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2',3'-DI-O-ACETYL-5'-R-FLUORO-5'-S-METHYL-5'-THIOADENOSINE

Compound with spectra: 1 NMR

2',3'-DI-O-ACETYL-5'-R-FLUORO-5'-S-METHYL-5'-THIOADENOSINE
SpectraBase Compound ID 4dvoW7dszrs
InChI InChI=1S/C15H18FN5O5S/c1-6(22)24-9-10(12(16)27-3)26-15(11(9)25-7(2)23)21-5-20-8-13(17)18-4-19-14(8)21/h4-5,9-12,15H,1-3H3,(H2,17,18,19)/t9-,10+,11-,12+,15-/m0/s1
InChIKey DYJQGDURHLAGOY-NQUGEPOWSA-N
Mol Weight 399.4 g/mol
Molecular Formula C15H18FN5O5S
Exact Mass 399.101268 g/mol
Enantiomer InChIKey DYJQGDURHLAGOY-VNUHZKFNSA-N

View Spectrum of 2',3'-DI-O-ACETYL-5'-R-FLUORO-5'-S-METHYL-5'-THIOADENOSINE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
9-(5-S-Methyl-5-thio-5-fluoro-2,3-di-O-acetyl-.beta.-D-arabinofuranosyl)adenine
2',3'-DI-O-ACETYL-5-DEOXY-5-METHYLTHIO-5-FLUOROADENOSINE
2',3'-DI-O-ACETYL-5'-S-FLUORO-5'-S-METHYL-5'-THIOADENOSINE
2',3'-O-ISOPROPYLIDENE-5-DEOXY-5-METHYLTHIO-5-FLUOROADENOSINE(DIASTEREOMER 1)
(2R,3R,4R,5R)-2-(6-((E)-4-acetoxy-3-methylbut-2-enylamino)-9H-purin-9-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate
(2R,3R,4R,5R)-2-(6-((Z)-4-acetoxy-3-methylbut-2-enylamino)-9H-purin-9-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate
2',3'-Di-O-Acetyl-5'-deoxy-2-fluoro-5'-(methylthio)adenosine
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(dimethylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
[(2R,3R,4R,5R)-3,4-diacetoxy-5-[6-[[4,4,4-trideuterio-3-(trideuteriomethyl)but-2-enyl]amino]purin-9-yl]tetrahydrofuran-2-yl]methyl acetate
(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(3-methylbut-2-enylamino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
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

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