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129 related items for PubMed ID: 2992653

  • 1. PACPX--a substituted xanthine--antagonizes both the A1 and A2 subclasses of the P1-purinoceptor: antagonism of the A2 subclass is competitive but antagonism of the A1 subclass is not.
    Burnstock G, Hoyle CH.
    Br J Pharmacol; 1985 May; 85(1):291-6. PubMed ID: 2992653
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  • 2. Pharmacological analysis of the interaction between purinoceptor agonists and antagonists in the guinea-pig taenia caecum.
    Prentice DJ, Shankley NP, Black JW.
    Br J Pharmacol; 1995 Jun; 115(4):549-56. PubMed ID: 7582471
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  • 3. Apparent affinity of some 8-phenyl-substituted xanthines at adenosine receptors in guinea-pig aorta and atria.
    Collis MG, Jacobson KA, Tomkins DM.
    Br J Pharmacol; 1987 Sep; 92(1):69-75. PubMed ID: 3664093
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  • 4. Activation of P1- and P2Y-purinoceptors by ADP-ribose in the guinea-pig taenia coli, but not of P2X-purinoceptors in the vas deferens.
    Hoyle CH, Edwards GA.
    Br J Pharmacol; 1992 Oct; 107(2):367-74. PubMed ID: 1422586
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  • 10. Functional interaction between purinergic system and opioid withdrawal: in vitro evidence.
    Capasso A, Gallo C.
    Curr Drug Saf; 2009 May; 4(2):97-102. PubMed ID: 19442100
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  • 12. Pre- and postjunctional actions of purine and xanthine compounds in the guinea-pig caecum circular muscle.
    Hoyle CH, Vladimirova IA, Burnstock G.
    Br J Pharmacol; 1988 Oct; 95(2):653-63. PubMed ID: 3228679
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  • 13. Apparent affinity of 1,3-dipropyl-8-cyclopentylxanthine for adenosine A1 and A2 receptors in isolated tissues from guinea-pigs.
    Collis MG, Stoggall SM, Martin FM.
    Br J Pharmacol; 1989 Aug; 97(4):1274-8. PubMed ID: 2790383
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  • 14. Biochemical characterization of the antagonist actions of the xanthines, PACPX (1,3-dipropyl-8(2-amino-4-chloro)phenylxanthine) and 8-PT (8-phenyltheophylline) at adenosine A1 and A2 receptors in rat brain tissue.
    Williams M, Jarvis MF, Sills MA, Ferkany JW, Braunwalder A.
    Biochem Pharmacol; 1987 Nov 15; 36(22):4024-7. PubMed ID: 3689436
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  • 16. Comparison of the potency of 8-phenyltheophylline as an antagonist at A1 and A2 adenosine receptors in atria and aorta from the guinea-pig.
    Collis MG, Palmer DB, Saville VL.
    J Pharm Pharmacol; 1985 Apr 15; 37(4):278-80. PubMed ID: 2860232
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  • 19. Identification and functional characterization of A1 and A2 adenosine receptors in the rat vas deferens: a comparison with A1 receptors in guinea pig left atrium and A2 receptors in guinea pig aorta.
    Martin PL, May JM.
    J Pharmacol Exp Ther; 1994 Jun 15; 269(3):1228-35. PubMed ID: 8014866
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  • 20. 1,3-Dipropyl-8-[2-(5,6-epoxy)norbornyl]xanthine, a potent, specific and selective A1 adenosine receptor antagonist in the guinea pig heart and brain and in DDT1MF-2 cells.
    Belardinelli L, Shryock JC, Zhang Y, Scammells PJ, Olsson R, Dennis D, Milner P, Pfister J, Baker SP.
    J Pharmacol Exp Ther; 1995 Dec 15; 275(3):1167-76. PubMed ID: 8531078
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