SMB01082

Licochalcone C

≥90% (LC/MS-ELSD)

• Synonym(s): (E)-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-1-(4-hydroxyphenyl)prop-2-en-1-one, 4,4′-Dihydroxy-2-methoxy-3-prenylchalcone
• Empirical Formula (Hill Notation): C₂₁H₂₂O₄
• CAS Number: 144506-14-9
• Molecular Weight: 338.40
• MDL number: MFCD20527293
• UNSPSC Code: 12352205
• NACRES: NA.25

Properties

• biological source: plant
• Assay: ≥90% (LC/MS-ELSD)
• form: solid
• mol wt: 338.4
• application(s): metabolomics; vitamins, nutraceuticals, and natural products
• storage temp.: −20°C
• SMILES string: O(C)c1c(c(ccc1\C=C\C(=O)c2ccc(cc2)O)O)CC=C(C)C
• InChI: 1S/C21H22O4/c1-14(2)4-11-18-20(24)13-8-16(21(18)25-3)7-12-19(23)15-5-9-17(22)10-6-15/h4-10,12-13,22,24H,11H2,1-3H3/b12-7+
• InChI key: WBDNTJSRHDSPSR-KPKJPENVSA-N

Description

General description

Licochalcone C is a phenolic flavonoid belonging to the group of Chalcones and dihydrochalcones, commonly found in plants such as Glycyrrhiza inflata and Glycyrrhiza glabra. Existing research suggests that this plant-derived metabolite exhibits various biological activities, including cardioprotective, antibacterial, antioxidant, anti-inflammatory, and anti-apoptotic properties.

Application

It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Biochem/physiol Actions

According to the existing research, Licochalcone C may have an effect on processes related to inflammation and cell death regulation by inhibiting the expression of TNF-α, Caspase and Bcl-2/Bax

Features and Benefits

• High quality compound suitable for multiple research applications
• Compatible with HPLC and mass spectrometry techniques

Other Notes

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Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable