N6-CYCLOHEXYLADENOSINE
N6-CYCLOHEXYLADENOSINE Basic information
- Product Name:
- N6-CYCLOHEXYLADENOSINE
- Synonyms:
-
- CHA
- N6-CYCLOHEXYLADENOSINE
- N6-CYCLOHEXYLADENOSINE (CHA) SELECTIVE A 1 ADENOSIN
- N(sup 6)-cyclohexyladenosine
- Cyclohexyladenosine
- N-Cyclohexyladenosine
- Adenosine, N-cyclohexyl-
- N6-Cyclohexyladenosine,CHA
- CAS:
- 36396-99-3
- MF:
- C16H23N5O4
- MW:
- 349.38
- Mol File:
- 36396-99-3.mol
N6-CYCLOHEXYLADENOSINE Chemical Properties
- Melting point:
- 182 - 184°C
- Boiling point:
- 675.2±65.0 °C(Predicted)
- Density
- 1.71±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 13.12±0.70(Predicted)
- color
- White to Off-White
- Stability:
- Hygroscopic
MSDS
- Language:English Provider:SigmaAldrich
N6-CYCLOHEXYLADENOSINE Usage And Synthesis
Description
N6-Cyclohexyladenosine is an adenosine receptor agonist. It selectively binds to adenosine A1 receptors in rat cortical membranes (IC50 = 2.3 nM) over A2 receptors in rat striatal membranes (IC50 = 870 nM). N6-Cyclohexyladenosine decreases heart rate and increases coronary flow in a perfused working rat heart model ex vivo (EC25s = 5 and 860 nM, respectively). In vivo, it decreases heart rate and blood pressure in normotensive rats (EC25s = 2.4 and 4.2 μg/kg, respectively). N6-Cyclohexyladenosine (100 μM) induces sleep in rats when administered via basal forebrain infusion. N6-Cyclohexyladenosine also decreases locomotor activity in mice (ED50 = 60 μg/kg, i.p.).
Uses
N6-Cyclohexyladenosine is a derivative of Adenosine (A280400), and is used testing adenosine A1 and A2A receptor activation for pharmaceuticals such as antidepressants. N6-Cyclohexyladenosine also is used as a JAK2 inhibitor, blocking STAT3 signalling in human cancer cells.
Biochem/physiol Actions
Selective A1 adenosine receptor agonist.
storage
Store at -20°C
N6-CYCLOHEXYLADENOSINESupplier
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