N6-Ethyladenosine
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 574040

CAS#: 14357-08-5

Description: N6-Ethyladenosine is an adenosine A1 and A3 receptor agonist. N6-Ethyladenosine completely inhibits forskolin-induced cAMP accumulation in CHO cells expressing the human recombinant adenosine A3 receptor.


Price and Availability

Size
Price

1mg
USD 235
Size
Price

5mg
USD 525
Size
Price

10mg
USD 900

N6-Ethyladenosine, purity > 98%, is in stock. Current shipping out time is about 2 weeks after order is received. CoA, QC data and MSDS documents are available in one week after order is received.


Chemical Structure

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Theoretical Analysis

MedKoo Cat#: 574040
Name: N6-Ethyladenosine
CAS#: 14357-08-5
Chemical Formula: C12H17N5O4
Exact Mass: 295.1281
Molecular Weight: 295.3
Elemental Analysis: C, 48.81; H, 5.80; N, 23.72; O, 21.67


Synonym: N6-Ethyladenosine, NSC 516603

IUPAC/Chemical Name: N-ethyl-adenosine

InChi Key: SHXVYOLWYFZWKE-WOUKDFQISA-N

InChi Code: InChI=1S/C12H17N5O4/c1-2-13-10-7-11(15-4-14-10)17(5-16-7)12-9(20)8(19)6(3-18)21-12/h4-6,8-9,12,18-20H,2-3H2,1H3,(H,13,14,15)/t6-,8-,9-,12-/m1/s1

SMILES Code: [H][C@]1(O[C@H](CO)[C@@H](O)[C@H]1O)N2C=NC3=C(NCC)N=CN=C32


Technical Data

Appearance:
Solid powder

Purity:
>98% (or refer to the Certificate of Analysis)

Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition:
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility:
Soluble in DMSO

Shelf Life:
>3 years if stored properly

Drug Formulation:
This drug may be formulated in DMSO

Stock Solution Storage:
0 - 4 C for short term (days to weeks), or -20 C for long term (months).

Harmonized System Code:
2934.99.90.01


References

1. Gao, Z.-G., Blaustein, J.B., Gross, A.S., et al. N6-Substituted adenosine derivatives: Selectivity, efficacy, and species differences at A3 adenosine receptors. Biochem. Pharmacol. 65(10), 1675-1684 (2003).