2-TrifluoroMethyl-2'-Methoxychalcone

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CAS:1309371-03-6
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CAS:1309371-03-6
Purity:98% Package:1G;10G;100G Remarks:2-Trifluoromethyl-2'-methoxychalcone is a potent activator of Nrf2. Nrf2 activation is central to cytoprotective gene expression against oxidative and/or electrophilic stress.
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Products Intro: Product Name:2-TrifluoroMethyl-2-Methoxychalcone
CAS:1309371-03-6
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2-TrifluoroMethyl-2'-Methoxychalcone Basic information
Product Name:2-TrifluoroMethyl-2'-Methoxychalcone
Synonyms:2-TrifluoroMethyl-2'-Methoxychalcone;2-Propen-1-one, 1-(2-methoxyphenyl)-3-[2-(trifluoromethyl)phenyl]-, (2E)-;(2E)-1-(2-Methoxyphenyl)-3-[2-(trifluoromethyl)phenyl]-2-propen-1-one;2-Trifluoromethyl-2'-methoxychalcone
CAS:1309371-03-6
MF:C17H13F3O2
MW:306.28
EINECS:
Product Categories:Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:1309371-03-6.mol
2-TrifluoroMethyl-2'-Methoxychalcone Structure
2-TrifluoroMethyl-2'-Methoxychalcone Chemical Properties
Boiling point 395.6±42.0 °C(Predicted)
density 1.238±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility ≤11mg/ml in ethanol;5mg/ml in DMSO;14mg/ml in dimethyl formamide
form solution in acetate.
Safety Information
MSDS Information
2-TrifluoroMethyl-2'-Methoxychalcone Usage And Synthesis
Uses2-Trifluoromethyl-2''-methoxychalcone is a novel chalcone derivative as potent Nrf2 activators in mice and human lung epithelial cells. 2-Trifluoromethyl-2''-methoxychalcone is a potent activator of Nrf2, both, in vitro and in mice. 4 Human bronchial epithelial cells treated with 10 μM 2-trifluoromethyl-2''-methoxychalcone showed a marked increase in the expression of the Nrf2-regulated antioxidant genes, GCLM and NQO1.
UsesNrf2 activation is central to cytoprotective gene expression against oxidative and/or electrophilic stress. Unless activated by inflammatory, environmental, or oxidative stressors, Nrf2 is sequestered in the cytoplasm by its repressor, Keap1. Because of its protective capabilities, small molecules that activate Nrf2 signaling are being examined as potential anti-cancer or anti-inflammatory agents. 2-Trifluoromethyl-2'-methoxychalcone is a potent activator of Nrf2, both in vitro and in mice. Human bronchial epithelial cells treated with 10 μM 2-trifluoromethyl-2'-methoxychalcone showed a marked increase in the expression of the Nrf2-regulated antioxidant genes, GCLM and NQO1. Furthermore, treatment of mice mice with 50 mg/kg 2-trifluoromethyl-2’-methoxychalcone leads to a 4.5- and 4.6-fold increase in the expression of GCLM and NQO1, respectively, in the small intestine compared to controls.[Cayman Chemical]
Uses2-Trifluoromethyl-2'-methoxychalcone is a novel chalcone derivative as potent Nrf2 activators in mice and human lung epithelial cells. 2-Trifluoromethyl-2'-methoxychalcone is a potent activator of Nrf2, both, in vitro and in mice. 4 Human bronchial epithelial cells treated with 10 μM 2-trifluoromethyl-2'-methoxychalcone showed a marked increase in the expression of the Nrf2-regulated antioxidant genes, GCLM and NQO1.
Biological Activity2-trifluoromethyl-2'-methoxychalcone is a nrf2 activator.nrf2-mediated activation of antioxidant response element is a key process of molecular mechanisms regulating the protective function of phase ii detoxification and antioxidant enzymes against oxidative stress, carcinogenesis, and inflammation.
in vitrothe expression of luciferase gene under the control of nqo1-are sequence was measured using stably transfected beas-2b cells treated with 2-trifluoromethyl-2'-methoxychalcone. results showed that the exposure to 2-trifluoromethyl-2'-methoxychalcone led to a significant concentration-dependent increase in luciferase activity. moreover, beas-2b cells were coincubated with 2-trifluoromethyl-2'-methoxychalcone and with or without n-acetylcysteine, and it was found that 2-trifluoromethyl-2'-methoxychalcone could potentially increase the expression of nr2-regulated antioxidant genes in the presence of n-acetylcysteine [1].
in vivoc57bl/6 mice were treated with a single dose of vehicle or 2-trifluoromethyl-2'-methoxychalcone or sulforaphane as the positive control, and small intestines were harvested 24 h later. results showed that the expression of gclm and nqo1 in the small intestine of mice treated with 2-trifluoromethyl-2'-methoxychalcone was 6-fold and 10-fold higher compared to vehicle, respectively. in addition, the expression of gclm and nqo1 in the small intestine treated with 2-trifluoromethyl-2'-methoxychalcone was 3-fold and 5-fold higher compared to sulforaphane, respectively [1].
references[1] v. kumar, s. kumar, m. hassan, et al. novel chalcone derivatives as potent nrf2 activators in mice and human lung epithelial cells. journal of medicinal chemistry 54(12), 4147-4159 (2011).
2-TrifluoroMethyl-2'-Methoxychalcone Preparation Products And Raw materials
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