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91 related items for PubMed ID: 2959564
21. Characterization of a low affinity binding site for N6-substituted adenosine derivatives in rat testis membranes. Mazzoni MR, Buffoni RS, Giusti L, Lucacchini A. J Recept Signal Transduct Res; 1995; 15(7-8):905-29. PubMed ID: 8673723 [Abstract] [Full Text] [Related]
22. N6-methoxy-2-alkynyladenosine derivatives as highly potent and selective ligands at the human A3 adenosine receptor. Volpini R, Dal Ben D, Lambertucci C, Taffi S, Vittori S, Klotz KN, Cristalli G. J Med Chem; 2007 Mar 22; 50(6):1222-30. PubMed ID: 17309246 [Abstract] [Full Text] [Related]
23. Adenosine analogs mediating depressant effects on synaptic transmission in rat hippocampus: structure-activity relationships for the N6 subregion. Dunwiddie TV, Worth TS, Olsson RA. Naunyn Schmiedebergs Arch Pharmacol; 1986 Sep 22; 334(1):77-85. PubMed ID: 3024026 [Abstract] [Full Text] [Related]
24. Identification of the A2 adenosine receptor binding subunit by photoaffinity crosslinking. Barrington WW, Jacobson KA, Hutchison AJ, Williams M, Stiles GL. Proc Natl Acad Sci U S A; 1989 Sep 22; 86(17):6572-6. PubMed ID: 2771944 [Abstract] [Full Text] [Related]
39. N6-Cycloalkyl- and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice. Franchetti P, Cappellacci L, Vita P, Petrelli R, Lavecchia A, Kachler S, Klotz KN, Marabese I, Luongo L, Maione S, Grifantini M. J Med Chem; 2009 Apr 23; 52(8):2393-406. PubMed ID: 19317449 [Abstract] [Full Text] [Related]
40. N6-[2-(3,5-dimethoxyphenyl)-2-(2-methylphenyl)ethyl]adenosine and its uronamide derivatives. Novel adenosine agonists with both high affinity and high selectivity for the adenosine A2 receptor. Bridges AJ, Bruns RF, Ortwine DF, Priebe SR, Szotek DL, Trivedi BK. J Med Chem; 1988 Jul 23; 31(7):1282-5. PubMed ID: 3385722 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]