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Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O2
Molecular Weight 138.1638
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Tyrosol

SMILES

OCCC1=CC=C(O)C=C1

InChI

InChIKey=YCCILVSKPBXVIP-UHFFFAOYSA-N
InChI=1S/C8H10O2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10H,5-6H2

HIDE SMILES / InChI

Molecular Formula C8H10O2
Molecular Weight 138.1638
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Isolation and characterization of a novel Bacillus sp., strain YAS1, capable of transforming tyrosol under hypersaline conditions.
2005-11-01
Effects of polyphenols on human Th1 and Th2 cytokine production.
2005-10
Electrophoretic identification and quantitation of compounds in the polyphenolic fraction of extra-virgin olive oil.
2005-09
Synthesis of hydroxytyrosol, 2-hydroxyphenylacetic acid, and 3-hydroxyphenylacetic acid by differential conversion of tyrosol isomers using Serratia marcescens strain.
2005-08-10
Development of a sensitive and specific solid phase extraction--gas chromatography-tandem mass spectrometry method for the determination of elenolic acid, hydroxytyrosol, and tyrosol in rat urine.
2005-08-10
Metabolites from endophytes of the medicinal plant Erythrina crista-galli.
2005-07-27
DNA protecting and genotoxic effects of olive oil related components in cells exposed to hydrogen peroxide.
2005-07
Fluorescence spectroscopy for monitoring deterioration of extra virgin olive oil during heating.
2005-07
Kinetic study of the physicochemical and microbiological changes in "seasoned" olives during the shelf-life period.
2005-06-29
Effect of the conservation procedure on the contents of phenolic compounds and organic acids in chanterelle (Cantharellus cibarius) mushroom.
2005-06-15
Separation and identification of phenolic compounds in olive oil by coupling high-performance liquid chromatography with postcolumn solid-phase extraction to nuclear magnetic resonance spectroscopy (LC-SPE-NMR).
2005-06-15
[Studies on chemical constituents from the corm of Cremastra appendiculata].
2005-04
Differential anti-inflammatory effects of phenolic compounds from extra virgin olive oil identified in human whole blood cultures.
2005-03
Secoiridoids, tocopherols, and antioxidant activity of monovarietal extra virgin olive oils extracted from destoned fruits.
2005-02-23
New phenolic glycosides from the seeds of Cucurbita moschata.
2005-02
Activity of olive oil phenols on lymphomonocyte cytosolic calcium.
2005-02
Antioxidant and anti-atherogenic activities of olive oil phenolics.
2005-01
Phenolic compounds in olive oils intended for refining: formation of 4-ethylphenol during olive paste storage.
2004-12-29
Olive oil and modulation of cell signaling in disease prevention.
2004-12
Antifungal and sprout regulatory bioactivities of phenylacetic acid, indole-3-acetic acid, and tyrosol isolated from the potato dry rot suppressive bacterium Enterobacter cloacae S11:T:07.
2004-12
Qualitative and semiquantitative analysis of phenolic compounds in extra virgin olive oils as a function of the ripening degree of olive fruits by different analytical techniques.
2004-11-17
Analysis of minor components in olive oil.
2004-10-29
Identification of compounds in wine by HPLC-tandem mass spectrometry.
2004-10-28
Acid-induced structural modifications of unsaturated Fatty acids and phenolic olive oil constituents by nitrite ions: a chemical assessment.
2004-10
[One new phenylethanoid glycoside from Corallodiscus flabellata].
2004-09
Olives and olive oil in cancer prevention.
2004-08
Removal of monomeric phenols in dry mill olive residue by saprobic fungi.
2004-07-14
Low-molecular-weight components of olive oil mill waste-waters.
2004-06-19
[Protection of Saccharomyces cerevisiae against oxidative and radiation-caused damage by alkyl hydroxybenzenes].
2004-06-17
Effects of differing phenolic content in dietary olive oils on lipids and LDL oxidation--a randomized controlled trial.
2004-06
Bioavailability and antioxidant effects of olive oil phenols in humans: a review.
2004-06
Phenolic antioxidants and the protection of low density lipoprotein from peroxynitrite-mediated oxidations at physiologic CO2.
2004-05-19
Silvestrol and episilvestrol, potential anticancer rocaglate derivatives from Aglaia silvestris.
2004-05-14
Use of apple seed meal as a new source of beta-glucosidase for enzymatic glucosylation of 4-substituted benzyl alcohols and tyrosol in monophasic aqueous-dioxane medium.
2004-05-03
A mild photochemical approach to the degradation of phenols from olive oil mill wastewater.
2004-05
Comparison of the radical scavenging potential of polar and lipidic fractions of olive oil and other vegetable oils under normal conditions and after thermal treatment.
2004-04-21
Polyphenol changes during fermentation of naturally black olives.
2004-04-07
Depsides from the petals of Papaver rhoeas.
2004-04
Attenuation of lipid peroxidation by antioxidants in rat-1 fibroblasts: comparison of the lipid peroxidation reporter molecules cis-parinaric acid and C11-BODIPY(581/591) in a biological setting.
2004-03-22
Decrease of heat shock protein levels and cell populations by wine phenolic extracts.
2004-02-25
LC-MS investigation of oxidation products of phenolic antioxidants.
2004-02-25
Effect of cultivar and processing method on the contents of polyphenols in table olives.
2004-02-11
Phenolic components of Olea europaea--isolation of tyrosol derivatives.
2004-02
Biogenic amine formation and "zapatera" spoilage of fermented green olives: effect of storage temperature and debittering process.
2004-01
Bioavailability of phenolic compounds from olive oil and oxidative/antioxidant status at postprandial state in healthy humans.
2004
Interaction of olive oil phenol antioxidant components with low-density lipoprotein.
2004
[Experimental analysis of therapeutic properties of Rhodiola rosea L. and its possible application in medicine].
2004
Tyrosinase scavenges tyrosyl radical.
2003-12-19
Bhimamycin A to approximately E and bhimanone: isolation, structure elucidation and biological activity of novel quinone antibiotics from a terrestrial Streptomycete.
2003-11
Bioavailability of tyrosol, an antioxidant phenolic compound present in wine and olive oil, in humans.
2003
Patents
Substance Class Chemical
Created
by admin
on Wed Apr 02 18:40:35 GMT 2025
Edited
by admin
on Wed Apr 02 18:40:35 GMT 2025
Record UNII
1AK4MU3SNX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Tyrosol
MI  
INCI  
Official Name English
4-Hydroxyphenethyl alcohol
Preferred Name English
4-Hydroxyphenethyl alcohol [ISO]
Common Name English
TYROSOL (CONSTITUENT OF RHODIOLA ROSEA) [DSC]
Common Name English
TYROSOL [MI]
Common Name English
NSC-59876
Code English
2-(4-HYDROXYPHENYL)ETHANOL
Systematic Name English
METOPROLOL TARTRATE IMPURITY G [EP IMPURITY]
Common Name English
4-HYDROXYBENZENEETHANOL
Systematic Name English
4-(2-HYDROXYETHYL)PHENOL
Systematic Name English
HYDROXYPHENETHYL ALCOHOL, P-
Common Name English
METOPROLOL SUCCINATE IMPURITY G [EP IMPURITY]
Common Name English
Classification Tree Code System Code
DSLD 3467 (Number of products:10)
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
207-930-8
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID8060111
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
FDA UNII
1AK4MU3SNX
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
WIKIPEDIA
TYROSOL
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
MESH
C011867
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
NSC
59876
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
SMS_ID
300000034946
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
CAS
501-94-0
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
CHEBI
1879
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
MERCK INDEX
m11292
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY Merck Index
PUBCHEM
10393
Created by admin on Wed Apr 02 18:40:35 GMT 2025 , Edited by admin on Wed Apr 02 18:40:35 GMT 2025
PRIMARY
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Related Record Type Details
PARENT -> IMPURITY
PARENT -> IMPURITY