| Identification | More | [Name]
2-HYDROXYCHALCONE | [CAS]
644-78-0 | [Synonyms]
2-(2-HYDROXYBENZAL)ACETOPHENONE
2-(2-HYDROXYBENZYLIDENE)ACETOPHENONE
2-HYDROXYBENZYLIDENE ACETOPHENONE
2-HYDROXYCHALCONE
BENZYLIDENE-2-HYDROXYACETOPHENONE
(E)-3-(2-HYDROXYPHENYL)-1-PHENYLPROP-2-EN-1-ONE
HYDROXYCHALCONE, 2-
SALICYLALACETOPHENONE
TRANS-2-HYDROXYBENZYLIDENEACETOPHENONE
TRANS-2-HYDROXYCHALCONE
(2-Hydroxybenzylidene)acetophenone~3-(2-Hydroxyphenyl)-1-phenyl-2-propen-1-one
2-Hydroxychalcone, 98+%
3-(2-hydroxyphenyl)-1-phenyl-2-propen-1-one
2-HYDROXYCHALCONE(UNSPECIFIEDISOMER)
3-(2-hydroxyphenyl)-1-phenylprop-2-en-1-one
o-Hydroxychalcone
α-(o-Hydroxybenzylidene)acetophenone | [EINECS(EC#)]
211-422-1 | [Molecular Formula]
C15H12O2 | [MDL Number]
MFCD00016449 | [Molecular Weight]
224.25 | [MOL File]
644-78-0.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [HS Code ]
29147000 |
| Hazard Information | Back Directory | [Description]
2-hydroxychalcone, a natural flavonoid, is a potent antioxidant, inhibiting lipid peroxidation. It is also capable of inducing apoptosis by downregulating Bcl-2 levels and inhibiting the activation of NF-kB. | [Uses]
2-hydroxychalcone, a natural flavonoid, is a potent antioxidant, inhibiting lipid peroxidation. 2-Hydroxychalcone induces apoptosis by Bcl-2 downregulation. 2-Hydroxychalcone inhibits the activation of NF-kB[1][2][3]. | [Synthesis]
A synthesis of 2-Hydroxychalcone was conducted using acetophenone and o-hydroxybenzaldehyde as starting materials. The reaction was catalyzed by potassium hydroxide and ethanol was used as the solvent. | [in vitro]
2-Hydroxychalcone inhibits invasion of triple negative breast cancer cells.
2-hydroxychalcone inhibits the adhesion of peripheral neutrophils to the endothelial cell monolayers by inhibiting the expression of ICAM-1, VCAM-1, and E-selectin in a concentration-dependent manner. | [References]
[1]. Sun Young Kim, et al. 2-Hydroxychalcone and Xanthohumol Inhibit Invasion of Triple Negative Breast Cancer Cells. Chem Biol Interact. 2013 May 25;203(3):565-72. DOI:10.1016/j.cbi.2013.03.012
[2]. B Madan, et al. 2'-hydroxychalcone Inhibits Nuclear factor-kappaB and Blocks Tumor Necrosis Factor-Alpha- And Lipopolysaccharide-Induced Adhesion of Neutrophils to Human Umbilical Vein Endothelial Cells. Mol Pharmacol. 2000 Sep;58(3):526-34. DOI:10.1124/MOL.58.3.526
[3]. Sonochemical Synthesis of 2’-Hydroxy-Chalcone Derivatives with Potential Anti-Oomycete Activity doi: 10.3390/antibiotics9090576 |
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| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
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| Telephone: |
400-6106006 |
| Website: |
http://chemicals.thermofisher.cn |
| Company Name: |
Energy Chemical
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| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
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