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Results: 1-9 |
Results: 9
The utilization of a unified pharmacophore query in the discovery of new antagonists of the adenosine receptor family
Authors: Webb, TR Melman, N Lvovskiy, D Ji, XD Jacobson, KA
Citation: Tr. Webb et al., The utilization of a unified pharmacophore query in the discovery of new antagonists of the adenosine receptor family, BIOORG MED, 10(1), 2000, pp. 31-34
Anilide derivatives of an 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A(2B) adenosine receptors
Authors: Kim, YC Ji, XD Melman, N Linden, J Jacobson, KA
Citation: Yc. Kim et al., Anilide derivatives of an 8-phenylxanthine carboxylic congener are highly potent and selective antagonists at human A(2B) adenosine receptors, J MED CHEM, 43(6), 2000, pp. 1165-1172
Methanocarba analogues of purine nucleosides as potent and selective adenosine receptor agonists
Authors: Jacobson, KA Ji, XD Li, AH Melman, N Siddiqui, MA Shin, KJ Marquez, VE Ravi, RG
Citation: Ka. Jacobson et al., Methanocarba analogues of purine nucleosides as potent and selective adenosine receptor agonists, J MED CHEM, 43(11), 2000, pp. 2196-2203
Functionalized congeners of 1,4-dihydropyridines as antagonist molecular probes for A(3) adenosine receptors
Authors: Li, AH Chang, L Ji, XD Melman, N Jacobson, KA
Citation: Ah. Li et al., Functionalized congeners of 1,4-dihydropyridines as antagonist molecular probes for A(3) adenosine receptors, BIOCONJ CHE, 10(4), 1999, pp. 667-677
Pyran template approach to the design of novel A(3) adenosine receptor antagonists
Authors: Li, AH Ji, XD Kim, HS Melman, N Jacobson, KA
Citation: Ah. Li et al., Pyran template approach to the design of novel A(3) adenosine receptor antagonists, DRUG DEV R, 48(4), 1999, pp. 171-177
Acyl-hydrazide derivatives of a xanthine carboxylic congener (XCC) as selective antagonists at human A(2B) adenosine receptors
Authors: Kim, YC Karton, Y Ji, XD Melman, N Linden, J Jacobson, KA
Citation: Yc. Kim et al., Acyl-hydrazide derivatives of a xanthine carboxylic congener (XCC) as selective antagonists at human A(2B) adenosine receptors, DRUG DEV R, 47(4), 1999, pp. 178-188
Synthesis, CoMFA analysis, and receptor docking of 3,5-diacyl-2,4-dialkylpyridine derivatives as selective A(3) adenosine receptor antagonists
Authors: Li, AH Moro, S Forsyth, N Melman, N Ji, XD Jacobson, KA
Citation: Ah. Li et al., Synthesis, CoMFA analysis, and receptor docking of 3,5-diacyl-2,4-dialkylpyridine derivatives as selective A(3) adenosine receptor antagonists, J MED CHEM, 42(4), 1999, pp. 706-721
Selective A(3) adenosine receptor antagonists: Water-soluble 3,5-diacyl-1,2,4-trialkylpyridinium salts and their oxidative generation from dihydropyridine precursors
Authors: Xie, RY Li, AH Ji, XD Melman, N Olah, ME Stiles, GL Jacobson, KA
Citation: Ry. Xie et al., Selective A(3) adenosine receptor antagonists: Water-soluble 3,5-diacyl-1,2,4-trialkylpyridinium salts and their oxidative generation from dihydropyridine precursors, J MED CHEM, 42(20), 1999, pp. 4232-4238
Chiral resolution and stereospecificity of 6-phenyl-4-phenylethynyl-1,4-dihydropyridines as selective A(3) adenosine receptor antagonists
Authors: Jiang, JL Li, AH Jang, SY Chang, L Melman, N Moro, S Ji, XD Lobkovsky, EB Clardy, JC Jacobson, KA
Citation: Jl. Jiang et al., Chiral resolution and stereospecificity of 6-phenyl-4-phenylethynyl-1,4-dihydropyridines as selective A(3) adenosine receptor antagonists, J MED CHEM, 42(16), 1999, pp. 3055-3065
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