Xanthine derivatives as antagonists at A1 and A2 adenosine receptors-Reference-Cited by-同舟云学术

Xanthine derivatives as antagonists at A1 and A2 adenosine receptors

Published:1985-09 Issue:3 Volume:330 Page:212-221
ISSN:0028-1298
Container-title:Naunyn-Schmiedeberg's Archives of Pharmacology
language:en
Short-container-title:Naunyn-Schmiedeberg's Arch. Pharmacol.

Author:

Schwabe U.,Ukena D.,Lohse M. J.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00572436.pdf

Reference33 articles.

1. Asano T, Ochiai Y, Hidaka H (1977) Selective inhibition of separated forms of human platelet cyclic nucleotide phosphodiesterase by platelet aggregation inhibitors. Mol Pharmacol 13: 400?406

2. Blume AJ, Foster CJ (1975) Mouse neuroblastoma adenylate cyclase. Adenosine and adenosine analogues as potent effectors of adenylate cyclase activity. J Biol Chem 250: 5003?5008

3. Bruns RF (1981) Adenosine antagonism by purines, pteridines and benzopteridines in human fibroblasts. Biochem Pharmacol 30: 325?333

4. Bruns RF, Daly JW, Snyder SH (1980) Adenosine receptors in brain membranes: Binding of N6-cyclohexyl[3H]adenosine and 1,3-diethyl-8-[3H]phenylxanthine. Proc Natl Acad Sci USA 77: 5547?5551

5. Bruns RF, Daly JW, Snyder SH (1983) Adenosine receptor binding: Structure-activity analysis generates extremely potent xanthine antagonists. Proc Natl Acad Sci USA 80: 2077?2080

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