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(-)-ENTERODIOL

Compound with spectra: 2 NMR

(-)-ENTERODIOL
SpectraBase Compound ID ESe8YezcIAD
InChI InChI=1S/C18H22O4/c19-11-15(7-13-3-1-5-17(21)9-13)16(12-20)8-14-4-2-6-18(22)10-14/h1-6,9-10,15-16,19-22H,7-8,11-12H2/t15-,16+
InChIKey DWONJCNDULPHLV-IYBDPMFKSA-N
Mol Weight 302.37 g/mol
Molecular Formula C18H22O4
Exact Mass 302.151809 g/mol

View Spectrum of (-)-ENTERODIOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of (-)-ENTERODIOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
2,3-bis(3-hydroxybenzyl)butane-1,4-diol
1,4-Butanediol, 2,3-bis[(3-hydroxyphenyl-2,4,6-D3)methyl]-, (R*,R*)-
ETHYL(TRANS-3,4-DIBENZYL)ALUMOCYCLOPENTANE
3-Methoxy-4-(3-methoxyphenyl)butan-1-ol
3-[2-(3-methoxyphenyl)ethyl]-2,2-dimethyl-oxirane
1-(3-Methoxyphenyl)-N-methyl-2-pentanamine
1-(3-hydroxyphenyl)-3-oxidanyl-hexan-1-one
cis-2-(4-Methoxymethoxybenzyl)-1-cyclopentanol
4-Methoxy-5-(3-methoxyphenyl)pentan-1-ol
10-(3-methoxyphenyl)-9-oxidanyl-decan-5-one
trans-2-(3,5-dimethylbenzyl)cyclohexan-1-ol
Title Journal or Book Year
Synthesis of (−)-Matairesinol, (−)-Enterolactone, and (−)-Enterodiol from the Natural Lignan Hydroxymatairesinol Organic Letters 2003
Biotransformation of Pinoresinol Diglucoside to Mammalian Lignans by Human Intestinal Microflora, and Isolation of Enterococcus faecalis Strain PDG-1 Responsible for the Transformation of (+)-Pinoresinol to (+)-Lariciresinol Chemical and Pharmaceutical Bulletin 2003

This compound is available in the following databases:

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