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ARABINOURIDINE
SpectraBase Compound ID A18VaCsiveV
InChI InChI=1S/C9H12N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h1-2,4,6-8,12,14-15H,3H2,(H,10,13,16)
InChIKey DRTQHJPVMGBUCF-UHFFFAOYSA-N
Mol Weight 244.2 g/mol
Molecular Formula C9H12N2O6
Exact Mass 244.069536 g/mol
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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Source of Spectrum PG-1982-1530-0
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Source of Spectrum AV-38-233-2
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Source of Spectrum KO-23-436-0
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Source of Spectrum JZ-1992-1381-0
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Source of Spectrum EP-1642-0-0
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Source of Spectrum EP-4429-0-0
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Source of Spectrum AD-0-3460-0
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Source of Spectrum KO-10-39-2
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Source of Spectrum DB-0-27-10
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Source of Spectrum EP-1752-0-0
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Source of Spectrum EP-1601-0-0
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Source of Spectrum JZ-1992-2012-0
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Source of Spectrum B4-0-0-0
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Solvent DMSO-D6
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Solvent not reported
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Solvent D2O
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Solvent Unknown
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Solvent Unknown
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Solvent H2O
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  • Uridine
  • 1-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-dihydropyrimidine-2,4-dione
  • 1-(3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidine-2,4-dione
Title Journal or Book Year
Structure and conformation of the anticodon nucleoside 5-methoxyuridine in the solid state and in solution Canadian Journal of Chemistry 1983
Constitutional and configurational assignments by13C n.m.r. spectroscopy of Escherichia coli capsular polysaccharides containing ribose and 3-deoxy-D-manno-2-octulosonic acid (KDO) J. Chem. Soc., Chem. Commun. 1982
A 1H and 13C nuclear magnetic resonance study of nucleosides with methylated pyrimidine bases Canadian Journal of Chemistry 1982
Carbon-13 nmr spectra of the tRNA “wobble” nucleosides 5-carboxymethyl-, 5-carbomethoxymethyl-, and 5-carbamoylmethyluridine Journal of Heterocyclic Chemistry 1980

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