Licoflaven B Chemical Properties

Boiling point:

593.9±50.0 °C(Predicted)

Density 

1.191±0.06 g/cm3(Predicted)

storage temp. 

-20°C, protect from light

solubility 

Soluble in DMSO

pka

7.57±0.40(Predicted)

form 

Solid

color 

White to yellow

InChI

InChI=1S/C25H26O4/c1-15(2)5-7-17-11-19(9-10-21(17)26)24-14-23(28)20-12-18(8-6-16(3)4)22(27)13-25(20)29-24/h5-6,9-14,26-27H,7-8H2,1-4H3

InChIKey

GLDVIKFETPAZNV-UHFFFAOYSA-N

SMILES

C1(C2=CC=C(O)C(C/C=C(/C)\C)=C2)OC2=CC(O)=C(C/C=C(/C)\C)C=C2C(=O)C=1

Licoflaven B Usage And Synthesis

Uses

Licoflavone B is a flavonoid isolated from Glycyrrhiza inflata, inhibits S. mansoni ATPase (IC50, 23.78 μM) and ADPase (IC50, 31.50 μM) activity. Anti-schistosomiasis activity[1].

Definition

ChEBI: Licoflavone B is a member of flavones.

IC 50

Schistosome

References

[1] Aleixo de Carvalho LS1, et al. Schistosomicidal activity and docking of Schistosoma mansoni ATPDase 1 with licoflavone B isolated from Glycyrrhiza inflata (Fabaceae). DOI:10.1016/j.exppara.2015.09.015

Licoflaven B(91433-17-9)Related Product Information

• 4,4'-DIHYDROXY-2-METHOXYCHALCONE
• Neoisoliquiritin
• SeMilicoisoflavone B
• LIQUIRITIN(SH)
• ISOLIQUIRITIN
• LICOCHALCONE-A
• LICOISOFLAVONE A
• Glycyrrhizic acid ammonium salt
• neoliquiritin
• Isoliquiritigenin
• LICOCHALCONEC
• isoliquiritin apioside
• neoglycyrol
• 18β-Glycyrrhetinic Acid
• GLYCYRRHETIC ACID 3-O-GLUCURONIDE
• METHYL GLYCYRRHIZATE
• LICOFLAVONOL
• Glabridin