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N6-Cyclohexyladenosine

Cat. No. M29993

All AbMole products are for research use only, cannot be used for human consumption.

N6-Cyclohexyladenosine Structure
Synonym:

CHA

Size Price Availability Quantity
5mg USD 38 In stock
10mg USD 60 In stock
25mg USD 120 In stock
50mg USD 210 In stock
100mg USD 310 In stock
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Quality Control & Documentation
Biological Activity

N6-Cyclohexyladenosine is a selective A1 receptor agonist (EC50 = 8.2 nM). IC50 value: 8.2 nM (EC50) Target: A1 receptor in vivo: N6-Cyclohexyladenosine exerts anticonvulsant effects and protects against neuronal death. CHA was also found to inhibit the pressor effects of lumbar sympathetic nerve stimulation in rats.

Chemical Information
Molecular Weight 349.38
Formula C16H23N5O4
CAS Number 36396-99-3
Form Solid
Solubility (25°C) DMSO ≥ 100 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Mostafa A Rabie, et al. Chem Biol Interact. Adenosine A1 receptor agonist, N6-cyclohexyladenosine, attenuates Huntington's disease via stimulation of TrKB/PI3K/Akt/CREB/BDNF pathway in 3-nitropropionic acid rat model

[2] A A Assi. J Pharm Pharm Sci. N6-cyclohexyladenosine and 3-(2-carboxypiperazine-4-yl)-1-propenyl-1-phosphonic acid enhance the effect of antiepileptic drugs against induced seizures in mice

[3] M Matuszek, et al. Gen Pharmacol. The effect of N6-cyclohexyladenosine and 5'-N-ethylcarboxamidoadenosine on body temperature in normothermic rabbits

[4] A P Simões, et al. J Neurochem. N6-cyclohexyladenosine inhibits veratridine-stimulated 22Na uptake by rat brain synaptosomes

[5] R L Weir, et al. Epilepsia. Inhibition of N6-[3H]cyclohexyladenosine binding by carbamazepine

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Keywords: N6-Cyclohexyladenosine, CHA supplier, Adenosine Receptor, inhibitors, activators

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