1,3,8- and 1,3,7-substituted xanthines: relative potency as adenosine receptor antagonists at the frog neuromuscular junction
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1476-5381.1989.tb11802.x/fullpdf
Reference27 articles.
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2. Adenosine antagonism by purines, pteridines and benzopteridines in human fibroblasts;BRUNS;Biochem. Pharmacol,1981
3. Adenosine receptor binding: structure-activity analysis generates extremely potent xanthine antagonists;BRUNS;Proc. Natl. Acad. Sci. U.S.A.,1983
4. 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;Br. J. Pharmacol,1985
5. Apparent affinity of some 8-phenyl-substituted xanthines at adenosine receptors in guinea-pig aorta and atria;COLLIS;Br. J. Pharmacol,1987
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