine and deazaadenine nucleoside and deoxy-nucleoside analogues: inhibition of viral replication of sheep MVV (in vitro model for HIV) and bovine BHV-1
-
D. Salvatori, R. Volpini, S. Vincenzetti, A. Vita, S. Costanzi, C. Lambertucci, G. Cristalli, S. Vittori, Adenine and deazaadenine nucleoside and deoxy-nucleoside analogues: inhibition of viral replication of sheep MVV (in vitro model for HIV) and bovine BHV-1, Bioorg. Med. Chem., 10 (2002) 2973-2980.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 2973-2980
-
-
Salvatori, D.1
Volpini, R.2
Vincenzetti, S.3
Vita, A.4
Costanzi, S.5
Lambertucci, C.6
Cristalli, G.7
Vittori, S.8
-
3
-
-
0035120798
-
Adenosine deaminase: Functional implication and different classis of inhibitors
-
Cristalli G., Costanzi S., Lambertucci C., Lupidi G., Vittori S., Volpini R., Camaioni E. Adenosine deaminase: functional implication and different classis of inhibitors. Med. Res. Rev. 21:2001;105-128.
-
(2001)
Med. Res. Rev.
, vol.21
, pp. 105-128
-
-
Cristalli, G.1
Costanzi, S.2
Lambertucci, C.3
Lupidi, G.4
Vittori, S.5
Volpini, R.6
Camaioni, E.7
-
4
-
-
0025733977
-
Purine and 1-deazapurine ribonucleosides and deoxyribonucleosides: Synthesis and biological activity
-
Cristalli G., Vittori S., Eleuteri A., Grifantini M., Volpini R., Lupidi G., Capolongo L., Pesenti E. Purine and 1-deazapurine ribonucleosides and deoxyribonucleosides: synthesis and biological activity. J. Med. Chem. 33:1991;2226-2230.
-
(1991)
J. Med. Chem.
, vol.33
, pp. 2226-2230
-
-
Cristalli, G.1
Vittori, S.2
Eleuteri, A.3
Grifantini, M.4
Volpini, R.5
Lupidi, G.6
Capolongo, L.7
Pesenti, E.8
-
5
-
-
0028874506
-
6-cycloalkyl derivatives of 1-deazapurine nucleosides: A new class of anti-immunodeficiency virus agents
-
6-cycloalkyl derivatives of 1-deazapurine nucleosides: a new class of anti-immunodeficiency virus agents. J. Med. Chem. 38:1995;4019-4025.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4019-4025
-
-
Cristalli, G.1
Vittori, S.2
Eleuteri, A.3
Volpini, R.4
Camaioni, E.5
Lupidi, G.6
Mahmood, N.7
Bevilacqua, F.8
Palu, G.9
-
6
-
-
0030816839
-
Potent and selective ligand for adenosine binding site
-
Cristalli G., Camaioni E., Di Francesco E., Eleuteri A., Vittori S., Volpini R. Potent and selective ligand for adenosine binding site. Nucleosides Nucleotides. 16:1997;1379-1388.
-
(1997)
Nucleosides Nucleotides
, vol.16
, pp. 1379-1388
-
-
Cristalli, G.1
Camaioni, E.2
Di Francesco, E.3
Eleuteri, A.4
Vittori, S.5
Volpini, R.6
-
7
-
-
0032443699
-
Synthesis of new 3′-deoxy ribonucleosides employing the acid-catalyzed fusion method
-
Volpini R., Camaioni E., Costanzi S., Vittori S., Cristalli G. Synthesis of new 3′-deoxy ribonucleosides employing the acid-catalyzed fusion method. Helv. Chim. Acta. 81:1998;2326-2331.
-
(1998)
Helv. Chim. Acta
, vol.81
, pp. 2326-2331
-
-
Volpini, R.1
Camaioni, E.2
Costanzi, S.3
Vittori, S.4
Cristalli, G.5
-
8
-
-
0033403282
-
Synthesis and adenosine deaminase inhibitory activity of 3′-deoxy-1-deazaadenosines
-
Volpini R., Camaioni E., Costanzi S., Vittori S., Lupidi G., Cristalli G. Synthesis and adenosine deaminase inhibitory activity of 3′-deoxy-1-deazaadenosines. Helv. Chim. Acta. 82:1999;2212-2218.
-
(1999)
Helv. Chim. Acta
, vol.82
, pp. 2212-2218
-
-
Volpini, R.1
Camaioni, E.2
Costanzi, S.3
Vittori, S.4
Lupidi, G.5
Cristalli, G.6
-
9
-
-
0034719504
-
-6-substituted-2′-deoxyadenosines
-
-6-substituted-2′-deoxyadenosines. J. Med. Chem. 43:2000;250-260.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 250-260
-
-
Vittori, S.1
Lorenzen, A.2
Stannek, C.3
Costanzi, S.4
Volpini, R.5
IJerman, A.P.6
Von Frijtag Drabble Kunzel, J.K.7
Cristalli, G.8
-
10
-
-
0022350786
-
Adenosine and 2-chloroadenosine deaza-analogues as adenosine receptor agonists
-
Cristalli G., Grifantini M., Vittori S., Balduini W., Cattabeni F. Adenosine and 2-chloroadenosine deaza-analogues as adenosine receptor agonists. Nucleosides Nucleotides. 4:1985;625-639.
-
(1985)
Nucleosides Nucleotides
, vol.4
, pp. 625-639
-
-
Cristalli, G.1
Grifantini, M.2
Vittori, S.3
Balduini, W.4
Cattabeni, F.5
-
11
-
-
0027402156
-
Synthesis of 1,7-dideazapurine ribonucleosides and deoxyribonucleosides
-
Cristalli G., Vittori S., Eleuteri A., Volpini R., Cola D., Camaioni E., Gariboldi P.V., Lupidi G. Synthesis of 1,7-dideazapurine ribonucleosides and deoxyribonucleosides. Nucleosides Nucleotides. 12:1993;39-53.
-
(1993)
Nucleosides Nucleotides
, vol.12
, pp. 39-53
-
-
Cristalli, G.1
Vittori, S.2
Eleuteri, A.3
Volpini, R.4
Cola, D.5
Camaioni, E.6
Gariboldi, P.V.7
Lupidi, G.8
-
12
-
-
85031211781
-
Deaza and deoxy adenosine derivatives: Synthesis and inhibition of animal viruses as human infection models
-
in press
-
S. Vittori, S. Costanzi, C. Lambertucci, S. Taffi, R. Volpini, G. Cristalli, Deaza and deoxy adenosine derivatives: synthesis and inhibition of animal viruses as human infection models, Nucleos Nucleot Nucl (in press).
-
Nucleos Nucleot Nucl
-
-
Vittori, S.1
Costanzi, S.2
Lambertucci, C.3
Taffi, S.4
Volpini, R.5
Cristalli, G.6
-
13
-
-
0003964990
-
-
Hypercube Inc., USA
-
HYPERCHEM 5.02, Hypercube Inc., USA, 1997.
-
(1997)
HYPERCHEM 5.02
-
-
-
14
-
-
0031776418
-
New substituted 9-alkylpurines as adenosine receptor ligands
-
Camaioni E., Costanzi S., Vittori S., Volpini R., Klotz K.-N., Cristalli G. New substituted 9-alkylpurines as adenosine receptor ligands. Bioorg. Med. Chem. 6:1998;523-533.
-
(1998)
Bioorg. Med. Chem.
, vol.6
, pp. 523-533
-
-
Camaioni, E.1
Costanzi, S.2
Vittori, S.3
Volpini, R.4
Klotz, K.-N.5
Cristalli, G.6
-
15
-
-
0032461854
-
Characterization of potent ligands at human adenosine receptor
-
Cristalli G., Camaioni E., Costanzi S., Vittori S., Volpini R., Klotz K.N. Characterization of potent ligands at human adenosine receptor. Drug Dev. Res. 45:1998;176-181.
-
(1998)
Drug Dev. Res.
, vol.45
, pp. 176-181
-
-
Cristalli, G.1
Camaioni, E.2
Costanzi, S.3
Vittori, S.4
Volpini, R.5
Klotz, K.N.6
-
16
-
-
0036430347
-
Purine nuclosides bearing 1-alkynyl chains as adenosine receptor agonists
-
R. Volpini, S. Costanzi, C. Lambertucci, S. Vittori, G. Cristalli, Purine nuclosides bearing 1-alkynyl chains as adenosine receptor agonists, Curr. Pharm. Des., 8 (2002) 2285-2298.
-
(2002)
Curr. Pharm. Des.
, vol.8
, pp. 2285-2298
-
-
Volpini, R.1
Costanzi, S.2
Lambertucci, C.3
Vittori, S.4
Cristalli, G.5
-
17
-
-
0031754497
-
Receptors for purines and pyrimidines
-
Ralevic V., Burnstock G. Receptors for purines and pyrimidines. Pharmacol. Rev. 50:1998;413-492.
-
(1998)
Pharmacol. Rev.
, vol.50
, pp. 413-492
-
-
Ralevic, V.1
Burnstock, G.2
-
18
-
-
0035170508
-
Collecting and harvesting biological data: The GPCRDB and NucleaRDB databases
-
Horn F., Vriend G., Cohen F.E. Collecting and harvesting biological data: the GPCRDB and NucleaRDB databases. Nucleic Acids Res. 29:2001;346-349.
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 346-349
-
-
Horn, F.1
Vriend, G.2
Cohen, F.E.3
-
19
-
-
0034006037
-
Identification of threonine residues controlling the agonist-dependent phosphorylation and desensitization of the rat A(3) adenosine receptor
-
Palmer T.M., Stiles G.L. Identification of threonine residues controlling the agonist-dependent phosphorylation and desensitization of the rat A(3) adenosine receptor. Mol. Pharmacol. 57:2000;539-545.
-
(2000)
Mol. Pharmacol.
, vol.57
, pp. 539-545
-
-
Palmer, T.M.1
Stiles, G.L.2
-
20
-
-
0034817072
-
Constitutive activation of A(3) adenosine receptors by site-directed mutagenesis
-
Chen A., Gao Z.G., Barak D., Liang B.T., Jacobson K.A. Constitutive activation of A(3) adenosine receptors by site-directed mutagenesis. Biochem. Biophys. Res. Commun. 284:2001;596-601.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.284
, pp. 596-601
-
-
Chen, A.1
Gao, Z.G.2
Barak, D.3
Liang, B.T.4
Jacobson, K.A.5
-
21
-
-
0035935737
-
Neoceptor concept based on molecular complementarity in GPCRs: A mutant adenosine A(3) receptor with selectively enhanced affinity for amine-modified nucleosides
-
Jacobson K.A., Gao Z.G., Chen A., Barak D., Kim S.A., Lee K., Link A., Rompaey P.V., van Calenbergh S., Liang B.T. Neoceptor concept based on molecular complementarity in GPCRs: a mutant adenosine A(3) receptor with selectively enhanced affinity for amine-modified nucleosides. J. Med. Chem. 44:2001;4125-4136.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 4125-4136
-
-
Jacobson, K.A.1
Gao, Z.G.2
Chen, A.3
Barak, D.4
Kim, S.A.5
Lee, K.6
Link, A.7
Rompaey, P.V.8
Van Calenbergh, S.9
Liang, B.T.10
-
22
-
-
0033396728
-
Adenosine and ischemic preconditioning
-
Liang B.T., Jacobson K.A. Adenosine and ischemic preconditioning. Curr. Pharm. Des. 5:1999;1029-1041.
-
(1999)
Curr. Pharm. Des.
, vol.5
, pp. 1029-1041
-
-
Liang, B.T.1
Jacobson, K.A.2
-
27
-
-
0028238771
-
2 adenosine receptor agonists with potent inhibitory activity on platelet aggregation
-
2 adenosine receptor agonists with potent inhibitory activity on platelet aggregation. J. Med. Chem. 37:1994;1720-1726.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 1720-1726
-
-
Cristalli, G.1
Volpini, R.2
Vittori, S.3
Camaioni, E.4
Monopoli, A.5
Conti, A.6
Dionisotti, S.7
Zocchi, C.8
Ongini, E.9
-
28
-
-
0028944624
-
2a adenosine receptor agonists
-
2a adenosine receptor agonists. J. Med. Chem. 38:1995;1462-1472.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1462-1472
-
-
Cristalli, G.1
Camaioni, E.2
Vittori, S.3
Volpini, R.4
Borea, P.A.5
Conti, A.6
Dionisotti, S.7
Ongini, E.8
Monopoli, A.9
-
29
-
-
0037130186
-
2B ligands
-
2B ligands, J. Med. Chem., 45 (2002) 3271-3279.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3271-3279
-
-
Volpini, R.1
Costanzi, S.2
Lambertucci, C.3
Taffi, S.4
Vittori, S.5
Klotz, K.-N.6
Cristalli, G.7
-
30
-
-
84986438505
-
Modification of nucleic acid bases via radical intermediates: Synthesis of dihalogenated purine nucleosides
-
V. Nair, S.G. Richardson, Modification of nucleic acid bases via radical intermediates: synthesis of dihalogenated purine nucleosides, Synthesis (1982) 670-672.
-
(1982)
Synthesis
, pp. 670-672
-
-
Nair, V.1
Richardson, S.G.2
-
31
-
-
15444352073
-
3 adenosine receptor agonists
-
3 adenosine receptor agonists. J. Med. Chem. 41:1998;3174-3185.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 3174-3185
-
-
Baraldi, P.G.1
Cacciari, B.2
Pineda de Las Infantas, M.J.3
Romagnoli, R.4
Spalluto, G.5
Volpini, R.6
Costanzi, S.7
Vittori, S.8
Cristalli, G.9
Melman, N.10
Park, K.11
Ji, X.12
Jacobson, K.A.13
-
32
-
-
0033395414
-
Synthesis of di- and tri-substituted adenosine derivatives and their affinity at human adenosine receptor subtypes
-
Volpini R., Camaioni E., Costanzi S., Vittori S., Klotz K.-N., Cristalli G. Synthesis of di- and tri-substituted adenosine derivatives and their affinity at human adenosine receptor subtypes. Nucleosides Nucleotides. 18:1999;2511-2520.
-
(1999)
Nucleosides Nucleotides
, vol.18
, pp. 2511-2520
-
-
Volpini, R.1
Camaioni, E.2
Costanzi, S.3
Vittori, S.4
Klotz, K.-N.5
Cristalli, G.6
-
33
-
-
0031931065
-
Comparative pharmacology of human adenosine subtypes-characterization of stably transfected receptors in CHO cells
-
Klotz K.-N., Hessling J., Hegler J., Owman B., Kull B., Fredholm B.B., Lohse M.J. Comparative pharmacology of human adenosine subtypes-characterization of stably transfected receptors in CHO cells. Naunyn-Schmiedeberg's Arch. Pharmacol. 357:1998;1-9.
-
(1998)
Naunyn-Schmiedeberg's Arch. Pharmacol.
, vol.357
, pp. 1-9
-
-
Klotz, K.-N.1
Hessling, J.2
Hegler, J.3
Owman, B.4
Kull, B.5
Fredholm, B.B.6
Lohse, M.J.7
-
36
-
-
0034850928
-
Synthesis and adenosine receptor affinity and potency of 8-alkynyl derivatives of adenosine
-
Lambertucci C., Costanzi S., Vittori S., Volpini R., Cristalli G. Synthesis and adenosine receptor affinity and potency of 8-alkynyl derivatives of adenosine. Nucleosides Nucleotides Nucleic Acids. 20:2001;1153-1157.
-
(2001)
Nucleosides Nucleotides Nucleic Acids
, vol.20
, pp. 1153-1157
-
-
Lambertucci, C.1
Costanzi, S.2
Vittori, S.3
Volpini, R.4
Cristalli, G.5
-
37
-
-
0018831826
-
Adenosine receptor activation in human fibroblasts: Nucleoside agonists and antagonists
-
Bruns R.F. Adenosine receptor activation in human fibroblasts: nucleoside agonists and antagonists. Can. J. Physiol. Pharmacol. 58:1980;673-691.
-
(1980)
Can. J. Physiol. Pharmacol.
, vol.58
, pp. 673-691
-
-
Bruns, R.F.1
-
38
-
-
0018899928
-
NMR studies in the syn-anti dynamic equilibrium in purine nucleosides and nucleotides
-
Stolarski R., Dudycz L., Shugar D. NMR studies in the syn-anti dynamic equilibrium in purine nucleosides and nucleotides. Eur. J. Biochem. 108:1980;111-121.
-
(1980)
Eur. J. Biochem.
, vol.108
, pp. 111-121
-
-
Stolarski, R.1
Dudycz, L.2
Shugar, D.3
-
39
-
-
0018473914
-
1H NMR study of the syn-anti dynamic equilibrium in adenine nucleosides and nucleotides with the aid of some synthetic model analogues with fixed conformations
-
1H NMR study of the syn-anti dynamic equilibrium in adenine nucleosides and nucleotides with the aid of some synthetic model analogues with fixed conformations. Z. Naturforsch., Teil. C. 34C:1979;359-373.
-
(1979)
Z. Naturforsch., Teil. C
, vol.34 C
, pp. 359-373
-
-
Dudycz, L.1
Stolarski, R.2
Pless, R.3
Shugar, D.4
-
41
-
-
0034604451
-
Crystal structure of rhodopsin: AG protein-coupled receptor
-
Palczewski K., Kumasaka T., Hori T., Behnke C.A., Motoshima H., Fox B.A., Le Trong I., Teller D.C., Okada T., Stenkamp R.E., Yamamoto M., Miyano M. Crystal structure of rhodopsin: AG protein-coupled receptor. Science. 289:2000;739-745.
-
(2000)
Science
, vol.289
, pp. 739-745
-
-
Palczewski, K.1
Kumasaka, T.2
Hori, T.3
Behnke, C.A.4
Motoshima, H.5
Fox, B.A.6
Le Trong, I.7
Teller, D.C.8
Okada, T.9
Stenkamp, R.E.10
Yamamoto, M.11
Miyano, M.12
-
42
-
-
0033954256
-
The protein data bank
-
Berman H.M., Westbrook J., Feng Z., Gilliland G., Bhat T.N., Weissig H., Shindyalov I.N., Bourne P.E. The protein data bank. Nucleic Acids Res. 28:2000;235-242.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 235-242
-
-
Berman, H.M.1
Westbrook, J.2
Feng, Z.3
Gilliland, G.4
Bhat, T.N.5
Weissig, H.6
Shindyalov, I.N.7
Bourne, P.E.8
-
43
-
-
0028859493
-
Ribose-modified adenosine analogues as potential partial agonists for the adenosine receptor
-
van der Wenden E.M., Von Frijtag Drabbe Kunzel J.K., Mathot R.A., Danhof M., IJzerman A.P., Soudijn W. Ribose-modified adenosine analogues as potential partial agonists for the adenosine receptor. J. Med. Chem. 38:1995;4000-4006.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4000-4006
-
-
Van der Wenden, E.M.1
Von Frijtag Drabbe Kunzel, J.K.2
Mathot, R.A.3
Danhof, M.4
IJzerman, A.P.5
Soudijn, W.6
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