SMB01082

Licochalcone C

≥90% (LC/MS-ELSD)

• Synonyme(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
• Formule empirique (notation de Hill): C₂₁H₂₂O₄
• Numéro CAS: 144506-14-9
• Poids moléculaire : 338.40
• Numéro MDL: MFCD20527293
• Code UNSPSC : 12352205
• Nomenclature NACRES : NA.25

Propriétés

• Source biologique: plant
• Pureté: ≥90% (LC/MS-ELSD)
• Forme: solid
• Poids mol.: 338.4
• Application(s): metabolomics; vitamins, nutraceuticals, and natural products
• Température de stockage: −20°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+
• Clé InChI: WBDNTJSRHDSPSR-KPKJPENVSA-N

Description

Description générale

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.

Actions biochimiques/physiologiques

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

Caractéristiques et avantages

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

Autres remarques

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Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable