2’-Deoxyguanosine Monohydrate

• CAT Number: R009584
• CAS Number: 312693-72-4
• Molecular Formula: C10H15N5O5
• Molecular Weight: 285.26
• Purity: ≥95%
• Synonyms: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)guanine Monohydrate; Deoxyguanosine Monohydrate; Guanine Deoxyriboside Monohydrate; NSC 22837
• Target: Endogenous Metabolite
• Storage: -20°C
• IUPAC Name: 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one;hydrate
• InChI: InChI=1S/C10H13N5O4.H2O/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6;/h3-6,16-17H,1-2H2,(H3,11,13,14,18);1H2/t4-,5+,6+;/m0./s1
• InChIKey: LZSCQUCOIRGCEJ-FPKZOZHISA-N
• SMILES: C1C(C(OC1N2C=NC3=C2NC(=NC3=O)N)CO)O.O

2’-Deoxyguanosine Monohydrate(CAT: R009584) is a naturally occurring purine nucleoside composed of the base guanine linked to a deoxyribose sugar, with one molecule of water of hydration. It plays a critical role as a building block of DNA, where it pairs with cytosine in the double helix. This compound is widely used in molecular biology, nucleic acid research, and biochemical assays, including studies on DNA replication, repair, and mutagenesis. It is also valuable in the synthesis of oligonucleotides and nucleotide analogs. High-purity 2’-deoxyguanosine monohydrate supports accurate enzymatic reactions and is essential for studies in genomics and pharmaceutical development.