Structure via PubChem · Public domain (PubChem)
استوسیرینگون
Sign in to saveAlso known as 4-hydroxy-3,5-dimethoxyacetophenone, 4'-Hydroxy-3',5'-dimethoxyacetophenone, 1-(4-hydroxy-3,5-dimethoxy-phenyl)ethanone, 1-(4-hydroxy-3,5-dimethoxyphenyl)ethanone
Acetosyringone is a phenolic natural product and a chemical compound related to acetophenone and 2,6-dimethoxyphenol. It was first described in relation to lignan/phenylpropanoid-type phytochemicals, with isolation from a variety of plant sources, in particular, in relation to wounding and other physiologic changes.
Chemical data
- Formula
- C10H12O4
- Molecular weight
- 196.2 g/mol
- IUPAC name
- 1-(4-hydroxy-3,5-dimethoxyphenyl)ethanone
- SMILES
- CC(=O)C1=CC(=C(C(=C1)OC)O)OC
- InChIKey
- OJOBTAOGJIWAGB-UHFFFAOYSA-N
- XLogP
- 0.2
- Polar surface area
- 55.8 Ų
- H-bond donors
- 1
- H-bond acceptors
- 4
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
554 papers- Redox active plant phenolic, acetosyringone, for electrogenetic signaling.Scientific reports · 2024
- Metal catalyst-free selective acetosyringone synthesis from rice straw lignin.Environmental science and pollution research international · 2023
- Acetosyringone treatment duration affects large T-DNA molecule transfer to rice callus.BMC biotechnology · 2018
- Inhibition kinetics of acetosyringone on xylanase in hydrolysis of hemicellulose.Bioscience, biotechnology, and biochemistry · 2020
- The Catabolic System of Acetovanillone and Acetosyringone in Sphingobium sp. Strain SYK-6 Useful for Upgrading Aromatic Compounds Obtained through Chemical Lignin Depolymerization.Applied and environmental microbiology · 2022
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 196.074
Show 5 more facts
- found in taxon
- Justicia adhatoda
- chemical formula
- C₁₀H₁₂O₄
- canonical SMILES
- CC(=O)C1=CC(=C(C(=C1)OC)O)OC
- melting point
- 119
- Commons category
- Acetosyringone
via Wikidata · CC0