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Journal Abstract Search
232 related items for PubMed ID: 3018244
1. N6-substituted N-alkyladenosine-5'-uronamides: bifunctional ligands having recognition groups for A1 and A2 adenosine receptors. Olsson RA, Kusachi S, Thompson RD, Ukena D, Padgett W, Daly JW. J Med Chem; 1986 Sep; 29(9):1683-9. PubMed ID: 3018244 [Abstract] [Full Text] [Related]
12. Synthesis and biological activity of a new series of N6-arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido derivatives of adenosine-5'-N-ethyluronamide as A1 and A3 adenosine receptor agonists. Baraldi PG, Cacciari B, Pineda de Las Infantas MJ, Romagnoli R, Spalluto G, Volpini R, Costanzi S, Vittori S, Cristalli G, Melman N, Park KS, Ji XD, Jacobson KA. J Med Chem; 1998 Aug 13; 41(17):3174-85. PubMed ID: 9703463 [Abstract] [Full Text] [Related]
18. Analogs of caffeine: antagonists with selectivity for A2 adenosine receptors. Ukena D, Shamim MT, Padgett W, Daly JW. Life Sci; 1986 Aug 25; 39(8):743-50. PubMed ID: 3016449 [Abstract] [Full Text] [Related]
19. Adenosine derivatives with N6-alkyl, -alkylamine or -alkyladenosine substituents as probes for the A1-receptor. van Galen PJ, Ijzerman AP, Soudijn W. FEBS Lett; 1987 Oct 19; 223(1):197-201. PubMed ID: 2959564 [Abstract] [Full Text] [Related]
20. Dog coronary artery adenosine receptor: structure of the N6-aryl subregion. Kusachi S, Thompson RD, Yamada N, Daly DT, Olsson RA. J Med Chem; 1986 Jun 19; 29(6):989-96. PubMed ID: 3012086 [Abstract] [Full Text] [Related] Page: [Next] [New Search]