9-[(2-HYDROXY-1-(HYDROXYMETHYL)-ETHOXY]-METHYL]-2-AMINOPURINE
Compound with spectra: 1 NMR
![9-[(2-HYDROXY-1-(HYDROXYMETHYL)-ETHOXY]-METHYL]-2-AMINOPURINE](/api/compound/FQu3PJhBuak.png?ph=true&h=300&w=458 "9-[(2-HYDROXY-1-(HYDROXYMETHYL)-ETHOXY]-METHYL]-2-AMINOPURINE")
| SpectraBase Compound ID | FQu3PJhBuak |
|---|---|
| InChI | InChI=1S/C9H13N5O3/c10-9-11-1-7-8(13-9)14(4-12-7)5-17-6(2-15)3-16/h1,4,6,15-16H,2-3,5H2,(H2,10,11,13) |
| InChIKey | WVDCJUSYASXINB-UHFFFAOYSA-N |
| Mol Weight | 239.23 g/mol |
| Molecular Formula | C9H13N5O3 |
| Exact Mass | 239.101839 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
Famciclovir-M (bis-deacetyl-)
2-(6-CHLORO-PURIN-9-YLMETHOXY)-ETHANOL
2-(6-CHLORO-PURIN-9-YLMETHOXY)-ETHYL-ACETATE
9-[(2-HYDROXYETHOXY)-METHYL]-ADENINE
9-(3-Methylbut-2-enyl)adenine
1-Pentanol, 5-(6-chloro-9H-9-purinyl)
9-(5-aminopentyl)-adenine-dihydrochloride
6-(6-Amino-9H-purin-9-yl)-1-hexanol
9-NONYLADENINE
9-(But-1-en-1-yl)-6-chloro-9H-purine
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of a purine acyclonucleoside series having pronounced antiviral activity. The glyceropurines | Canadian Journal of Chemistry | 1984 |