Modelling of the pharmacodynamic interaction of an A1 adenosine receptor agonist and antagonist in vivo: N6-cyclopentyladenosine and 8-cyclopentyltheophylline.

समान संसाधन

• Deoxyribose analogues of N6-cyclopentyladenosine (CPA): partial agonists at the adenosine A1 receptor in vivo.
  द्वारा: Mathôt, R. A., और अन्य
  प्रकाशित: (1995)
• Quantification of the In Vivo Potency of the Adenosine A(2) Receptor Antagonist 8-(3-Chlorostyryl)Caffeine
  द्वारा: MATHÔT, RON A. A., और अन्य
  प्रकाशित: (1995)
• Pharmacokinetic-pharmacodynamic modelling of the anti-lipolytic and anti-ketotic effects of the adenosine A(1)-receptor agonist N(6)-(p-sulphophenyl)adenosine in rats
  द्वारा: van Schaick, E A, और अन्य
  प्रकाशित: (1997)
• Selectivity of action of 8-alkylamino analogues of N(6)-cyclopentyladenosine in vivo: haemodynamic versus anti-lipolytic responses in rats
  द्वारा: van Schaick, E A, और अन्य
  प्रकाशित: (1998)
• Pharmacokinetic modelling of the haemodynamic effects of the A2a adenosine receptor agonist CGS 21680C in conscious normotensive rats.
  द्वारा: Mathôt, R A, और अन्य
  प्रकाशित: (1995)