Liquiritin

From Wikipedia, the free encyclopedia

Liquiritin

Other names Liquiritoside Liquiritigenin-4'-O-glucoside
Identifiers
CAS number	551-15-5
PubChem	503737
	Properties
Molecular formula	C₂₁H₂₂O₉
Molar mass	418.39 g mol⁻¹
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Liquiritin is the 4'-O-glucoside of the flavanone liquiritigenin.

References

Wang, J.; Wang, D.; Yu, J.; Liu, C.; Li, L.; Zhang, Y. (2013). "Isolation of Liquiritigenin-4'-Apiosyl-Glucoside and Liquiritin from the Root of Glycyrrhiza uralensis by High-Performance Centrifugal Partition Chromatography". Journal of Chromatographic Science. doi:10.1093/chromsci/bmt029. ISSN 0021-9665.
Cong, Jing Xiang; Wang, Shao Yan; Gao, Hong (2012). "Separation of Liquiritin by Two-Dimensional Liquid Chromatography". Advanced Materials Research. 455-456: 1232–1238. doi:10.4028/www.scientific.net/AMR.455-456.1232. ISSN 1662-8985.
Cong, Jingxiang; Lin, Bingchang (2007). "Separation of Liquiritin by simulated moving bed chromatography". Journal of Chromatography A 1145 (1-2): 190–194. doi:10.1016/j.chroma.2007.01.088. ISSN 0021-9673.

v t e Flavanones and their glycosides

Flavanones	Alpinetin Butin Eriodictyol Naringenin Pinocembrin

O-methylated flavanones	Hesperetin Homoeriodictyol Isosakuranetin Sakuranetin Sterubin

C-methylated flavanones	Poriol

Glycosides	Eriocitrin Neoeriocitrin Hesperidin Liquiritin Naringin (Naringenin-7-rutinoside) Narirutin Poncirin Sakuranin

Acetylated	8-Prenylnaringenin Isoxanthohumol Sophoraflavanone G

Acetylated glycosides	Nirurin

v t e Glycosides

Bond	O-glycosidic bond N-glycosidic bond S-glycosidic bond C-glycosidic bond

Geometry	α-Glycoside β-Glycoside 1,4-Glycoside 1,6-Glycoside

Glycone	Fructoside Galactoside Glucoside Glucuronide Rhamnoside Riboside

Aglycone	Alcoholic glycoside Anthraquinone glycoside Cardiac glycoside Bufadienolide Cardenolide Coumarin glycoside Cyanogenic glycoside Flavonoid glycoside Glycosylamine Phenolic glycoside Saponin Steviol glycoside Thioglycoside

Biochemical families: carbohydrates alcohols glycoproteins glycosides lipids eicosanoids fatty acids / intermediates phospholipids sphingolipids steroids nucleic acids constituents / intermediates proteins Amino acids / intermediates tetrapyrroles / intermediates

This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.