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
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About This Item
Empirical Formula (Hill Notation):
C21H22O4
CAS Number:
Molecular Weight:
338.40
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
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
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
For additional information on our range of Biochemicals, please complete this form.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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