| Weight | 154.165 g/mol |
|---|---|
| Formula | C8H10O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Hydroxytyrosol (10597-60-1)
Score:
#1540 in Biochemistry
,
#3565 in Biology
,
#4477 in Chemistry
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- Antioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxytyrosol (Food and Chemical Toxicology, 1994)
- On the in-vitro antimicrobial activity of oleuropein and hydroxytyrosol. (Journal of Pharmacy and Pharmacology, 1999)
- Antioxidant Activity of Hydroxytyrosol Acetate Compared with That of Other Olive Oil Polyphenols (Journal of Agricultural and Food Chemistry, 2001)
- Hydroxytyrosol Disposition in Humans (Clinical Chemistry, 2003)
- Bioactive compounds in wine: Resveratrol, hydroxytyrosol and melatonin: A review (Food Chemistry, 2012)
- Pharmacokinetics and Metabolism of Hydroxytyrosol, a Natural Antioxidant from Olive Oil (Drug Metabolism and Disposition, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=C(C=C1CCO)O)O
-
InChIKeyJUUBCHWRXWPFFH-UHFFFAOYSA-N
- Pubchem - Hydroxytyrosol
- Wikipedia - Hydroxytyrosol
Hydroxytyrosol is a phenylethanoid, a type of phenolic phytochemical with antioxidant properties in vitro. In nature, hydroxytyrosol is found in olive leaf and olive oil, in the form of its elenolic acid ester oleuropein and, especially after degradation, in its plain form. Hydroxytyrosol itself in pure form is a colorless, odorless liquid.
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Hydroxytyrosol
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