-
1
-
-
0001892930
-
P1 and P2 purine and pyrimidine receptors
-
Abbracchio, M. P., Williams, M., Ed., in press
-
Jacobson, K. A.; Knutsen, L. J. S. P1 and P2 purine and pyrimidine receptors. Handbook of Experimental Pharmacology; Abbracchio, M. P., Williams, M., Ed., in press.
-
Handbook of Experimental Pharmacology
-
-
Jacobson, K.A.1
Knutsen, L.J.S.2
-
2
-
-
0032958071
-
A1 and A3 adenosine receptor agonists: An overview
-
Baraldi, P. G.; Cacciari, B.; Romagnoli, R.; Spalluto G. A1 and A3 adenosine receptor agonists: An overview. Exp. Opin. Therap. Patents 1999, 9, 515-527.
-
(1999)
Exp. Opin. Therap. Patents
, vol.9
, pp. 515-527
-
-
Baraldi, P.G.1
Cacciari, B.2
Romagnoli, R.3
Spalluto, G.4
-
4
-
-
0032540196
-
Adenosine receptor activation and nociception
-
Sawynok, J. Adenosine receptor activation and nociception. Eur. J. Pharmacol. 1998, 347, 1-11.
-
(1998)
Eur. J. Pharmacol.
, vol.347
, pp. 1-11
-
-
Sawynok, J.1
-
5
-
-
0030777067
-
1 receptor agonists with differing lipophilicity in rats: Comparison of pharmacokinetic, hemodynamic and EEG effects
-
1 receptor agonists with differing lipophilicity in rats: Comparison of pharmacokinetic, hemodynamic and EEG effects. Naunyn-Schmiedeberg's Arch. Pharmacol. 1997, 356, 827-837.
-
(1997)
Naunyn-schmiedeberg's Arch. Pharmacol.
, vol.356
, pp. 827-837
-
-
Van Schaick, E.A.1
Kulkarni, C.2
Von Frijtag Drabbe Künzel, J.K.3
Mathôt, R.A.A.4
Cristalli, G.5
Ijzerman, A.P.6
Danhof, M.7
-
6
-
-
0028906835
-
General pharmacology of SDZ WAG 994, a potent selective and orally active adenosine AI receptor agonist
-
Wagner, H.; Milavec-Krizman, M.; Gadient, F.; Menninger, K.; Schoeffter, P.; Tapparelli, C.; Pfannkuche, H.-J.; Fozard, J. R. General pharmacology of SDZ WAG 994, a potent selective and orally active adenosine AI receptor agonist. Drug Dev. Res. 1995, 34, 276-288.
-
(1995)
Drug Dev. Res.
, vol.34
, pp. 276-288
-
-
Wagner, H.1
Milavec-Krizman, M.2
Gadient, F.3
Menninger, K.4
Schoeffter, P.5
Tapparelli, C.6
Pfannkuche, H.-J.7
Fozard, J.R.8
-
9
-
-
0028201349
-
1-mediated hemodynamic effects
-
1-mediated hemodynamic effects. J. Pharmacol. Exp. Ther. 1994, 265, 1506-1511.
-
(1994)
J. Pharmacol. Exp. Ther.
, vol.265
, pp. 1506-1511
-
-
Casati, C.1
Monopoli, A.2
Dionisotti, S.3
Zocchi, C.4
Bonizzoni, E.5
Ongini, E.6
-
10
-
-
0032931515
-
Indirect modulation of dopamine D2 receptors as potential pharmacotherapy for schizophrenia: I. Adenosine agonists
-
Dixon, D. A.; Fenix, L. A.; Kim, D. M.; Raffa, R. B. Indirect modulation of dopamine D2 receptors as potential pharmacotherapy for schizophrenia: I. Adenosine agonists. Ann. Pharmacother. 1999, 33, 480-488.
-
(1999)
Ann. Pharmacother.
, vol.33
, pp. 480-488
-
-
Dixon, D.A.1
Fenix, L.A.2
Kim, D.M.3
Raffa, R.B.4
-
11
-
-
0022508520
-
Hypotensive and renal vasodilator effects of carbocyclic adenosine (aristeromycin) in anesthetized spontaneously hypertensive rats
-
Dunham, E. W.; Vince, R. Hypotensive and renal vasodilator effects of carbocyclic adenosine (aristeromycin) in anesthetized spontaneously hypertensive rats. J. Pharmacol. Exp. Ther. 1986, 238, 954-959.
-
(1986)
J. Pharmacol. Exp. Ther.
, vol.238
, pp. 954-959
-
-
Dunham, E.W.1
Vince, R.2
-
12
-
-
0024474064
-
Effects of adenosine A2 receptor agonists on nucleoside transport
-
Balwierczak, J. L.; Krulan, C. M.; Wang, Z. C.; Chen, J.; Jeng, A. Y. Effects of adenosine A2 receptor agonists on nucleoside transport. J. Pharmacol. Exp. Ther. 1989, 251, 279-287.
-
(1989)
J. Pharmacol. Exp. Ther.
, vol.251
, pp. 279-287
-
-
Balwierczak, J.L.1
Krulan, C.M.2
Wang, Z.C.3
Chen, J.4
Jeng, A.Y.5
-
13
-
-
0032941838
-
Cardiovascular pharmacology of the adenosine A1/A2-receptor agonist AMP 579: Coronary hemodynamic and cardioprotective effects in the canine myocardium
-
McVey, M. J.; Smits, G. J.; Cox, B. F.; Kitzen, J. M.; Clark, K. L.; Perrone, M. H. Cardiovascular pharmacology of the adenosine A1/A2-receptor agonist AMP 579: Coronary hemodynamic and cardioprotective effects in the canine myocardium. J. Cardiovasc. Pharmacol. 1999, 33, 703-710.
-
(1999)
J. Cardiovasc. Pharmacol.
, vol.33
, pp. 703-710
-
-
McVey, M.J.1
Smits, G.J.2
Cox, B.F.3
Kitzen, J.M.4
Clark, K.L.5
Perrone, M.H.6
-
14
-
-
0028915714
-
Search for new purine-and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors
-
Siddiqi, S. M.; Jacobson, K. A.; Esker, J. L.; Melman, N.; Tiwari, K. N.; Secrist, J. A.; Schneller, S. W.; Cristalli, G.; Johnson, C. A.; IJzerman, A. P. Search for new purine-and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptors. J. Med. Chem. 1995, 38, 1174-1188.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1174-1188
-
-
Siddiqi, S.M.1
Jacobson, K.A.2
Esker, J.L.3
Melman, N.4
Tiwari, K.N.5
Secrist, J.A.6
Schneller, S.W.7
Cristalli, G.8
Johnson, C.A.9
Ijzerman, A.P.10
-
15
-
-
0029063510
-
Specific transcriptional inhibition of bone marrow-derived macrophage tumor necrosis factor-alpha gene expression and protein production using novel enantiomeric carbocyclic nucleoside analogues
-
Bradshaw, M.; Rutherford, M. S.; Hoeper, B. J.; McWhinney, C. D.; Borcherding, D. R.; Schook, L. B.; Edwards, C. K., III Specific transcriptional inhibition of bone marrow-derived macrophage tumor necrosis factor-alpha gene expression and protein production using novel enantiomeric carbocyclic nucleoside analogues. J. Pharmacol. Exp. Ther. 1995, 273, 1506-1518.
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.273
, pp. 1506-1518
-
-
Bradshaw, M.1
Rutherford, M.S.2
Hoeper, B.J.3
McWhinney, C.D.4
Borcherding, D.R.5
Schook, L.B.6
Edwards C.K. III7
-
16
-
-
0030605935
-
Activation of adenosine A3 receptors on macrophages inhibits tumor necrosis factor-alpha
-
McWhinney, C. D.; Dudley, M. W.; Bowlin, T. L.; Peet, N. P.; Schook, L.; Bradshaw, M.; De, M.; Borcherding, D. R.; Edwards, C. K., III Activation of adenosine A3 receptors on macrophages inhibits tumor necrosis factor-alpha. Eur. J. Pharmacol. 1996, 310, 209-216.
-
(1996)
Eur. J. Pharmacol.
, vol.310
, pp. 209-216
-
-
McWhinney, C.D.1
Dudley, M.W.2
Bowlin, T.L.3
Peet, N.P.4
Schook, L.5
Bradshaw, M.6
De, M.7
Borcherding, D.R.8
Edwards C.K. III9
-
17
-
-
0028004592
-
Conformationally locked nucleoside analogues. Synthesis of dideoxycarbocyclic nucleoside analogues structurally related to neplanocin C
-
Rodriguez, J. B.; Marquez, V. E.; Nicklaus, M. C.; Mitsuya, H.; Barchi, J. J., Jr. Conformationally locked nucleoside analogues. Synthesis of dideoxycarbocyclic nucleoside analogues structurally related to neplanocin C. J. Med. Chem. 1994, 37, 3389-3399.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3389-3399
-
-
Rodriguez, J.B.1
Marquez, V.E.2
Nicklaus, M.C.3
Mitsuya, H.4
Barchi J.J., Jr.5
-
18
-
-
0000855901
-
4′,1′a-Methanocarbocyclic adenosine analogues as potential inhibitors of S-adenosylhomocysteine hydrolase
-
Jeong, L. S.; Marquez, V. E.; Yuan, C.-S.; Borchardt, R. T. 4′,1′a-Methanocarbocyclic adenosine analogues as potential inhibitors of S-adenosylhomocysteine hydrolase. Heterocycles 1995, 41, 2651-2656.
-
(1995)
Heterocycles
, vol.41
, pp. 2651-2656
-
-
Jeong, L.S.1
Marquez, V.E.2
Yuan, C.-S.3
Borchardt, R.T.4
-
19
-
-
0029815436
-
Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides?
-
Marquez, V. E.; Siddiqui, M. A.; Ezzitouni, A.; Russ, P.; Wang, J.; Wagner, R. W.; Matteucci, M. D. Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides? J. Med. Chem. 1996, 39, 3739-3747.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3739-3747
-
-
Marquez, V.E.1
Siddiqui, M.A.2
Ezzitouni, A.3
Russ, P.4
Wang, J.5
Wagner, R.W.6
Matteucci, M.D.7
-
20
-
-
0030749499
-
(1S, 2R)-[(Benzyloxy)-methyl]cyclopent-3-enol. A versatile synthon for the preparation of 4′,1′a-metnano and 1′,1′a-methano carbocyclic nucleosides
-
Ezzitouni, A.; Russ, P.; Marquez, V. E. (1S, 2R)-[(Benzyloxy)-methyl]cyclopent-3-enol. A versatile synthon for the preparation of 4′,1′a-metnano and 1′,1′a-methano carbocyclic nucleosides. J. Org. Chem. 1997, 62, 4870-4873.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4870-4873
-
-
Ezzitouni, A.1
Russ, P.2
Marquez, V.E.3
-
21
-
-
0032054586
-
HIV-1 Reverse Transcriptase Can Discriminate Between Two Conformationally Locked Carbocyclic AZT triphosphate Analogues
-
Marquez, V. E.; Ezzitouni, A.; Russ, P.; Siddiqui, M. A.; Ford, Jr.; H.; Feldman, R. J.; Mitsuya, H.; George, C.; Barchi, J. J., Jr. HIV-1 Reverse Transcriptase Can Discriminate Between Two Conformationally Locked Carbocyclic AZT triphosphate Analogues. J. Am. Chem. Soc. 1998, 720, 2780-2789.
-
(1998)
J. Am. Chem. Soc.
, vol.720
, pp. 2780-2789
-
-
Marquez, V.E.1
Ezzitouni, A.2
Russ, P.3
Siddiqui, M.A.4
Ford, J.H.5
Feldman, R.J.6
Mitsuya, H.7
George, C.8
Barchi J.J., Jr.9
-
22
-
-
0032989645
-
Conformationally restricted nucleosides. The reaction of adenosine deaminase with substrates built on a bicyclo[3.1.0]hexane template
-
Marquez, V. E.; Russ, P.; Alonso, R.; Siddiqui, M. A.; Shin, K. J.; George, C.; Nicklaus, M.; Dai, F.; Ford, H., Jr. Conformationally restricted nucleosides. The reaction of adenosine deaminase with substrates built on a bicyclo[3.1.0]hexane template. Nucleosides Nucleotides 1999, 18, 521-530.
-
(1999)
Nucleosides Nucleotides
, vol.18
, pp. 521-530
-
-
Marquez, V.E.1
Russ, P.2
Alonso, R.3
Siddiqui, M.A.4
Shin, K.J.5
George, C.6
Nicklaus, M.7
Dai, F.8
Ford H., Jr.9
-
23
-
-
0000633066
-
Construction of the bicyclo[3.1.0]hexane template of a Conformationally locked carbocyclic adenosine via an olefin ketocarbene cycloaddition
-
Shin, K. J.; Moon, H. R.; George, C.; Marquez, V. E. Construction of the bicyclo[3.1.0]hexane template of a Conformationally locked carbocyclic adenosine via an olefin ketocarbene cycloaddition. J. Org. Chem. 2000, 65, 2172-2178.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 2172-2178
-
-
Shin, K.J.1
Moon, H.R.2
George, C.3
Marquez, V.E.4
-
24
-
-
0031593681
-
3 adenosine receptors: Novel ligands and paradoxical effects
-
3 adenosine receptors: Novel ligands and paradoxical effects. Trends Pharmacol. Sci. 1998, 19, 184-191.
-
(1998)
Trends Pharmacol. Sci.
, vol.19
, pp. 184-191
-
-
Jacobson, K.A.1
-
25
-
-
0028218322
-
3-selective adenosine agonists
-
3-selective adenosine agonists. J. Med. Chem. 1994, 37, 636-646.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 636-646
-
-
Gallo-Rodriguez, C.1
Ji, X.-D.2
Melman, N.3
Siegman, B.D.4
Sanders, L.H.5
Orlina, J.6
Fischer, B.7
Pu, Q.8
Olah, M.E.9
Van Galen, P.J.M.10
Stiles, G.L.11
Jacobson, K.A.12
-
26
-
-
0028171602
-
3-adenosine receptors
-
3-adenosine receptors. J. Med. Chem. 1994, 37, 3614-3621.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3614-3621
-
-
Kim, H.O.1
Ji, X.2
Siddiqi, S.M.3
Olah, M.E.4
Stiles, G.L.5
Jacobson, K.A.6
-
29
-
-
0030694505
-
3 adenosine receptor-selective antagonists
-
3 adenosine receptor-selective antagonists. Neuropharmacology 1997, 9, 1157-1165.
-
(1997)
Neuropharmacology
, vol.9
, pp. 1157-1165
-
-
Jacobson, K.A.1
Park, K.S.2
Jiang, J.-L.3
Kim, Y.-C.4
Olah, M.E.5
Stiles, G.L.6
Ji, X.-D.7
-
31
-
-
0031894806
-
5′-Substituted adenosine analogues as new high-affinity partial agonists for the adenosine A1 receptor
-
van der Wenden, E. M.; Carnielli, M.; Roelen, H. C. P. F.; Lorenzen, A.; von Frijtag Drabbe Künzel, J. K.; IJzerman, A. P. 5′-Substituted adenosine analogues as new high-affinity partial agonists for the adenosine A1 receptor. J. Med. Chem. 1998, 41, 102-108.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 102-108
-
-
Van Der Wenden, E.M.1
Carnielli, M.2
Roelen, H.C.P.F.3
Lorenzen, A.4
Von Frijtag Drabbe Künzel, J.K.5
Ijzerman, A.P.6
-
32
-
-
0031434924
-
Differences between natural and recombinant G protein-coupled receptor systems with varying receptor/G protein stoichiometry
-
Kenakin, T. Differences between natural and recombinant G protein-coupled receptor systems with varying receptor/G protein stoichiometry. Trends Pharmacol Sci. 1997, 18, 456-464.
-
(1997)
Trends Pharmacol Sci.
, vol.18
, pp. 456-464
-
-
Kenakin, T.1
-
33
-
-
0032819108
-
Influence of G protein type on agonist efficacy
-
Yang, Q.; Lanier, S. M. Influence of G protein type on agonist efficacy. Mol. Pharmacol. 1999, 56, 651-656.
-
(1999)
Mol. Pharmacol.
, vol.56
, pp. 651-656
-
-
Yang, Q.1
Lanier, S.M.2
-
34
-
-
0001205470
-
Partial agonists and G protein-coupled receptor desensitization
-
Clark, R. B.; Knoll, B. J.; Barber, R. Partial agonists and G protein-coupled receptor desensitization. Trends Pharmacol. Sci. 1999, 20, 279-286.
-
(1999)
Trends Pharmacol. Sci.
, vol.20
, pp. 279-286
-
-
Clark, R.B.1
Knoll, B.J.2
Barber, R.3
-
35
-
-
0033595283
-
Selective inhibition of cocaine-seeking behaviour by a partial dopamine D3 receptor agonist
-
Pilla, M.; Perachon, S.; Sautel, F.; Garrido, F.; Mann, A.; Wermuth, C. G.; Schwartz, J.-C.; Everitt, B. J.; Sokoloff, P. Selective inhibition of cocaine-seeking behaviour by a partial dopamine D3 receptor agonist. Nature 1999, 400, 371-375.
-
(1999)
Nature
, vol.400
, pp. 371-375
-
-
Pilla, M.1
Perachon, S.2
Sautel, F.3
Garrido, F.4
Mann, A.5
Wermuth, C.G.6
Schwartz, J.-C.7
Everitt, B.J.8
Sokoloff, P.9
-
36
-
-
0034624785
-
1 receptor ligands
-
1 receptor ligands. J. Med. Chem. 2000, 43, 829-842.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 829-842
-
-
Nandanan, E.1
Jang, S.Y.2
Moro, S.3
Kim, H.4
Siddiqi, M.A.5
Russ, P.6
Marquez, V.7
Busson, R.8
Herdewijn, P.9
Harden, T.K.10
Boyer, J.L.11
Jacobson, K.A.12
-
37
-
-
0032492932
-
2′-C-Methyl analogues of selective adenosine receptor agonists: Synthesis and binding studies
-
Franchetti, P.; Cappellacci L.; Marchetti, S.; Trincavelli, L.; Martini, C.; Mazzoni, M. R.; Lucacchini, A.; Grifantini, M. 2′-C-Methyl analogues of selective adenosine receptor agonists: Synthesis and binding studies. J. Med. Chem. 1998, 41, 1708-1715.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1708-1715
-
-
Franchetti, P.1
Cappellacci, L.2
Marchetti, S.3
Trincavelli, L.4
Martini, C.5
Mazzoni, M.R.6
Lucacchini, A.7
Grifantini, M.8
-
38
-
-
0032559887
-
1 receptor: Molecular modeling and site-directed mutagenesis as tools to identify agonist and antagonist recognition sites
-
1 receptor: Molecular modeling and site-directed mutagenesis as tools to identify agonist and antagonist recognition sites. J. Med. Chem. 1998, 41, 1456-1466.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 1456-1466
-
-
Moro, S.1
Guo, D.2
Camaioni, E.3
Boyer, J.L.4
Harden, K.T.5
Jacobson, K.A.6
-
39
-
-
0015511563
-
Conformational Analysis of the Sugar Ring in Nucleosides and Nucleotides. A New Description Using the Concept of Pseudorotation
-
Altona, C.; Sundaranlingam, M. Conformational Analysis of the Sugar Ring in Nucleosides and Nucleotides. A New Description Using the Concept of Pseudorotation. J. Am. Chem. Soc. 1972, 94, 8205-8212.
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 8205-8212
-
-
Altona, C.1
Sundaranlingam, M.2
-
41
-
-
0029146120
-
3 adenosine receptors: Design of selective ligands and therapeutic prospects
-
3 adenosine receptors: design of selective ligands and therapeutic prospects. Drugs Future 1995, 20, 689-699.
-
(1995)
Drugs Future
, vol.20
, pp. 689-699
-
-
Jacobson, K.A.1
Kim, H.O.2
Siddiqi, S.M.3
Olah, M.E.4
Stiles, G.L.5
Von Lubitz, D.K.J.E.6
|