-
2
-
-
0022629214
-
Extracellular ATP: Effects, sources and fate
-
Gordon, J. L. Extracellular ATP: Effects, Sources and Fate. Biochem. J. 1986, 233, 309-319.
-
(1986)
Biochem. J.
, vol.233
, pp. 309-319
-
-
Gordon, J.L.1
-
3
-
-
0030340330
-
P2 purinoceptors: Historical perspective and classification
-
Chadwick, D. J., Goode, J. A., Eds.; John Wiley and Sons: Chichester
-
Burnstock, G. P2 Purinoceptors: Historical Perspective and Classification. In P2 Purinoceptors: Localisation, Function and Transduction Mechanisms (Ciba Foundation Symposium 1995); Chadwick, D. J., Goode, J. A., Eds.; John Wiley and Sons: Chichester, 1996; pp 1-29.
-
(1996)
P2 Purinoceptors: Localisation, Function and Transduction Mechanisms (Ciba Foundation Symposium 1995)
, pp. 1-29
-
-
Burnstock, G.1
-
4
-
-
0031914973
-
Molecular basis for ADP-induced platelet activation
-
Daniel, J. L.; Dangelmaier, C.; Jin, J.; Ashby, B.; Smith, J. B.; Kunapuli, S. P. Molecular Basis for ADP-induced Platelet Activation. J. Biol. Chem. 1998, 273, 2024-2029.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 2024-2029
-
-
Daniel, J.L.1
Dangelmaier, C.2
Jin, J.3
Ashby, B.4
Smith, J.B.5
Kunapuli, S.P.6
-
5
-
-
33947484336
-
Purine nucleosides IV. The synthesis of 6-halogenated 9-β-d-ribofuranosylpurines from inosine and guanosine
-
Gerster, J. F.; Jones, J. W.; Robins, R. K. Purine Nucleosides IV. The Synthesis of 6-Halogenated 9-β-D-Ribofuranosylpurines from Inosine and Guanosine. J. Org. Chem. 1963, 28, 945-948.
-
(1963)
J. Org. Chem.
, vol.28
, pp. 945-948
-
-
Gerster, J.F.1
Jones, J.W.2
Robins, R.K.3
-
6
-
-
85078325405
-
Photoinduced alkylthiolation of halogenated purine nucleosides
-
Nair, V.; Young, D. A. Photoinduced Alkylthiolation of Halogenated Purine Nucleosides. Synthesis 1986, 450-453.
-
(1986)
Synthesis
, pp. 450-453
-
-
Nair, V.1
Young, D.A.2
-
7
-
-
84986438505
-
Modification of nucleic acid bases via radical intermediates: Synthesis of dihalogenated purine nucleosides
-
Nair, V.; Richardson, S. G. 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
-
8
-
-
0017402041
-
Platelet aggregation inhibitors. IX. Chemical transformation of adenosine into 2-thioadenosine derivatives
-
Kikugawa, K.; Suehiro, H.; Yanase, R.; Aoki, A. Platelet Aggregation Inhibitors. IX. Chemical Transformation of Adenosine into 2-Thioadenosine Derivatives. Chem. Pharm. Bull. (Tokyo) 1977, 25, 1959-1969.
-
(1977)
Chem. Pharm. Bull. (Tokyo)
, vol.25
, pp. 1959-1969
-
-
Kikugawa, K.1
Suehiro, H.2
Yanase, R.3
Aoki, A.4
-
9
-
-
0014186966
-
A novel method for phosphorylation of nucleosides to 5′-nucleotides
-
Yoshikawa, M.; Kato, T.; Takenishi, T. A Novel Method for Phosphorylation of Nucleosides to 5′-Nucleotides. Tetrahedron Lett. 1967, 5065-5068.
-
(1967)
Tetrahedron Lett.
, pp. 5065-5068
-
-
Yoshikawa, M.1
Kato, T.2
Takenishi, T.3
-
10
-
-
84970573177
-
Darstellung von imidazoliden der phosphorsäure
-
Cramer, F. C.; Schaller, H.; Staab, H. A. Darstellung von Imidazoliden der Phosphorsäure. Chem. Ber. 1961, 94, 1612-1621.
-
(1961)
Chem. Ber.
, vol.94
, pp. 1612-1621
-
-
Cramer, F.C.1
Schaller, H.2
Staab, H.A.3
-
11
-
-
0027942835
-
FPL 66096: A novel, highly potent and selective antagonist at human platelet P2T-purinoceptors
-
Humphries, R. G.; Tomlinson, W.; Ingall, A. H.; Cage, P. A.; Leff, P. FPL 66096: A Novel, Highly Potent and Selective Antagonist at Human Platelet P2T-purinoceptors. Br. J. Pharmacol. 1994, 113, 1057-1063.
-
(1994)
Br. J. Pharmacol.
, vol.113
, pp. 1057-1063
-
-
Humphries, R.G.1
Tomlinson, W.2
Ingall, A.H.3
Cage, P.A.4
Leff, P.5
-
12
-
-
0022521314
-
ATP analogues and the Guinea pig tenia coli: A comparison of the structure-activity relationships of ectonucleotidases with those of the P2-purinoceptor
-
Welford, L. A.; Cusack, N. J.; Hourani, S. M. O. ATP Analogues and the Guinea Pig Tenia Coli: A Comparison of the Structure-activity Relationships of Ectonucleotidases with those of the P2-purinoceptor. Eur. J. Pharmacol. 1986, 129, 217-224.
-
(1986)
Eur. J. Pharmacol.
, vol.129
, pp. 217-224
-
-
Welford, L.A.1
Cusack, N.J.2
Hourani, S.M.O.3
-
13
-
-
84959965244
-
Isopolar vs isosteric phosphonate analogues of nucleotides
-
Blackburn, G. M.; Eckstein, F.; Kent, D. E.; Perree, T. D. Isopolar vs Isosteric Phosphonate Analogues of Nucleotides. Nucleosides Nucleotides 1985, 4, 165-167.
-
(1985)
Nucleosides Nucleotides
, vol.4
, pp. 165-167
-
-
Blackburn, G.M.1
Eckstein, F.2
Kent, D.E.3
Perree, T.D.4
-
14
-
-
2442633225
-
Phosphonate analogues of biological phosphates
-
Blackburn, G. M.; Taylor, G. E.; Tattershall, R. H.; Thatcher, G. R. J.; McLennan, A. Phosphonate Analogues of Biological Phosphates. Bioact. Mol. 1987, 3, 451-464.
-
(1987)
Bioact. Mol.
, vol.3
, pp. 451-464
-
-
Blackburn, G.M.1
Taylor, G.E.2
Tattershall, R.H.3
Thatcher, G.R.J.4
McLennan, A.5
-
15
-
-
0023248287
-
Pharmacological effects of isopolar phosphonate analogues of ATP on P2-purinoceptors in Guinea pig tenia coli and urinary bladder
-
Cusack, N. J.; Hourani, S. M. O.; Loizou, G. D.; Welford, L. A. Pharmacological Effects of Isopolar Phosphonate Analogues of ATP on P2-purinoceptors in Guinea Pig Tenia Coli and Urinary Bladder. Br. J. Pharmacol. 1987, 90, 791-795.
-
(1987)
Br. J. Pharmacol.
, vol.90
, pp. 791-795
-
-
Cusack, N.J.1
Hourani, S.M.O.2
Loizou, G.D.3
Welford, L.A.4
-
16
-
-
0029742163
-
Clodronate and osteoporosis
-
Kanis, J. A.; McCloskey, E. V.; Beneton, M. N. C. Clodronate and Osteoporosis. Maturitas 1996, 23 (Suppl.), S81-S86.
-
(1996)
Maturitas
, vol.23
, Issue.SUPPL.
-
-
Kanis, J.A.1
McCloskey, E.V.2
Beneton, M.N.C.3
-
17
-
-
0015311506
-
Analogues of adenosine 5′-diphosphate. New platelet aggregators. Influence of purine ring and phosphate chain substitutions on the platelet-aggregating potency of adenosine 5′-diphosphate
-
Gough, G.; Maguire, M. H.; Penglis, F. Analogues of Adenosine 5′-Diphosphate. New Platelet Aggregators. Influence of Purine Ring and Phosphate Chain Substitutions on the Platelet-aggregating Potency of Adenosine 5′-Diphosphate. Aust. Mol. Pharmacol. 1972, 8, 170-177.
-
(1972)
Aust. Mol. Pharmacol.
, vol.8
, pp. 170-177
-
-
Gough, G.1
Maguire, M.H.2
Penglis, F.3
-
19
-
-
0026065276
-
Further subclassification of ATP receptors based on agonist studies. Trends pharmacol
-
Dainty, I. A.; Leff, P.; McKechnie, K.; O'Connor, S. E. Further Subclassification of ATP Receptors Based on Agonist Studies. Trends Pharmacol. Sci. 1991, 12, 137-141.
-
(1991)
Sci.
, vol.12
, pp. 137-141
-
-
Dainty, I.A.1
Leff, P.2
McKechnie, K.3
O'Connor, S.E.4
-
20
-
-
0028955974
-
The short-acting P2T-purinoceptor antagonist, FPL 67085, reliably, reversibly and safely inhibits ADP-induced platelet aggregation ex vivo in man
-
Nassim, M. A.; Gardner, J. J.; Wilkinson, D.; Corfield, J. E.; Rudol, L.; Wyld, P. J. The Short-acting P2T-purinoceptor Antagonist, FPL 67085, Reliably, Reversibly and Safely Inhibits ADP-induced Platelet Aggregation ex vivo in Man. Br. J. Clin. Pharmacol. 1995, 39, 98P.
-
(1995)
Br. J. Clin. Pharmacol.
, vol.39
-
-
Nassim, M.A.1
Gardner, J.J.2
Wilkinson, D.3
Corfield, J.E.4
Rudol, L.5
Wyld, P.J.6
-
21
-
-
0007592393
-
The P2T purinoceptor antagonist FPL 67085, is a potent, efficacious and selective inhibitor of dynamic arterial thrombosis in the pentobarbitone-anaesthetised dog
-
Humphries, R. G.; Tomlinson, W.; Leff, P.; Ingall, A. H.; Kindon, N. D. The P2T Purinoceptor Antagonist FPL 67085, is a Potent, Efficacious and Selective Inhibitor of Dynamic Arterial Thrombosis in the Pentobarbitone-anaesthetised Dog. Br. J. Pharmacol. 1994, 114, 63P.
-
(1994)
Br. J. Pharmacol.
, vol.114
-
-
Humphries, R.G.1
Tomlinson, W.2
Leff, P.3
Ingall, A.H.4
Kindon, N.D.5
-
22
-
-
0028981512
-
Pharmacological profile of the novel P2T purinoceptor antagonist FPL 67085 in vitro and in the anaesthetised rat in vivo
-
Humphries, R. G.; Tomlinson, W.; Clegg, J. A.; Ingall, A. H.; Kindon, N. D.; Leff, P. Pharmacological Profile of the Novel P2T purinoceptor Antagonist FPL 67085 in vitro and in the Anaesthetised Rat in vivo. Br. J. Pharmacol. 1995, 115, 1110-1116.
-
(1995)
Br. J. Pharmacol.
, vol.115
, pp. 1110-1116
-
-
Humphries, R.G.1
Tomlinson, W.2
Clegg, J.A.3
Ingall, A.H.4
Kindon, N.D.5
Leff, P.6
-
23
-
-
0002442782
-
2T-receptor antagonists as novel antithrombotic agents
-
Jacobson, K. A., Jarvis, M. J., Eds.; Wiley-Liss Inc.: New York
-
2T-receptor Antagonists as Novel Antithrombotic Agents. In Purinergic Approaches in Experimental Therapeutics; Jacobson, K. A., Jarvis, M. J., Eds.; Wiley-Liss Inc.: New York, 1997; pp 203-216.
-
(1997)
Purinergic Approaches in Experimental Therapeutics
, pp. 203-216
-
-
Leff, P.1
Robertson, M.J.2
Humphries, R.G.3
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