2′-Deoxyguanosine monohydrate
SIGMA/D7145 - 99-100%
Synonym: 2′-Deoxyguanosine hydrate; 9-(2-Deoxy-β-D-ribofuranosyl)guanine; Guanine-2′-deoxyriboside
CAS Number: 312693-72-4
Empirical Formula (Hill Notation): C10H13N5O4 · H2O
Molecular Weight: 285.26
MDL Number: MFCD00150760
Linear Formula: C10H13N5O4 · H2O
Product Type: Chemical
| assay | 99-100% |
| biological source | synthetic (organic) |
| form | powder |
| InChI | 1S/C10H13N5O4.H2O/c11-10- |
| InChI key | LZSCQUCOIRGCEJ-FPKZOZHISA |
| Quality Level | 200 ![]() |
| SMILES string | O.NC1=Nc2c(ncn2[C@H]3C[C@ |
| solubility | 1 M NH4OH: 50 mg/mL, clear, colorless |
| Application: | 2′-Deoxyguanosine monohydrate has been used as a nucleoside supplement: • to study its effect on mitochondrial DNA copy number in deoxyguanosine kinase (dguok) mutant zebrafish, • in tissue culture medium for deoxyribonucleotide triphosphate (dNTP) synthesis, • in RPMI (Roswell Park Memorial Institute)-1640 medium to eliminate the endogenous thymocytes |
| Biochem/physiol Actions: | Deoxyguanosine (dG) is a purine nucleoside that upon sequential phosphorylation (kinases) forms deoxyguanosine triphosphate (dGTP) which is used by DNA polymerases and reverse transcriptases to synthesize DNA(s). Deoxyguanosine is the most electron-rich of the four canonical bases and includes many nucleophilic sites which are susceptible to oxidative damage. This makes deoxyguanosine and its oxidized derivatives useful reagents to study mechanisms of oxidative damage to nucleosides and nucleotides. |
| Packaging: | 1, 5 g in poly bottle |
| Packaging: | 25, 100 mg in poly bottle |
| Hazard Codes | Xn |
| Risk Statements | 22 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 99-100% |
| UNSPSC | 41106305 |

