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DPCPX is an adenosine A1 receptor antagonist (Ki = 0.3 nM).1 It is selective for the adenosine A1 receptor over the adenosine A2 receptor (Ki = 340 nM). DPCPX (0.03 and 1 µM) increases the force of contractions in isolated guinea pig left auricles and inhibits decreases in contraction forces induced by the adenosine receptor agonists (–)-N6-phenylisopropyladenosine (PIA) or 5'-N-ethylcarboxamidoadenosine (NECA; Item No. 21420) in isolated guinea pig papillary muscles (pA2s = 9.3 and 9, respectively).2 It reverses cardiac arrest induced by adenosine, the adenosine A1 receptor agonist N6-cyclopentyladenosine (CPA; Item No. 21448), or the acetylcholine receptor agonist carbachol (carbamoylcholine; Item No. 14486) in isolated rat atrium.3 DPCPX (2 and 4 mg/kg) decreases immobility time in the forced swim test and tail suspension test in mice.4
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3. Cardiac arrest induced by muscarinic or adenosine receptors agonists is reversed by DPCPX through double mechanism. Eur. J. Pharmacol. 819, 9-15 (2018).
4. DPCPX, a selective adenosine A1 receptor antagonist, enhances the antidepressant-