5'-S-(4-METHOXYPHENYL)-5'-THIOADENOSINE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | HJIG8USo7Q5 |
|---|---|
| InChI | InChI=1S/C17H19N5O4S/c1-25-9-2-4-10(5-3-9)27-6-11-13(23)14(24)17(26-11)22-8-21-12-15(18)19-7-20-16(12)22/h2-5,7-8,11,13-14,17,23-24H,6H2,1H3,(H2,18,19,20)/t11-,13-,14-,17-/m0/s1 |
| InChIKey | YPBFMIZDPCDUOG-MJFSBKNWSA-N |
| Mol Weight | 389.43 g/mol |
| Molecular Formula | C17H19N5O4S |
| Exact Mass | 389.115775 g/mol |
| Enantiomer InChIKey | YPBFMIZDPCDUOG-LSCFUAHRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
5'-S-(4-CHLOROPHENYL)-5'-THIOADENOSINE
5'-SPHENYL-5'-THIOADENOSINE
5'-S-(3-Amino-3-carboxypropyl)-5'-thio-adenosine
S-Adenosyl-L-homocysteine
5'-S-PROPIONYL-5'-THIOADENOSINE
5'-Adenylic acid disodium salt
Adenosine-5'-monophosphate dianion
9β-D-Arabinofuranosyladenine-5'-monophosphate
VVOGAKOZLAELJN-VHMYRRENSA-N
ADENOSINE-5'-O-MONOTHIOPHOSPHATE
| Title | Journal or Book | Year |
|---|---|---|
| Nucleic Acid Related Compounds. 80. Synthesis of 5'-S-(Alkyl and aryl)-5'-fluoro-5'-thioadenosines with Xenon Difluoride or (Diethylamido)sulfur Trifluoride, Hydrolysis in Aqueous Buffer, and Inhibition of S-Adenosyl-L-homocysteine hydrolase by derived "Adenosine 5'-Aldehyde" Species | The Journal of Organic Chemistry | 1994 |
| Nucleic acid related compounds. 66. Improved syntheses of 5′-chloro-5′-deoxy- and 5′-S-aryl(or alkyl)-5′-thionucleosides | Canadian Journal of Chemistry | 1991 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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