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
- 1 November 1987
- journal article
- research article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 36 (22) , 4024-4027
- https://doi.org/10.1016/0006-2952(87)90476-x
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Purine Receptors in Mammalian Tissues: Pharmacology and Functional SignificanceAnnual Review of Pharmacology and Toxicology, 1987
- Adenosine A1 receptors in mammalian brain: Species differences in their interactions with agonists and antagonistsDrug Development Research, 1986
- Effects of enprofylline and theophylline may show the role of adenosineLife Sciences, 1986
- Nomenclature of adenosine receptorsTrends in Pharmacological Sciences, 1985
- Functionalized congeners of 1,3-dialkylxanthines: preparation of analogs with high affinity for adenosine receptorsJournal of Medicinal Chemistry, 1985
- Diagnostic and therapeutic use of adenosine in patients with supraventricular tachyarrhythmiasJournal of the American College of Cardiology, 1985
- 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 notBritish Journal of Pharmacology, 1985
- Psychiatric progressJournal of Psychiatric Research, 1984
- The role of adenosine in the regulation of coronary blood flow.Circulation Research, 1980
- Alkylxanthines: Inhibition of adenosine-elicited accumulation of cyclic AMP in brain slices and of brain phosphodiesterase activityLife Sciences, 1979