KXLYDMYMNDAXPA-RYVZHVEOSA-N
Compound with spectra: 2 NMR
| SpectraBase Compound ID | Jpbx2YxZaZb |
|---|---|
| InChI | InChI=1S/C11H15N5O3S/c1-20-8-7(18)5(2-17)19-11(8)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17-18H,2H2,1H3,(H2,12,13,14)/t5-,7-,8-,11-/m0/s1 |
| InChIKey | KXLYDMYMNDAXPA-RYVZHVEOSA-N |
| Mol Weight | 297.33 g/mol |
| Molecular Formula | C11H15N5O3S |
| Exact Mass | 297.089561 g/mol |
| Enantiomer InChIKey | KXLYDMYMNDAXPA-IOSLPCCCSA-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'-DEOXY-2'-METHYLTHIOADENOSINE
Adenosine, 2'-O-methyl-
2'-O-methyl-adenosine
5-Deoxy-5-dimethylamino-adenosine
GNYFNLGMSBCRCL-HEWDHTHVSA-N
5'-O-CARBAZOYLADENOSINE
5'-S-PROPIONYL-5'-THIOADENOSINE
VVOGAKOZLAELJN-VHMYRRENSA-N
(2R,3R,4S,5S)-2-(6-aminopurin-9-yl)-5-[(methylthio)methyl]tetrahydrofuran-3,4-diol
5'-S-METHYL-5'-THIOADENOSINE
| Title | Journal or Book | Year |
|---|---|---|
| Nucleic Acid Related Compounds. 91. Biomimetic Reactions Are in Harmony with Loss of 2‘-Substituents as Free Radicals (Not Anions) during Mechanism-Based Inactivation of Ribonucleotide Reductases. Differential Interactions of Azide, Halogen, and Alkylthio Groups with Tributylstannane and Triphenylsilane1 | Journal of the American Chemical Society | 1996 |
| Synthesis and conformational properties of 2′-deoxy-2′-methylthio-pyrimidine and -purine nucleosides: Potential antisense applications | Journal of Heterocyclic Chemistry | 1993 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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