Liquiritin
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Liquiritin
structure -
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CAS No:
551-15-5
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Formula:
C21H22O9
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Chemical Name:
Liquiritin
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Synonyms:
4H-1-Benzopyran-4-one,2-[4-(β-D-glucopyranosyloxy)phenyl]-2,3-dihydro-7-hydroxy-,(2S)-;Liquiritin;4H-1-Benzopyran-4-one,2-[4-(β-D-glucopyranosyloxy)phenyl]-2,3-dihydro-7-hydroxy-,(S)-;(2S)-2-[4-(β-D-Glucopyranosyloxy)phenyl]-2,3-dihydro-7-hydroxy-4H-1-benzopyran-4-one;7-Hydroxyflavanone 4′-O-glucoside;Liquiritoside;4′,7-Dihydroxyflavanone 4′-β-D-glucoside;Likviritin;4′,7-Dihydroxyflavanone 4′-β-D-glucopyranoside;Liquiritigenin 4′-β-D-glucopyranoside;17654-21-6;30372-08-8;31564-20-2;100483-53-2;906340-70-3
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CAS No:
Description
Liquiritin is a flavonoid isolated from Glycyrrhiza, acts as an antioxidant and has neuroprotective, anti-cancer and anti-inflammatory activity[1][2].
Liquiritin is a flavanone glycoside that is liquiritigenin attached to a beta-D-glucopyranosyl residue at position 4' via a glycosidic linkage. It has a role as a plant metabolite, an anticoronaviral agent and an anti-inflammatory agent. It is a flavanone glycoside, a beta-D-glucoside, a monosaccharide derivative and a monohydroxyflavanone. It derives from a liquiritigenin.
Characteristics
146
0.4
1.5±0.1 g/cm3
208 °C @ Solvent: Ethanol
746.8°C at 760 mmHg
265.9±26.4 °C
1.670
2-8°C
Computed Properties
Molecular Weight:418.4
XLogP3:0.4
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:4
Exact Mass:418.12638228
Monoisotopic Mass:418.12638228
Topological Polar Surface Area:146
Heavy Atom Count:30
Complexity:593
Defined Atom Stereocenter Count:6
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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