Free shipping on all orders over $ 500

N6-Cyclohexyladenosine

Cat. No. M29993

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

N6-Cyclohexyladenosine Structure
Synonym:

CHA

Price and Availability

For this product's availability, delivery time and price, please email [email protected] directly or click the "Inquiry Now" button below.


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

Related Adenosine Receptor Products
CV1808

CV1808 (2-Phenylaminoadenosine) is a non-selective A2 adenosine receptor (A2 AR) agonist with Kis of 76 and 1450 nM for A2A and A3 adenosine receptor subtypes, respectively.

FK 453 

FK 453 is a potent and selective adenosine A1 receptor antagonist with an IC50 value of 17.2 nM.

GS-9667

GS-9667 (CVT 3619), a novel N6-5'-substituted adenosine analog, is a selective, partial agonist of the A1 adenosine receptor (A1AdoR).

PD81723 

PD81723 is an adenosine receptor binding enhancer.

PSB-0788 

PSB-0788 is a new selective high-affinity A2B antagonist with IC50 value of 3.64 nM and Ki value of 0.393 nM, respeactively.

  Catalog
Abmole Inhibitor Catalog




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

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2024 AbMole BioScience. All Rights Reserved.