
N6-(2-Phenylethyl)adenosine
CAS No. 20125-39-7
N6-(2-Phenylethyl)adenosine( N6-Phenethyladenosine | N6-Phenylethyladenosine )
Catalog No. M26319 CAS No. 20125-39-7
N6-(2-Phenylethyl)adenosine is an adenosine derivative and an agonist of adenosine receptors with Ki values of 11.8 nM and 30.1 nM for rat and human A1.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 27 | Get Quote |
![]() ![]() |
10MG | 42 | Get Quote |
![]() ![]() |
25MG | 86 | Get Quote |
![]() ![]() |
50MG | 168 | Get Quote |
![]() ![]() |
100MG | 294 | Get Quote |
![]() ![]() |
200MG | 528 | Get Quote |
![]() ![]() |
500MG | 830 | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameN6-(2-Phenylethyl)adenosine
-
NoteResearch use only, not for human use.
-
Brief DescriptionN6-(2-Phenylethyl)adenosine is an adenosine derivative and an agonist of adenosine receptors with Ki values of 11.8 nM and 30.1 nM for rat and human A1.
-
DescriptionN6-(2-Phenylethyl)adenosine is an adenosine derivative and an agonist of adenosine receptors with Ki values of 11.8 nM and 30.1 nM for rat and human A1.(In Vitro):The Ki value of human A3 is 0.63 nM. In CHO cells, N6-(2-Phenylethyl)adenosine inhibits A2 with IC50s of 560 nM and 2250 nM for rat and human.
-
In VitroN6-(2-Phenylethyl)adenosine (N6-Phenethyladenosine) inhibits rA2AR (IC50=560 nM), hA2AR (IC50=2250 nM) in CHO cells.
-
In Vivo——
-
SynonymsN6-Phenethyladenosine | N6-Phenylethyladenosine
-
PathwayApoptosis
-
TargetAdenosine Receptor
-
Recptorxanthine oxidase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number20125-39-7
-
Formula Weight371.39
-
Molecular FormulaC18H21N5O4
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (269.26 mM)
-
SMILESN(CCC1=CC=CC=C1)C2=C3C(N(C=N3)[C@@]4(O[C@H](CO)[C@@H](O)[C@H]4O)[H])=NC=N2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Nooreen Z, et al. Characterization and evaluation of bioactive polyphenolic constituents from Zanthoxylum armatum DC., a traditionally used plant. Biomed Pharmacother. 2017 May;89:366-375.
molnova catalog



related products
-
8-Cyclopentyl-1,3-di...
8-Cyclopentyl-1,3-dimethylxanthine?is a potent antagonist of adenosine A1 receptor.
-
CI-947
An orally active adenosine receptor agonist that can induce acute cardiovascular toxicity and coronary vascular injury in vivo.
-
PSB 1115
PSB 1115 is an A2B receptor antagonist and can counteract the inhibitory effect of NECA.