| Weight | 256.257 g/mol |
|---|---|
| Formula | C15H12O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
isoliquiritigenin (13745-20-5, 961-29-5)
GU-17 · GU 17 · 6'-deoxychalcone
Score:
#1793 in Biochemistry
,
#3918 in Biology
,
#4931 in Chemistry
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- Glabrene and Isoliquiritigenin as Tyrosinase Inhibitors from Licorice Roots (Journal of Agricultural and Food Chemistry, 2003)
- Isoliquiritigenin isolated from the roots of Glycyrrhiza uralensis inhibits LPS-induced iNOS and COX-2 expression via the attenuation of NF-B in RAW 264.7 macrophages (European Journal of Pharmacology, 2008)
- Protective effects of isoliquiritigenin in transient middle cerebral artery occlusion-induced focal cerebral ischemia in rats. (Pharmacological Research, 2006)
- Isoliquiritigenin, a flavonoid from licorice, reduces prostaglandin E2 and nitric oxide, causes apoptosis, and suppresses aberrant crypt foci development (Cancer Science, 2004)
- Estrogenic and antiproliferative activities of isoliquiritigenin in MCF7 breast cancer cells (The Journal of Steroid Biochemistry and Molecular Biology, 2002)
- Inhibition of xanthine oxidase by liquiritigenin and isoliquiritigenin isolated from Sinofranchetia chinensis. (Cellular and Molecular Life Sciences, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - GU-17
- GU 17
- 6'-deoxychalcone
- 2',4',4-trihydroxychalcone
-
SMILESC1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O
-
InChIKeyDXDRHHKMWQZJHT-UHFFFAOYSA-N
- Pubchem - isoliquiritigenin
- Wikipedia - trihydroxychalcone
Isoliquiritigenin is a phenolic chemical compound found in licorice. It is under experimentation phase testing for use as a cancer treatment and as an aide for cocaine addiction. It is a sirtuin-activating compound.
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Synthesis
Reactant
+
4-Hydroxybenzyl chloride
(Wittig)
Reactant
+
4-CHLOROPHENOL
(Stille)
resorcinol
+
Reactant
(Friedel-Crafts acylation)
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isoliquiritigenin
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