
CAS Number2657-25-2
SynonymsMFCD00016484; 4'-HYDROXYCHALCONE; HYDROXYCHALCONE,4'; 4′-Hydroxychalcone; 1-(4-Hydroxyphenyl)-3-phenylprop-2-en-1-one
Molecular FormulaC15H12O2
Molecular Weight224.26
Purity97%
Density1.191 g/cm3
Boiling Point419.6ºC at 760 mmHg
Melting Point174-178 °C
AppearanceYellow-cream powder
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 2657-25-2 |
| Catalog No. | 2A-9005883 |
| Chinese Name | 4'-羟基查耳酮 |
| Synonyms | MFCD00016484; 4'-HYDROXYCHALCONE; HYDROXYCHALCONE,4'; 4′-Hydroxychalcone; 1-(4-Hydroxyphenyl)-3-phenylprop-2-en-1-one |
| Molecular Formula | C15H12O2 |
| Molecular Weight | 224.26 |
| Purity | 97 |
| Density | 1.191 g/cm3 |
| Boiling Point | 419.6ºC at 760 mmHg |
| Melting Point | 174-178 °C |
| Appearance | Yellow-cream powder |
| Storage Condition | Sealed in a cool, dry environment |
| Application | 4'-Hydroxychalcone is a chalcone isolated from licorice root and has liver-protective effects. 4'-Hydroxychalcone can inhibit TNFα-induced NF-κB activity by inhibiting the proteasome. 4'-Hydroxychalco |
| MDL Number | MFCD00016484 |
| SMILES | O=C(C=Cc1ccccc1)c1ccc(O)cc1 |
| InChI | InChI=1S/C15H12O2/c16-14-9-7-13(8-10-14)15(17)11-6-12-4-2-1-3-5-12/h1-11,16H/b11-6+ |
| InChI Key | UAHGNXFYLAJDIN-IZZDOVSWSA-N |
| MSDS | msds/5883_1_2657_25_2.pdf |
| Bioactivity | 4'-Hydroxychalcone, a chalcone isolated from licorice root, with hepatoprotective activity. 4'-Hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. 4'-Hydroxychalcone induces a rapid potassium release from mitochondrial vesicles and causes deterioration of respiratory control and oxidative phosphorylation of isolated rat liver mitochondria[1][2][3]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Inoue B, et al. The effects of echinatin and its related compounds on the mitochondrial energy transfer reaction. J Toxicol Sci. 1982 Nov;7(4):245-54. [2]. Ali Reza, et al. Hepatoprotective activity of phloretin and hydroxychalcones against Acetaminophen Induced hepatotoxicity in mice. Iranian Journal of Pharmaceutical Sciences. 2011 Jan; 7(2). [3]. Orlikova B, et al. The aromatic ketone 4'-hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. Biochem Pharmacol. 2011 Sep 15;82(6):620-31. Chemical & Physical Properties Density 1.191 g/cm3 Boiling Point 419.6ºC at 760 mmHg Melting Point 174-178 °C Molecular Formula C15H12O2 Molecular Weight 224.25500 Flash Point 179.1ºC Exact Mass 224.08400 PSA 37.30000 LogP 3.28830 Vapour Pressure 1.23E-07mmHg at 25°C Index of Refraction 1.653 InChIKey UAHGNXFYLAJDIN-IZZDOVSWSA-N SMILES O=C(C=Cc1ccccc1)c1ccc(O)cc1 |
| Use of | 4'-Hydroxychalcone, a chalcone isolated from licorice root, with hepatoprotective activity. 4'-Hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. 4'-Hydroxychalcone induces a rapid potassium release from mitochondrial vesicles and causes deterioration of respiratory control and oxidative phosphorylation of isolated rat liver mitochondria[1][2][3]. Properties Name 4'-hydroxychalcone Synonym More Synonyms 2-Benzal-4-hydroxyacetophenone Biological Activity Description 4'-Hydroxychalcone, a chalcone isolated from licorice root, with hepatoprotective activity. 4'-Hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. 4'-Hydroxychalcone induces a rapid potassium release from mitochondrial vesicles and causes deterioration of respiratory control and oxidative phosphorylation of isolated rat liver mitochondria[1][2][3]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Inoue B, et al. The effects of echinatin and its related compounds on the mitochondrial energy transfer reaction. J Toxicol Sci. 1982 Nov;7(4):245-54. [2]. Ali Reza, et al. Hepatoprotective activity of phloretin and hydroxychalcones against Acetaminophen Induced hepatotoxicity in mice. Iranian Journal of Pharmaceutical Sciences. 2011 Jan; 7(2). [3]. Orlikova B, et al. The aromatic ketone 4'-hydroxychalcone inhibits TNFα-induced NF-κB activation via proteasome inhibition. Biochem Pharmacol. 2011 Sep 15;82(6):620-31. Chemical & Physical Properties Molecular Formula C15H12O2 Exact Mass 224.08400 PSA 37.30000 LogP 3.28830 Index of Refraction 1.653 InChIKey UAHGNXFYLAJDIN-IZZDOVSWSA-N |
| Transport Info | Product name: Purity: 98.0% |
| MSDS Transport Info | Module 14. Shipping information United Nations classification: inconsistent with United Nations classification standards UN number: not specified 4'-Hydroxychalcone Modification Number: 5 |
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