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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

130 related items for PubMed ID: 1895305

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  • 2. N6-substituted 9-methyladenines: a new class of adenosine receptor antagonists.
    Ukena D, Padgett WL, Hong O, Daly JW, Daly DT, Olsson RA.
    FEBS Lett; 1987 May 11; 215(2):203-8. PubMed ID: 3582647
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  • 3. 7-Deaza-2-phenyladenines: structure-activity relationships of potent A1 selective adenosine receptor antagonists.
    Müller CE, Hide I, Daly JW, Rothenhäusler K, Eger K.
    J Med Chem; 1990 Oct 11; 33(10):2822-8. PubMed ID: 2213835
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  • 6. Activity of N6-substituted 2-chloroadenosines at A1 and A2 adenosine receptors.
    Thompson RD, Secunda S, Daly JW, Olsson RA.
    J Med Chem; 1991 Dec 11; 34(12):3388-90. PubMed ID: 1766003
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  • 14. Characterization of the A2 adenosine receptor labeled by [3H]NECA in rat striatal membranes.
    Bruns RF, Lu GH, Pugsley TA.
    Mol Pharmacol; 1986 Apr 11; 29(4):331-46. PubMed ID: 3010074
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  • 15. 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 11; 86(17):6572-6. PubMed ID: 2771944
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  • 18. Influence of the molecular structure of N6-(omega-aminoalkyl)adenosines on adenosine receptor affinity and intrinsic activity.
    Pirovano IM, IJzerman AP, Van Galen PJ, Soudijn W.
    Eur J Pharmacol; 1989 May 11; 172(2):185-93. PubMed ID: 2767141
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  • 19. Trifunctional agents as a design strategy for tailoring ligand properties: irreversible inhibitors of A1 adenosine receptors.
    Boring DL, Ji XD, Zimmet J, Taylor KE, Stiles GL, Jacobson KA.
    Bioconjug Chem; 1991 May 11; 2(2):77-88. PubMed ID: 1868116
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