N6-Ethyladenosine( —— )

Catalog No. M26318 CAS No. 14357-08-5

N6-Ethyladenosine is an adenosine derivative, acts as an agonist of Adenosine receptor(hA1AR and hA3AR with Kis of 4.9 and 4.7 nM , respectively).

Purity : >98% (HPLC)

COA

Datasheet

HNMR

HPLC

MSDS

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Size	Price / USD	Stock	Quantity
1 mL x 10 mM in DMSO	52	In Stock
5MG	30	In Stock
10MG	48	In Stock
25MG	88	In Stock
50MG	145	In Stock
100MG	214	In Stock
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Biological Information

Product Name

N6-Ethyladenosine
Note

Research use only, not for human use.
Brief Description

N6-Ethyladenosine is an adenosine derivative, acts as an agonist of Adenosine receptor(hA1AR and hA3AR with Kis of 4.9 and 4.7 nM , respectively).
Description

N6-Ethyladenosine is an adenosine derivative, acts as an agonist of Adenosine receptor(hA1AR and hA3AR with Kis of 4.9 and 4.7 nM , respectively).(In Vitro):N6-Ethyladenosine exhibits more selectivity at hA1AR and hA3AR over hA2AR with Ki of 8900±770 nM .
In Vitro

N6-Ethyladenosine (Compound 28) exhibits more selectivity at hA1AR and hA3AR over hA2AR (Ki, 8900±770 nM).
In Vivo

——
Synonyms

——
Pathway

Apoptosis
Target

Adenosine Receptor
Recptor

CYP3A4
Research Area

——
Indication

——

Chemical Information

CAS Number

14357-08-5
Formula Weight

295.299
Molecular Formula

C12H17N5O4
Purity

>98% (HPLC)
Solubility

In Vitro:?DMSO : ≥ 83.33 mg/mL (282.20 )
SMILES

CCNc1ncnc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Chemical Name

——

Shipping & Storage Information

Storage

(-20℃)
Shipping

With Ice Pack
Stability

≥ 2 years

Reference

1.Lin CC, et al. Metabolic activation of Pradefovir by CYP3A4 and its potential as an inhibitor or inducer. Antimicrob Agents Chemother. 2006 Sep;50(9):2926-31.

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