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3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors
3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors
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3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors
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3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors
3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors

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3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors
3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors
Journal Article

3HXanthine Amine Congener of 1,3-dipropyl-8-phenylxanthine: An Antagonist Radioligand for Adenosine Receptors

1986
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Overview
An amine-functionalized derivative of 1,3-dipropyl-8-phenylxanthine has been prepared in tritiated form as a xanthine amine congener [3H]XAC) for use as an antagonist radioligand for adenosine receptors. [3H]XAC has higher receptor affinity, higher specific activity, lower nonspecific membrane binding, and more favorable hydrophilicity than 1,3-diethyl-8-[3H]phenylxanthine, the xanthine commonly used for adenosine receptor binding. In rat cerebral cortical membranes, [3H]XAC exhibits saturable, specific binding with a Kd of 1.23 nM and a Bmax of 580 fmol/mg of protein at 37 degrees C. N6-(R-Phenylisopropyl)adenosine is a more potent inhibitor of [3XAC binding than is 5′-N-ethylcarboxamidoadenosine, indicating that binding is to an A1-adenosine receptor. In the absence of GTP, the inhibition curves for adenosine agonists versus [3H]XAC binding are biphasic, indicating that [3H]XAC is binding to low- and high-affinity agonist states of the A1 receptor. In the presence of GTP, adenosine analogs exhibit monophasic, low-affinity inhibition of binding of [3H]XAC. Inhibition of [3H]XAC binding by theophylline or by various 8-phenylxanthines is monophasic, and the potencies are commensurate with the potencies of these xanthines as adenosine receptor antagonists. The receptor sites in calf brain membranes exhibit a higher affinity (Kd = 0.17 nM) for [3H]XAC, whereas sites in guinea pig exhibit a slightly lower affinity (Kd = 3.0 nM). Densities of [3H]XAC binding sites are similar in brain membranes from all species.