2’-Deoxyadenosine Monohydrate

• CAT Number: R050421
• CAS Number: 16373-93-6
• Molecular Formula: C10H15N5O4
• Molecular Weight: 269.261
• Purity: ≥95%
• Synonyms: 2’-Deoxy-β-D-adenosine Monohydrate; 9-(2-Deoxy-β-D-erythro-pentofuranosyl)adenine; 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-9H-purin-6-amine Hydrate; Adenine Deoxyribonucleoside Hydrate; Adenine Deoxyribose Hydrate; Adenyldeoxyriboside Hydrate; Deoxyad
• Target: Endogenous Metabolite
• Storage: Store at -20°C
• IUPAC Name: (2R,3S,5R)-5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol;hydrate
• InChI: InChI=1S/C10H13N5O3.H2O/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(17)6(2-16)18-7;/h3-7,16-17H,1-2H2,(H2,11,12,13);1H2/t5-,6+,7+;/m0./s1
• InChIKey: WZJWHIMNXWKNTO-VWZUFWLJSA-N
• SMILES: C1C(C(OC1N2C=NC3=C2N=CN=C3N)CO)O.O

2’-Deoxyadenosine Monohydrate (CAS 16373-93-6) 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.

Reference

1.Lakshman, Maheshkumar, and Roland E. Lehr. "Synthesis of polycyclic aromatic hydrocarbon 2′-deoxyadenosine analogs." Tetrahedron letters 31.11 (1990): 1547-1550.
2.Ikejiri, Masahiro, et al. "Synthesis and evaluation of 5′-modified 2′-deoxyadenosine analogues as anti-hepatitis C virus agents." Bioorganic & medicinal chemistry letters 18.16 (2008): 4638-4641.