ARTEMISININ

ARTEMISININ Basic information
Product Name:ARTEMISININ
Synonyms:4’-methylkaempferol;Kaempferide~3,5,7-Trihydroxy-4-methoxyflavone;3,5,7-trihydroxy-2-(4-methoxyphenyl)-4-benzopyrone;Kaemperide;3,5,7-Trihydroxy-2-(4-methoxy-phenyl)-chromen-4-;ARTEMISIA P E;ARTEMISINE;ARTEMISININE
CAS:491-54-3
MF:C16H12O6
MW:300.26
EINECS:207-738-4
Product Categories:Flavanols;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract
Mol File:491-54-3.mol
ARTEMISININ Structure
ARTEMISININ Chemical Properties
Melting point 156-157 °C(lit.)
Boiling point 543.8±50.0 °C(Predicted)
density 1.538
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Chloroform (Slightly, Heated), DMSO (Slightly, Heated), Methanol (Slightly, Heat
form neat
pka6.32±0.40(Predicted)
color Yellow
BRN 305378
LogP2.740 (est)
CAS DataBase Reference491-54-3
Safety Information
Safety Statements 24/25
WGK Germany 2
RTECS KD4170000
HS Code 29329990
MSDS Information
ProviderLanguage
SigmaAldrich English
ARTEMISININ Usage And Synthesis
Chemical PropertiesYellow powder
UsesKaempferide is a flavonoid that maintains anti-radical and anti-oxidant capabilities, as well as anti-tumour possibilities. Impurity of Icaritin (I163700).
DefinitionChEBI: A monomethoxyflavone that is the 4'-O-methyl derivative of kaempferol.
Biological Activitythe effects of phytoestrogens have been studied in the hypothalamic-pituitary-gonadal axis and various non-gonadal targets. epidemiologic and experimental evidence indicates a protective effect of phytoestrogens also in colorectal cancer. the mechanism through which estrogenic molecules control colorectal cancer tumorigenesis could possibly involve estrogen receptor β, which is the predominantly expressed estrogen receptor subtype in colon mucosa.
in vitrokaempferide triglycoside proved to inhibit the proliferation of native and estrogen receptor β overexpressing colon cancer cells via a mechanism not mediated by ligand binding dependent estrogen receptor activation. it affected hct8 cell cycle progression through increasing the g0/g1 cell fraction and in estrogen receptor β overexpressing cells increased two antioxidant enzymes [1].
in vivothe aim of one previous study was to evaluate the effect of kaempferol on tissue lipid peroxidation and antioxidant status in 1,2-dimethyl hydrazine induced colorectal cancer in male wistar rats and to compare its efficacy with irinotecan. this study revealed that kaempferol could be safely used as a chemopreventive agent in colorectal cancer [2].
references[1] martineti v, tognarini i, azzari c, carbonell sala s, clematis f, dolci m, lanzotti v, tonelli f, brandi ml, curir p. inhibition of in vitro growth and arrest in the g0/g1 phase of hct8 line human colon cancer cells by kaempferide triglycoside from dianthus caryophyllus. phytother res. 2010 sep;24(9):1302-8.
[2] nirmala p, ramanathan m. effect of kaempferol on lipid peroxidation and antioxidant status in 1,2-dimethyl hydrazine induced colorectal carcinoma in rats. eur j pharmacol. 2011 mar 1;654(1):75-9.
ARTEMISININ Preparation Products And Raw materials
Arteannuin-d3 3,4'-DIMETHOXY-3',5,7-TRIHYDROXYFLAVONE 3,7,3',4'-TETRAMETHYLGOSSYPETIN Artemisinin (Arteannuin, Qinghaosu, Qing Hau Sau) 5,7-DIHYDROXY-3-METHOXY-2-(4-METHOXY-PHENYL)-CHROMEN-4-ONE Ombuoside arteannuin B 3,3',4',5,6,7,8-heptamethoxyflavone TAMARIXETIN-7-O-RUTINOSIDE 3,4-DIMETHOXY-3,5,7-TRIHYDROXYFLAVONE KAEMPFEROL-3,7,4'-TRIMETHYL ETHER QUERCETIN-3,4'-DI-O-GLUCOSIDE 3,5,7-TRIHYDROXY-3',4',5'-TRIMETHOXYFLAVONE 4',7-DIMETHOXY-3,3',5-TRIHYDROXYFLAVONE Artemisinin/arteannuin QUERCETIN-3,7,3',4'-TETRAMETHYL ETHER 3,5-DIHYDROXY-7-METHOXY-2-(4-METHOXY-PHENYL)-CHROMEN-4-ONE QUERCETINPENTAACETATE

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