Molecular structure of 2′-Deoxyadenosine monohydrate, CAS Number: 16373-93-6
2′-Deoxyadenosine monohydrate (CAS 16373-93-6)
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Alternate Names:
9-(2-Deoxy-β-D-ribofuranosyl)adenine; Adenine deoxyriboside
Application:
2′-Deoxyadenosine monohydrate is a deoxyribonucleoside
CAS Number:
16373-93-6
Molecular Weight:
269.26
Molecular Formula:
C10H13N5O3•H2O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
2′-Deoxyadenosine monohydrate may affect cAMP levels in some cells. It also may be used as an energy source by some cells under energy stress conditions. 2′-Deoxyadenosine monohydrate can be used in the synthesis of 5′-modified 2′-deoxyadenosine analogues.
2′-Deoxyadenosine monohydrate (CAS 16373-93-6) References
- Synthesis of two 8-[(anthraquinone-2-yl)-linked]-2'-deoxyadenosine 3'-benzyl hydrogen phosphates for studies of photoinduced hole transport in DNA. | Abou-Elkhair, RA. and Netzel, TL. 2005. Nucleosides Nucleotides Nucleic Acids. 24: 85-110. PMID: 15822616
- N6-Arylation of 2'-deoxyadenosine via copper-catalyzed direct coupling with aryl halides. | Ran, C., et al. 2005. J Org Chem. 70: 3724-6. PMID: 15845015
- Increasing surface enhanced Raman spectroscopy effect of RNA and DNA components by changing the pH of silver colloidal suspensions. | Primera-Pedrozo, OM., et al. 2012. Spectrochim Acta A Mol Biomol Spectrosc. 87: 77-85. PMID: 22169024
- Purine 5',8-cyclo-2'-deoxynucleoside lesions: formation by radical stress and repair in human breast epithelial cancer cells. | Krokidis, MG., et al. 2017. Free Radic Res. 51: 470-482. PMID: 28463089
- Proton Transfer Accompanied by the Oxidation of Adenosine. | Choi, J., et al. 2019. Chemistry. 25: 7711-7718. PMID: 30957282
- Increased levels of 5',8-Cyclopurine DNA lesions in inflammatory bowel diseases. | Masi, A., et al. 2020. Redox Biol. 34: 101562. PMID: 32413746
- Proteomics and metabolomics analysis reveal potential mechanism of extended-spectrum β-lactamase production in Escherichia coli. | Ma, H., et al. 2020. RSC Adv. 10: 26862-26873. PMID: 35515772
- Purine nucleosides. XI. The synthesis of 2'-deoxy-9-alpha- and-beta-D-ribofuranosylpurines and the correlation of their anomeric structure with proton magnetic resonance spectra. | Robins, MJ. and Robins, RK. 1965. J Am Chem Soc. 87: 4934-40. PMID: 5844465
- Synchronization of DNA synthesis in Neurospora crassa by 2'-deoxyadenosine and spore selection. | Fletcher, MH. and Trinci, AP. 1980. Arch Microbiol. 128: 113-9. PMID: 6450576
- Chemistry of muconaldehydes of possible relevance to the toxicology of benzene. | Bleasdale, C., et al. 1996. Environ Health Perspect. 104 Suppl 6: 1201-9. PMID: 9118894
- Influence of crystal packing on the solid-state desolvation of purine and pyrimidine hydrates: loss of water of crystallization from thymine monohydrate, cytosine monohydrate, 5-nitrouracil monohydrate, and 2'-deoxyadenosine monohydrate | Perrier, P., & Byrn, S. R. 1982. The Journal of Organic Chemistry. 47(24): 4671-4676.
- Palladium catalysis in the synthesis of 8-position modified adenosine, 2′-deoxyadenosine and guanosine | Tu, C., Keane, C., & Eaton, B. E. 1995. Nucleosides, Nucleotides & Nucleic Acids. 14(8): 1631-1638.
- ibrational modes of nucleoside deoxyadenosine monohydrate investigated under high pressure. | Quimbayo, J. S., Lima, R. A., Vasconcelos, D. L., & Freire, P. T. 2020. Spectroscopy. 110: 103140.
Inhibitor of:
Ada2, ADAT3, Adenosine deaminase, GADD 45α, GTSF1, MTH1, RNase T2, and RNMT.Activator of:
AK3, CNT2, and NXF7.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2′-Deoxyadenosine monohydrate, 250 mg | sc-216290 | 250 mg | $31.00 | |||
2′-Deoxyadenosine monohydrate, 1 g | sc-216290A | 1 g | $46.00 |