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5'-S-METHYL-5'-THIOADENOSINE

Compound with spectra: 2 NMR

5'-S-METHYL-5'-THIOADENOSINE
SpectraBase Compound ID DTUlBnRzXIn
InChI InChI=1S/C11H15N5O3S/c1-20-2-5-7(17)8(18)11(19-5)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 WUUGFSXJNOTRMR-RYVZHVEOSA-N
Mol Weight 297.33 g/mol
Molecular Formula C11H15N5O3S
Exact Mass 297.089561 g/mol
Enantiomer InChIKey WUUGFSXJNOTRMR-IOSLPCCCSA-N

View Spectrum of 5'-S-METHYL-5'-THIOADENOSINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown

View Spectrum of 5'-S-METHYL-5'-THIOADENOSINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
(2R,3S,4S,5S)-2-(6-aminopurin-9-yl)-5-(methylsulfanylmethyl)oxolane-3,4-diol
.beta.-D-Ribofuranose, 1-(6-amino-9H-purin-9-yl)-1-deoxy-5-S-methyl-5-thio-
(2R,3R,4S,5S)-2-(6-aminopurin-9-yl)-5-[(methylthio)methyl]tetrahydrofuran-3,4-diol
5'-S-(FLUOROMETHYL)-5'-THIOADENOSINE
9H-Purin-6-amine, 9-(5-chloro-5-deoxy-.beta.-D-xylofuranosyl)-
(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-(2-chloroethyl)oxolane-3,4-diol
5-Deoxy-5-dimethylamino-adenosine
(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-ethenyl-oxolane-3,4-diol
9-(5,6-Dideoxy-6(E)-iodo-.beta.,D-ribo-hex-5-enfuranosyl)adenine
9-[6-(E/Z)-Chloro-5,6-dideoxy-.beta.,D-ribo-hex-5-enfuranosyl]adenine
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:

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