3,7-Dimethyl-1-propargylxanthine: A potent and selective in vivo antagonist of adenosine analogs
Authors:
- Kathleen A. AblaKAKathleen A. Abla
- Mah T. ShamimMSMah T. Shamim
- John M. CarneyJCJohn M. Carney
- John W. DalyJDJohn W. Daly
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Life Sciences
- Vol. 43 (21) , 1671-1684
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Definition of subclasses of adenosine receptors associated with adenylate cyclase: interaction of adenosine analogs with inhibitory A1 receptors and stimulatory A2 receptorsCanadian Journal of Physiology and Pharmacology, 1987
- Differential antagonism of the behavioral depressant and hypothermic effects of 5′-(N-ethylcarboxamide) adenosine by theobrominePharmacology Biochemistry and Behavior, 1986
- Analogs of 1,3-dipropyl-8-phenylxanthine: enhancement of selectivity at A1-adenosine receptors by aryl substituentsJournal of Medicinal Chemistry, 1986
- Structure-activity relationships for N6-substituted adenosines at a brain A1-adenosine receptor with a comparison to an A2-adenosine receptor regulating coronary blood flowBiochemical Pharmacology, 1986
- Analogs of caffeine and theophylline: effect of structural alterations on affinity at adenosine receptorsJournal of Medicinal Chemistry, 1986
- Adenosine as a NeuromodulatorAnnual Review of Neuroscience, 1985
- Subclasses of adenosine receptors in the central nervous system: Interaction with caffeine and related methylxanthinesCellular and Molecular Neurobiology, 1983
- Xanthine derivatives as adenosine receptor antagonistsEuropean Journal of Pharmacology, 1982
- Adenosine receptors: targets for future drugsJournal of Medicinal Chemistry, 1982
- Adenosine inhibits the accumulation of cyclic AMP in cultured brain cellsNature, 1978