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Chemical structure of CAS 958-09-8

Deoxyadenosine

In Stock•Starting at $7 for 1 g•Purity ≥ 98%
CAS No.958-09-8
MDL No.MFCD00005754
MFC10H13N5O3
MW251.24
InChI KeyOLXZPDWKRNYJJZ-RRKCRQDMSA-N

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 g98%$7In Stock
5 g98%$11In Stock
10 g98%$17In Stock
25 g98%$36In Stock
4*25 g98%$140In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

2'-Deoxyadenosine is a purine 2'-deoxyribonucleoside with adenine as the nucleobase. It functions as a metabolite in humans, Saccharomyces cerevisiae, Escherichia coli, and mice. It is classified as a purine 2'-deoxy-D-ribonucleoside and a purine 2'-deoxyribonucleoside.

CAS No.958-09-8
Product NameDeoxyadenosine
IrritantIrritant
Acute ToxicAcute Toxic
Signal Word:Danger
HCode:H315-H319-H335-H301
PCode:P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501-P270-P301+P316-P330

Related Articles

Studies related to this compound and its mechanism of action

Direct detection of 8-oxo-deoxyguanosine using UV resonance Raman spectroscopy.

Photochemistry and photobiology • Vol. 83, Issue 3 • 2007
PMID: 16808627DOI: 10.1562/2006-04-15-RA-876

Inhibition of hepatitis C replicon RNA synthesis by beta-D-2'-deoxy-2'-fluoro-2'-C-methylcytidine: a specific inhibitor of hepatitis C virus replication.

Antiviral chemistry & chemotherapy • Vol. 17, Issue 2 • 2006
PMID: 17042329DOI: 10.1177/095632020601700203

Characterization of glycine N-methyltransferase from rabbit liver.

Biochemistry and cell biology = Biochimie et biologie cellulaire • Vol. 82, Issue 3 • 2004
PMID: 15181470DOI: 10.1139/o04-007

Selectivity of purine alkylation by a quinone methide. Kinetic or thermodynamic control?

The Journal of organic chemistry • Vol. 68, Issue 16 • 2003
PMID: 12895079DOI: 10.1021/jo0346252

Documentation

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