-
1
-
-
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
-
2
-
-
0017744482
-
Adenosine deaminase deficiency and severe combined immunodeficiency disease
-
Van der Weyden M.B., Kelly W.N. Adenosine deaminase deficiency and severe combined immunodeficiency disease. Life Sci. 20:1977;1645-1650.
-
(1977)
Life Sci.
, vol.20
, pp. 1645-1650
-
-
Van Der Weyden, M.B.1
Kelly, W.N.2
-
3
-
-
0021832892
-
Elevated adenosine deaminase and purine nucleoside phosphorilase activity in peripheral blood null lymphocytes from patiens with acquired immune deficiency syndrome
-
Murray J.L., Loftin K.C., Munn C.G., Reuben J.M., Mansell P.W.A., Hersh E.M. Elevated adenosine deaminase and purine nucleoside phosphorilase activity in peripheral blood null lymphocytes from patiens with acquired immune deficiency syndrome. Blood. 65:1985;1318-1324.
-
(1985)
Blood
, vol.65
, pp. 1318-1324
-
-
Murray, J.L.1
Loftin, K.C.2
Munn, C.G.3
Reuben, J.M.4
Mansell, P.W.A.5
Hersh, E.M.6
-
4
-
-
0019206846
-
Adenosine deaminase inhibitors: Their role in chemotherapy and immunosuppression
-
Glazer R.I. Adenosine deaminase inhibitors: their role in chemotherapy and immunosuppression. Cancer Chemother. Pharmacol. 4:1980;227-235.
-
(1980)
Cancer Chemother. Pharmacol.
, vol.4
, pp. 227-235
-
-
Glazer, R.I.1
-
5
-
-
0030041938
-
Adenosine deaminase affects ligand-induced signalling by interacting with cell surface adenosine receptors
-
Ciruela F., Saura C., Canela E.I., Mallol J., Lluis C., Franco R. Adenosine deaminase affects ligand-induced signalling by interacting with cell surface adenosine receptors. FEBS Lett. 380:1996;219-223.
-
(1996)
FEBS Lett.
, vol.380
, pp. 219-223
-
-
Ciruela, F.1
Saura, C.2
Canela, E.I.3
Mallol, J.4
Lluis, C.5
Franco, R.6
-
6
-
-
0032503692
-
Adenosine deaminase and A1 adenosine receptors internalize together following agonists-induced receptor desensitization
-
Saura C.A., Mallol J., Canela E.I., Lluis C., Franco R. Adenosine deaminase and A1 adenosine receptors internalize together following agonists-induced receptor desensitization. J. Biol. Chem. 273:1998;17610-17617.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 17610-17617
-
-
Saura, C.A.1
Mallol, J.2
Canela, E.I.3
Lluis, C.4
Franco, R.5
-
8
-
-
0021956266
-
Modulation of hippocampal serotonin (5-HT) release by endogenous adenosine
-
Feuerstein T.J., Hertting G., Jackisch R. Modulation of hippocampal serotonin (5-HT) release by endogenous adenosine. Eur. J. Pharmacol. 107:1985;233-242.
-
(1985)
Eur. J. Pharmacol.
, vol.107
, pp. 233-242
-
-
Feuerstein, T.J.1
Hertting, G.2
Jackisch, R.3
-
9
-
-
0022256421
-
Adenosine: An endogenous modulator of hippocampal noradrenaline release
-
Jackisch R., Fehr R., Hertting G. Adenosine: an endogenous modulator of hippocampal noradrenaline release. Neuropharmacology. 24:1985;499-507.
-
(1985)
Neuropharmacology
, vol.24
, pp. 499-507
-
-
Jackisch, R.1
Fehr, R.2
Hertting, G.3
-
13
-
-
0028204236
-
2-Aryl-8-azaadenosines: Structure-activity relationships in the binding with A1 and A2 receptors. A comparison with the corresponding 9-benzyl-8-azaadenines
-
Biagi G., Giorgi I., Livi O., Scartoni V., Lucacchini A., Martini C., Tacchi P. 2-Aryl-8-azaadenosines: structure-activity relationships in the binding with A1 and A2 receptors. A comparison with the corresponding 9-benzyl-8-azaadenines. Farmaco. 49:1994;93-96.
-
(1994)
Farmaco
, vol.49
, pp. 93-96
-
-
Biagi, G.1
Giorgi, I.2
Livi, O.3
Scartoni, V.4
Lucacchini, A.5
Martini, C.6
Tacchi, P.7
-
14
-
-
0027081459
-
Evaluation of the quantitative contribution of an aryl group on C(2) of 8-azaadenines to binding with adenosine deaminase: A new synthesis of 8-azaadenosine
-
Biagi G., Giorgi I., Livi O., Scartoni V., Lucacchini A. Evaluation of the quantitative contribution of an aryl group on C(2) of 8-azaadenines to binding with adenosine deaminase: a new synthesis of 8-azaadenosine. Farmaco. 47:1992;1457-1476.
-
(1992)
Farmaco
, vol.47
, pp. 1457-1476
-
-
Biagi, G.1
Giorgi, I.2
Livi, O.3
Scartoni, V.4
Lucacchini, A.5
-
15
-
-
0015944892
-
Enzyme inhibitors. 26. Bridging hydrophobic and hydrophilic regions on adenosine deaminase with some 9-(2-hydroxy-3-alkyl)adenines
-
Schaeffer H.J., Scwender C.F. Enzyme inhibitors. 26. Bridging hydrophobic and hydrophilic regions on adenosine deaminase with some 9-(2-hydroxy-3-alkyl)adenines. J. Med. Chem. 17:(1):1974;6-8.
-
(1974)
J. Med. Chem.
, vol.17
, Issue.1
, pp. 6-8
-
-
Schaeffer, H.J.1
Scwender, C.F.2
-
17
-
-
0007656879
-
Ring transformation in reaction of heterocyclic halogen compounds with nucleophiles. XIII. Conversion of some 5-substituted 4-chloro-2- phenylpyrimidines into 4(5)-substituted 2-phenylimidazoles
-
van Meeteren H.W., van der Plas H.C. Ring transformation in reaction of heterocyclic halogen compounds with nucleophiles. XIII. Conversion of some 5-substituted 4-chloro-2-phenylpyrimidines into 4(5)-substituted 2-phenylimidazoles. Recl. Trav. Chim. Pays-Bas. 87:1968;1089-1098.
-
(1968)
Recl. Trav. Chim. Pays-Bas
, vol.87
, pp. 1089-1098
-
-
Van Meeteren, H.W.1
Van Der Plas, H.C.2
-
18
-
-
37049176095
-
New cytotoxic agents with tumour-inhibitory activity. Part I. Some aziridinopyrimidine derivatives
-
Hendry J.A., Homer R.F. New cytotoxic agents with tumour-inhibitory activity. Part I. Some aziridinopyrimidine derivatives. J. Chem. Soc. 1952;328-333.
-
(1952)
J. Chem. Soc.
, pp. 328-333
-
-
Hendry, J.A.1
Homer, R.F.2
-
19
-
-
0001255210
-
The stereospecific cyclization of a threo α-benzamide alcohol to a cis N-acyl aziridine
-
Boschelli D.H. The stereospecific cyclization of a threo α-benzamide alcohol to a cis N-acyl aziridine. Synth. Commun. 18:1988;1391-1395.
-
(1988)
Synth. Commun.
, vol.18
, pp. 1391-1395
-
-
Boschelli, D.H.1
-
20
-
-
0000932985
-
Ring closure of the 2-benzoylaminocyclohexanols. The mechanism of oxazoline formation
-
Johnson W.S., Schubert E.N. Ring closure of the 2- benzoylaminocyclohexanols. The mechanism of oxazoline formation. J. Am. Chem. Soc. 72:1950;2187-2190.
-
(1950)
J. Am. Chem. Soc.
, vol.72
, pp. 2187-2190
-
-
Johnson, W.S.1
Schubert, E.N.2
-
21
-
-
0025175018
-
Synthesis and anti-HIVactivity of carbocyclic 2′-3′- didehydro-2′-3′-dideoxy 2,6-substituted purine nucleosides
-
Vince R., Hua M. Synthesis and anti-HIVactivity of carbocyclic 2′-3′-didehydro-2′-3′-dideoxy 2,6-substituted purine nucleosides. J. Med. Chem. 33:1990;17-21.
-
(1990)
J. Med. Chem.
, vol.33
, pp. 17-21
-
-
Vince, R.1
Hua, M.2
-
22
-
-
0023580039
-
Synthesis and antiviral activity of carbocyclic analogues of xilofuranosides of 2-amino-6-substituted-purines and 2-amino-6-substituted-8- azapurines
-
Vince R., Turakhia R.H., Shannon W.M., Arnett G. Synthesis and antiviral activity of carbocyclic analogues of xilofuranosides of 2-amino-6-substituted- purines and 2-amino-6-substituted-8-azapurines. J. Med. Chem. 30:1987;2026-2030.
-
(1987)
J. Med. Chem.
, vol.30
, pp. 2026-2030
-
-
Vince, R.1
Turakhia, R.H.2
Shannon, W.M.3
Arnett, G.4
-
23
-
-
0002106784
-
6-cyclohexyladenosine binding to adenosine receptors in sheep cerebral cortex
-
6-cyclohexyladenosine binding to adenosine receptors in sheep cerebral cortex. Bull. Mol. Biol. Med. 11:1986;1-10.
-
(1986)
Bull. Mol. Biol. Med.
, vol.11
, pp. 1-10
-
-
Martini, C.1
Poli, M.2
Lucacchini, A.3
-
26
-
-
0000267781
-
-
S.P. Colowick, Kaplan N.O. New York: Academic Press
-
Kaplan N.O. Colowick S.P., Kaplan N.O. Methods in Enzymology. II: 1955;473 Academic Press, New York.
-
(1955)
Methods in Enzymology
, vol.2
, pp. 473
-
-
Kaplan, N.O.1
-
27
-
-
0019809405
-
Adenosine deaminase inhibitors. Conversion of a single chiral synthon into erithro- and threo-9-(2-hydroxy-3-nonyl)adenines
-
Bastian G., Bessodes M., Panzica R.P., Abushanab E., Chen S.-F., Stoeckler J.D., Parks R.E. Jr. Adenosine deaminase inhibitors. Conversion of a single chiral synthon into erithro- and threo-9-(2-hydroxy-3-nonyl)adenines. J. Med. Chem. 24:1981;1383-1385.
-
(1981)
J. Med. Chem.
, vol.24
, pp. 1383-1385
-
-
Bastian, G.1
Bessodes, M.2
Panzica, R.P.3
Abushanab, E.4
Chen, S.-F.5
Stoeckler, J.D.6
Parks Jr., R.E.7
-
28
-
-
0009764945
-
Enzyme inhibitors. VI. Studies on the bulk tolerance of adenosine deaminase for 6-substituted amino-9-(3-hydroxypropyl)purines
-
Schaeffer J., Vince R. Enzyme inhibitors. VI. Studies on the bulk tolerance of adenosine deaminase for 6-substituted amino-9-(3-hydroxypropyl) purines. J. Med. Chem. 8:1965;33-35.
-
(1965)
J. Med. Chem.
, vol.8
, pp. 33-35
-
-
Schaeffer, J.1
Vince, R.2
-
29
-
-
0030690021
-
Adenosine deaminase inhibitors: Synthesis, diastereoisomeric resolution and biological activity of 1-(2-hydroxy-3-nonyl)-1,2,4-triazole-3-carboxamide
-
Volpini R., Camaioni E., Lupidi G., Vittori S., Cristalli G. Adenosine deaminase inhibitors: synthesis, diastereoisomeric resolution and biological activity of 1-(2-hydroxy-3-nonyl)-1,2,4-triazole-3-carboxamide. Farmaco. 52:1997;429-433.
-
(1997)
Farmaco
, vol.52
, pp. 429-433
-
-
Volpini, R.1
Camaioni, E.2
Lupidi, G.3
Vittori, S.4
Cristalli, G.5
-
30
-
-
0028013346
-
Adenosine deaminase inhibitors: Synthesis and structure-activity relationships of 2-hydroxy-3-nonyl derivatives of azoles
-
Cristalli G., Eleuteri A., Volpini R., Vittori S., Camaioni E., Lupidi G. Adenosine deaminase inhibitors: synthesis and structure-activity relationships of 2-hydroxy-3-nonyl derivatives of azoles. J. Med. Chem. 37:1994;201-205.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 201-205
-
-
Cristalli, G.1
Eleuteri, A.2
Volpini, R.3
Vittori, S.4
Camaioni, E.5
Lupidi, G.6
-
31
-
-
1642361288
-
Design and evaluation of enzyme inhibitors, especially of adenosine deaminase
-
Schaeffer J. Design and evaluation of enzyme inhibitors, especially of adenosine deaminase. Top. Med. Chem. 3:1970;25-55.
-
(1970)
Top. Med. Chem.
, vol.3
, pp. 25-55
-
-
Schaeffer, J.1
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