Comparison of the potency of adenosine as an agonist at human adenosine receptors expressed in Chinese hamster ovary cells

Biochemical Pharmacology

Volumn 61, Issue 4, 2001, Pages 443-448

  Fredholm, Bertil B ^a   Irenius, Eva ^a   Kull, Björn ^a   Schulte, Gunnar ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

Author keywords

Adenosine uptake; Caffeine; Cyclic AMP; Forskolin; Inosine; Xanthines

Indexed keywords

ADENOSINE; ADENOSINE A1 RECEPTOR; ADENOSINE A2 RECEPTOR; ADENOSINE A3 RECEPTOR; CAFFEINE; CYCLIC AMP; FORSKOLIN; INOSINE; NITROBENZYLTHIOINOSINE; PARAXANTHINE; THEOPHYLLINE;

ANALYTIC METHOD; ANIMAL CELL; ARTICLE; CHO CELL; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG EFFICACY; DRUG POTENCY; DRUG RECEPTOR BINDING; DRUG SPECIFICITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RECEPTOR AFFINITY;

ADENOSINE; ANIMALS; CAFFEINE; CHO CELLS; CRICETINAE; CRICETULUS; CYCLIC AMP; DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; INOSINE; RECEPTORS, PURINERGIC P1; THEOBROMINE; THEOPHYLLINE; TRANSFECTION;

EID: 0035865444     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-2952(00)00570-0     Document Type: Article

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