| Weight | 154.165 g/mol |
|---|---|
| Formula | C8H10O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Vanillyl alcohol (498-00-0)
Score:
#1618 in Biochemistry
,
#4627 in Chemistry
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- Crystal structures and inhibitor binding in the octameric flavoenzyme vanillyl-alcohol oxidase: the shape of the active-site cavity controls substrate specificity (Structure, 1997)
- Purification and characterization of vanillyl-alcohol oxidase from Penicillium simplicissimum : a novel aromatic alcohol oxidase containing covalently bound FAD (FEBS Journal, 1992)
- Covalent flavinylation is essential for efficient redox catalysis in vanillyl-alcohol oxidase. (Journal of Biological Chemistry, 1999)
- Detection of intact megaDalton protein assemblies of vanillyl-alcohol oxidase by mass spectrometry. (Protein Science, 2008)
- Formation and Degradation of Furfuryl Alcohol, 5-Methylfurfuryl Alcohol, Vanillyl Alcohol, and Their Ethyl Ethers in Barrel-Aged Wines (Journal of Agricultural and Food Chemistry, 1998)
- Substrate specificity of flavin-dependent vanillyl-alcohol oxidase from Penicillium simplicissimum.Evidence for the production of 4-hydroxycinnamyl alcohols from 4-allylphenols (FEBS Journal, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=C(C=CC(=C1)CO)O
-
InChIKeyZENOXNGFMSCLLL-UHFFFAOYSA-N
- Pubchem - Vanillyl alcohol
- Wikipedia - vanillyl alcohol
Vanillyl alcohol is derived from vanillin. It is used to flavor food.
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Similar Compounds
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326-56-7
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alpha-Ethylpiperonyl alcohol
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Vanillyl alcohol
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