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Antirhinosid

Compound with spectra: 2 NMR

Antirhinosid
SpectraBase Compound ID FfJSgr6EG5v
InChI InChI=1S/C15H22O10/c1-14-9-13(22-3-2-15(9,21)10(20)11(14)25-14)24-12-8(19)7(18)6(17)5(4-16)23-12/h2-3,5-13,16-21H,4H2,1H3/t5-,6-,7+,8-,9?,10+,11-,12+,13-,14+,15-/m0/s1
InChIKey UBAIOTDKPLIEDD-BOHCLOFASA-N
Mol Weight 362.33 g/mol
Molecular Formula C15H22O10
Exact Mass 362.121297 g/mol
Enantiomer InChIKey UBAIOTDKPLIEDD-CQVNSFDJSA-N

View Spectrum of Antirhinosid

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O

View Spectrum of Antirhinosid

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
  • ANTIRRHINOSIDE
ANTIRRINOSIDE
Antirhinosid
Procumbid
6''-O-(TRANS-PARA-COUMAROYL)-PROCUMBIDE
6'-O-PARA-COUMAROYL-PROCUMBINE
BrOMOLINARIOSIDE,(7R,8R)-ISOMER
CAPRARIOSIDE;8-O-BENZOYLHARPAGIDE
LINARIOSIDE,(7R,8R)-ISOMER
BrOMOISOLINARIOOSIDE,(7S,8S)-ISOMER
ISOLINARIOSIDE,(7S,8S)-ISOMER
8-O-PARACOUMAROYLHARPAGIDE
Acetyl-harpagide
6-EPI-8-O-ACETYLHARPAGIDE
Title Journal or Book Year
Halohydrins and Polyols Derived from Antirrhinoside:  Structural Revisions of Muralioside and Epimuralioside Journal of Natural Products 1998
Effect of an 8-hydroxymethyl substituent on the base-catalyzed ring opening of 7,8-epoxyiridoid glucosides The Journal of Organic Chemistry 1983

This compound is available in the following databases:

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Author: Wiley

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Antirhinosid
ANTIRRINOSIDE
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