SMB01080
Semilicoisoflavone B
≥85% (LC/MS-ELSD)
Synonym(s):
5,7,8′-Trihydroxy-2′,2′-dimethyl-2′H-(3,6′)bi(1-benzopyranyl)-4-one
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About This Item
Empirical Formula (Hill Notation):
C20H16O6
CAS Number:
Molecular Weight:
352.34
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
biological source
plant
assay
≥85% (LC/MS-ELSD)
form
solid
mol wt
352.34
solubility
water: slightly soluble
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
SMILES string
[o]1c2c([c](c(c1)c3cc4c(c(c3)O)OC(C=C4)(C)C)=O)c(cc(c2)O)O
InChI
1S/C20H16O6/c1-20(2)4-3-10-5-11(6-15(23)19(10)26-20)13-9-25-16-8-12(21)7-14(22)17(16)18(13)24/h3-9,21-23H,1-2H3
InChI key
LWZACZCRAUQSLH-UHFFFAOYSA-N
General description
Semilicoisoflavone B, is an isoflavonoid belongs to the class of 7-hydroxyisoflavones, is a natural product commonly available from Glycyrrhiza Sp., Mitracarpus scaber, and Lentinus tigrinus. This plant metabolite exhibits various biological activities, including anti-inflammatory, antioxidant, anti-tumor, antiviral, and anti-allergic effects.
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
Semilicoisoflavone B:
- Suppresses proinflammatory cytokine production, downregulates TLR4 expression, and diminishes reactive oxygen species generation in vitro.
- Inhibits the growth and division of cancer cells by triggering apoptosis and arresting the cell cycle, offering potential for effective tumor therapy.
- Restricts Caco-2 cell proliferation, suggesting potential for metabolic syndrome therapy.
Features and Benefits
- High quality compound suitable for multiple research applications
- Compatible with HPLC and mass spectrometry techniques
Other Notes
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Storage Class
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
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