973-67-1
Chemical Structure
5,6,7-Trimethoxyflavone
Synonym(s): Baicalein trimethyl ether
- CAS No.: 973-67-1
- Formula:C18H16O5
- Molecular Weight:312.32
IUPAC Name: 5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one
InChIKey: HJNJAUYFFFOFBW-UHFFFAOYSA-N
SMILES: O=C1C=C(C2=CC=CC=C2)OC3=CC(OC)=C(OC)C(OC)=C13
Biological Activity: 5,6,7-Trimethoxyflavone is a flavonoid compound that can be isolated from plants Callicarpa japonica. 5,6,7-Trimethoxyflavone exhibits antiviral and anti-inflammatory activities through inhibition of NF-κB/AP-1/STAT signaling pathway[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
5,6,7-Trimethoxyflavone | 98.02% | 5,6,7-Trimethoxyflavone is a flavonoid compound that can be isolated from plants Callicarpa japonica. 5,6,7-Trimethoxyflavone exhibits antiviral and anti-inflammatory activities through inhibition of NF-κB/AP-1/STAT signaling pathway. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Hayashi K, et al., Antiviral activity of 5,6,7-trimethoxyflavone and its potentiation of the antiherpes activity of acyclovir. J Antimicrob Chemother. 1997 Jun;39(6):821-4. [Content Brief]
- [2]. Rim HK, et al., 5,6,7-trimethoxyflavone suppresses pro-inflammatory mediators in lipopolysaccharide-induced RAW 264.7 macrophages and protects mice from lethal endotoxin shock. Food Chem Toxicol. 2013 Dec;62:847-55. [Content Brief]
Keywords