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Isoliquiritin

  Cat. No.:  DC23110   Featured
Chemical Structure
5041-81-6
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More than 5000 active chemicals with high quality for research!
Field of application
Isoliquiritin has significant antidepressant-like, antifungal and anti-cancer activities. It induces apoptotic cell death through upregulating p53 and p21 in the A549 non-small cell lung cancer cells and inhibit the p53-dependent pathway and showed crosst
Cas No.: 5041-81-6
Chemical Name: Isoliquiritin
Synonyms: ISOLIQUIRITIN;(E)-1-(2,4-Dihydroxyphenyl)-3-[4-(β-D-glucopyranosyloxy)phenyl]-2-propen-1-one;[(E)-2',4'-Dihydroxychalcone-4-yl]β-D-glucopyranoside;2-Propen-1-one, 1-(2,4-dihydroxyphenyl)-3-[4-(.beta.-D-glucopyranosyloxy)phenyl]-, (2E)-;Aids004475;Aids-004475;neoisoliquritin;2',4,4'-Trihydroxychalcone 4-(beta-D-glucopyranoside);(E)-1-(2,4-dihydroxyphenyl)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one;4-[(1E)-3-(2,4-dihydroxyphenyl)-3-oxoprop-1-en-1-yl]phenyl beta-D-glucopyranoside;2′,4,4′-Trihydroxychalcone 4-glucoside;Isoliquiritoside;2',4,4'-Trihydroxychalcone 4-beta-D-glucopyranoside;2Y348H1V4W;MEGxp0_001945;YNWXJFQOCHMPCK-LXGDFETPSA-N;LMPK12120021;BDBM50362885;X1167;N1750;X1193;C16978;I07-
SMILES: O1[C@]([H])([C@@]([H])([C@]([H])([C@@]([H])([C@@]1([H])C([H])([H])O[H])O[H])O[H])O[H])OC1C([H])=C([H])C(/C(/[H])=C(\[H])/C(C2C([H])=C([H])C(=C([H])C=2O[H])O[H])=O)=C([H])C=1[H]
Formula: C21H22O9
M.Wt: 418.3940
Purity: >98%, Standard References Grade
Sotrage: 4°C for 1 year, -20°C for more than 2 years
Description: Isoliquiritin, isolated from Licorice Root, inhibits angiogenesis and tube formation. Isoliquiritin also exhibits antidepressant-like effects and antifungal activity[1][2][3].
References: [1]. Kobayashi S, et al. Inhibitory effect of isoliquiritin, a compound in licorice root, on angiogenesis in vivo and tube formation in vitro. Biol Pharm Bull. 1995 Oct;18(10):1382-6. [2]. Wang W, et al. Antidepressant-like effects of liquiritin and isoliquiritin from Glycyrrhiza uralensis in the forced swimming test and tail suspension test in mice. Prog Neuropsychopharmacol Biol Psychiatry. 2008 Jul 1;32(5):1179-84. [3]. Luo J, et al. Antifungal Activity of Isoliquiritin and Its Inhibitory Effect against Peronophythora litchi Chen through a Membrane Damage Mechanism. Molecules. 2016 Feb 19;21(2):237.
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