A specific adenosine A2 receptor agonist
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5'-(N-Cyclopropyl)carboxamidoadenosine

Item No. 18157

Technical Information
Formal Name
1-(6-amino-9H-purin-9-yl)-N-cyclopropyl-1-deoxy-β-D-ribofuranuronamide
CAS Number
50908-62-8
Synonyms
  • CPCA
Molecular Formula
C13H16N6O4
Formula Weight
Purity
≥95%
Formulation
A crystalline solid
DMF: 25 mg/mlDMSO: 14 mg/mlEthanol: 2 mg/mlPBS (pH 7.2): 10 mg/ml
λmax
259 nm
SMILES
O[C@H]1[C@H](N2C=NC3=C2N=CN=C3N)O[C@H](C(NC4CC4)=O)[C@H]1O
InChi Code
InChI=1S/C13H16N6O4/c14-10-6-11(16-3-15-10)19(4-17-6)13-8(21)7(20)9(23-13)12(22)18-5-1-2-5/h3-5,7-9,13,20-21H,1-2H2,(H,18,22)(H2,14,15,16)/t7-,8+,9-,13+/m0/s1
InChi Key
MYNRELUCFAQMFC-QRIDJOKKSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    5'-(N-Cyclopropyl)carboxamidoadenosine is a specific adenosine A2 receptor agonist with antipyretic and anticonvulsant activity.1,2 It stimulates the production of cyclic AMP in CHO-K1 cells with an EC50 value of 5.3 µM.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Gagalo, I.T., and Matuszek, M.T. The effect of N6-cyclohexyladenosine and 5'-(N-cyclopropyl)-carboxamidoadenosine on pyrogen fever in rabbits. Ann. N. Y. Acad. Sci. 813(1), 353-359 (1997).

    2. Huber, A., Güttinger, M., Möhler, H., et alSeizure suppression by adenosine A2A receptor activation in a rat model of audiogenic brainstem epilepsy. Neurosci. Lett. 329, 289-292 (2002).

    3. de Zwart, M., Link, R., von Frijtag Drabbe Künzel, J.K., et alA functional screening of adenosine analogues at the adenosine A2B receptor: a search for potent agonists. Nucleosides Nucleotides 17(6), 969-985 (1998).