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Flavanone

Cat. No. M20411

All AbMole products are for research use only, cannot be used for human consumption.

Flavanone Structure
Synonym:

2,3-Dihydroflavone, 4-Flavanone, 2-Phenyl-4-chromanone, 2-Phenylchroman-4-one

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Quality Control & Documentation
Biological Activity

Flavanones show strong antioxidant and radical scavenging activity, and appear to be associated with a reduced risk of certain chronic diseases, the prevention of some cardiovascular disorders, and certain kinds of cancer. Flavanones also exhibit antiviral, antimicrobial, and anti-inflammatory activities, beneficial effects on capillary fragility, and an ability to inhibit human platelet aggregation, anti-ulcer, and anti-allergenic properties.

Chemical Information
Molecular Weight 224.25
Formula C15H12O2
CAS Number 487-26-3
Solubility (25°C) DMSO 44 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Krishna Somaletha Chandran, et al. Int J Mol Sci. Molecular Characterisation of Flavanone O-methylation in Eucalyptus

[2] Xiao-Qiang Chang, et al. Zhongguo Zhong Yao Za Zhi. [A novel flavanone from Thymus przewalskii]

[3] Mai Thanh Thi Nguyen, et al. Nat Prod Res. A new flavanone derivative from the rhizomes of Boesenbergia pandurata

[4] Helda Tutunchi, et al. Phytother Res. Naringenin, a flavanone with antiviral and anti-inflammatory effects: A promising treatment strategy against COVID-19

[5] Gabriela Maciel Diogo, et al. Molecules. Trypanocidal Activity of Flavanone Derivatives

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Keywords: Flavanone, 2,3-Dihydroflavone, 4-Flavanone, 2-Phenyl-4-chromanone, 2-Phenylchroman-4-one supplier, inhibitors, activators

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