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N6-Cyclopentyladenosine is a selective agonist at adenosine 1 receptors (A1Rs) (Kis = 2.3, 790, and 43 nM for A1R, A2R, and A3R receptors, respectively, in transfected CHO cells).1,2 When microinjected into the rat brainstem, it increases blood pressure and heart rate.3 It is effective for pain in normal and nerve-injured rats and shows anticonvulsant activity in a rat model of generalized seizures.4,5
WARNING This product is not for human or veterinary use.
1. Adenosine receptors and their ligands. Naunyn-Schmiedeberg's Arch. Pharmacol. 362(4), 382-391 (2000).
2. Comparative pharmacology of human adenosine receptor subtypes -
3. Adenosine receptor subtypes in the brainstem mediate distinct cardiovascular response patterns. Brain Res. Bull. 26(1), 59-84 (1991).
4. Differential effects of adenosine A1 receptor on pain-
5. Individual and combined effects of N6-