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| Chemical manufacturer since 1992 | ||||
| Classification | Biochemical >> Nucleoside drugs >> Nucleoside intermediate |
|---|---|
| Name | 8-Hydroxyguanosine |
| Synonyms | 2-Amino-9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(Hydroxymethyl)Tetrahydrofuran-2-Yl]-3,7-Dihydropurine-6,8-Dione; 2-Amino-9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(Hydroxymethyl)-2-Tetrahydrofuranyl]-3,7-Dihydropurine-6,8-Dione; 2-Amino-9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-Methylol-Tetrahydrofuran-2-Yl]-3,7-Dihydropurine-6,8-Quinone |
| Molecular Structure | ![]() |
| Molecular Formula | C10H13N5O6 |
| Molecular Weight | 299.24 |
| CAS Registry Number | 3868-31-3 |
| SMILES | [C@H]1(O[C@@H]([C@@H](O)[C@H]1O)CO)N2C3=C(NC2=O)C(=O)N=C(N3)N |
| InChI | 1S/C10H13N5O6/c11-9-13-6-3(7(19)14-9)12-10(20)15(6)8-5(18)4(17)2(1-16)21-8/h2,4-5,8,16-18H,1H2,(H,12,20)(H3,11,13,14,19)/t2-,4-,5-,8-/m1/s1 |
| InChIKey | FPGSEBKFEJEOSA-UMMCILCDSA-N |
| Density | 2.438g/cm3 (Cal.) |
|---|---|
| SDS | Available |
|---|---|
| (1) | Aaron M. Fleming, James G. Muller, Insun Ji and Cynthia J. Burrows. Characterization of 2′-deoxyguanosine oxidation products observed in the Fenton-like system Cu(ii)/H2O2/reductant in nucleoside and oligodeoxynucleotide contexts, Org. Biomol. Chem., 2011, 9, 3338. |
|---|---|
| Market Analysis Reports |
| List of Reports Available for 8-Hydroxyguanosine |