2-AMINO-7-(2,3-DIDEOXY-3-FLUORO-BETA-D-ERYTHRO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDIN-4(3H)-ONE
Compound with spectra: 2 NMR
![2-AMINO-7-(2,3-DIDEOXY-3-FLUORO-BETA-D-ERYTHRO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDIN-4(3H)-ONE](/api/compound/7fQzq4bGjTG.png?ph=true&h=300&w=458 "2-AMINO-7-(2,3-DIDEOXY-3-FLUORO-BETA-D-ERYTHRO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDIN-4(3H)-ONE")
| SpectraBase Compound ID | 7fQzq4bGjTG |
|---|---|
| InChI | InChI=1S/C11H13FN4O3/c12-6-3-8(19-7(6)4-17)16-2-1-5-9(16)14-11(13)15-10(5)18/h1-2,6-8,17H,3-4H2,(H3,13,14,15,18)/t6-,7+,8+/m0/s1 |
| InChIKey | UQVJVMWNNIXSCR-XLPZGREQSA-N |
| Mol Weight | 268.25 g/mol |
| Molecular Formula | C11H13FN4O3 |
| Exact Mass | 268.097168 g/mol |
| Enantiomer InChIKey | UQVJVMWNNIXSCR-CSMHCCOUSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
2-Amino-7-(2-deoxy-B-D-erythro-pentafuranosyl)-3,7-dihydro-pyrrolo(2,3-D)pyrimidin-4-one
2-AMINO-7-(2-DEOXY-BETA-D-THREO-PENTOFURANOSYL)-7H-PYRROLO-[2,3-D]-PYRIMIDIN-4(3H)-ONE
2-amino-7-[(2R,4S,5R)-4-hydroxy-5-methylol-tetrahydrofuran-2-yl]-1H-pyrrolo[3,2-e]pyrimidin-4-one
6-AMINO-1-(2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSYL)-1H-PYRAZOLO-[3.4-D]-PYRIMIDIN-4(5H)-ONE;8-AZA-7-DEAZA-2'-DEOXY-GUANOSINE
2'-Deoxyguanosine
6-CHLORO-2'-DEOXY-3,7-DIDEAZA-INOSINE
2-AMINO-9-(2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSYL)-6-MERCAPTO-9H-PURINE
1-AMINO-2'-DEOXYINOSINE
5-AMINO-3-(2-DEOXY-BETA-D-ERYTHRO-PENTOFURANOSYL)-3H-1,2,3-TRIAZOLO-[4,5-D]-PYRIMIDINE-7(6H)-ONE
N1-HYDROXY-2'-DEOXYINOSINE
| Title | Journal or Book | Year |
|---|---|---|
| 3′‐Substituted and 2′,3′‐Unsaturated 7‐Deazaguanine 2′,3′‐Dideoxynucleosides: Syntheses and Inhibition of HIV‐1 Reverse Transcriptase | Helvetica Chimica Acta | 1991 |