Structure via PubChem · Public domain (PubChem)
تیروسول
Sign in to saveAlso known as 4-Hydroxybenzeneethanol, p-Hydroxyphenethyl alcohol, 4-(2-hydroxyethyl)phenol, 4-Hydroxyphenylethyl alcohol, beta-(4-Hydroxyphenyl)ethanol, 2-(p-Hydroxyphenyl)ethanol, b-(p-Hydroxyphenyl)ethanol, 4-Hydroxyphenethyl alcohol
ترکیب شیمیایی
Chemical data
- Formula
- C8H10O2
- Molecular weight
- 138.16 g/mol
- IUPAC name
- 4-(2-hydroxyethyl)phenol
- SMILES
- C1=CC(=CC=C1CCO)O
- InChIKey
- YCCILVSKPBXVIP-UHFFFAOYSA-N
- XLogP
- 0.4
- Polar surface area
- 40.5 Ų
- H-bond donors
- 2
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
1,558 papers- Tyrosol as a Neuroprotector: Strong Effects of a "Weak" Antioxidant.Current neuropharmacology · 2021
- Inhibition of the NF-κB/HIF-1α signaling pathway in colorectal cancer by tyrosol: a gut microbiota-derived metabolite.Journal for immunotherapy of cancer · 2024
- Hydroxytyrosol, Tyrosol and Derivatives and Their Potential Effects on Human Health.Molecules (Basel, Switzerland) · 2019
- Tyrosol Modifications for Improved Functionality: A Review of Hydrophilic and Lipophilic Pathways and Their Potential Applications.Journal of agricultural and food chemistry · 2025
- Farnesol and Tyrosol: Secondary Metabolites with a Crucial quorum-sensing Role in Candida Biofilm Development.Genes · 2020
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 138.068
Show 6 more facts
- found in taxon
- Vitis vinifera
- chemical formula
- C₈H₁₀O₂
- subject has role
- antiarrhythmic agent
- canonical SMILES
- C1=CC(=CC=C1CCO)O
- melting point
- 91
- Commons category
- Tyrosol
via Wikidata · CC0