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2',3'-DI-O-ACETYL-5'-R-FLUORO-5'-[(4-METHOXYPHENYL)-SULFINYL-(R/S)S]-ADENOSINE

Compound with spectra: 2 NMR

2',3'-DI-O-ACETYL-5'-R-FLUORO-5'-[(4-METHOXYPHENYL)-SULFINYL-(R/S)S]-ADENOSINE
SpectraBase Compound ID 7A88Q5fNukH
InChI InChI=1S/2C21H22FN5O7S/c2*1-10(28)32-15-16(18(22)35(30)13-6-4-12(31-3)5-7-13)34-21(17(15)33-11(2)29)27-9-26-14-19(23)24-8-25-20(14)27/h2*4-9,15-18,21H,1-3H3,(H2,23,24,25)/t15-,16+,17-,18+,21-,35?;15-,16+,17-,18-,21-,35?/m00/s1
InChIKey BMQXMODIETXHEW-WTIZQBPRSA-N
Mol Weight 1014.99 g/mol
Molecular Formula C42H44F2N10O14S2
Exact Mass 1014.244795 g/mol
Enantiomer InChIKey BMQXMODIETXHEW-MXKJLCLASA-N

View Spectrum of 2',3'-DI-O-ACETYL-5'-R-FLUORO-5'-[(4-METHOXYPHENYL)-SULFINYL-(R/S)S]-ADENOSINE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

View Spectrum of 2',3'-DI-O-ACETYL-5'-R-FLUORO-5'-[(4-METHOXYPHENYL)-SULFINYL-(R/S)S]-ADENOSINE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • 2',3'-DI-O-ACETYL-5'-S-FLUORO-5'-[(4-METHOXYPHENYL)-SULFINYL-(R/S)S]-ADENOSINE
(5'S,S(S))-2',3'-Di-O-Acetyl-5'-chloro-5'-deoxy-5'-[(4-methoxyphenyl)sulfinyl]adensine
9H-Purine, 6-(5-methyl-2-furanyl)-9-(2,3,5-tri-O-acetyl-.beta.-D-ribofuranosyl)-
BENZYL-(S)-3-[9-(2,3,5-TRI-O-ACETYL-BETA-D-RIBOFURANOSYL)-PURIN-6-YL]-2-[(BENZYLOXYCARBONYL)-AMINO]-PROPANOATE
2',3',5'-TRI-O-BENZOYLADENOSINE-6-N-[O,O-BIS-(2-CYANOETHYL)-PHOSPHORAMIDATE]
(2R,3R,4S,5R,6R)-2-(6-((E)-4-acetoxy-3-methylbut-2-enylamino)-9H-purin-9-yl)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
6-Chloro-2-(N'-methyl-2'-pyrrolyl)-9.beta.-(2',3',5'-tri-O-acetyl)-D,ribo-furanosylpurine
NECA 3AC @
(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(6-(furan-3-ylmethylamino)-9H-purin-9-yl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
ZFJSNPUZOPWRCM-TUDPUUEGSA-N
(2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-(6-(3-methylbut-2-enylamino)-9H-purin-9-yl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
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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