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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)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 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
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Product NameN6-(2-Phenylethyl)adenosine
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NoteResearch use only, not for human use.
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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.
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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.
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In VitroN6-(2-Phenylethyl)adenosine (N6-Phenethyladenosine) inhibits rA2AR (IC50=560 nM), hA2AR (IC50=2250 nM) in CHO cells.
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In Vivo——
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SynonymsN6-Phenethyladenosine | N6-Phenylethyladenosine
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PathwayApoptosis
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TargetAdenosine Receptor
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Recptorxanthine oxidase
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Research Area——
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Indication——
Chemical Information
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CAS Number20125-39-7
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Formula Weight371.39
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Molecular FormulaC18H21N5O4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (269.26 mM)
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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
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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.
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