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31750-48-8

中文名稱 他莫昔芬EP雜質(zhì)F
英文名稱 N-DESMETHYLTAMOXIFEN, HYDROCHLORIDE
CAS 31750-48-8
分子式 C25H27NO
分子量 357.49
MOL 文件 31750-48-8.mol
更新日期 2023/03/20 15:41:27
31750-48-8 結(jié)構(gòu)式 31750-48-8 結(jié)構(gòu)式

基本信息

中文別名
去甲基他莫昔芬
他莫昔芬EP雜質(zhì)F
檸檬酸他莫昔芬EP雜質(zhì)F
英文別名
ici55,548
desmethyltamoxifen
n-desmethyltamoxifen
Tamoxifen EP Impurity F
N-DESMETHYL TAMOXIFEN HCL
N-DEMETHYLTAMOXIFEN, HYDROCHLORIDE
N-DESMETHYLTAMOXIFEN, HYDROCHLORIDE
2-diphenyl-1-butenyl)phenoxy)-n-methyl-2-(p-((z)-ethylamin
2-diphenyl-1-butenyl)phenoxy)-n-methyl-2-(4-((z)-ethanamin
cis-2-(p-(1,2-diphenyl-1-butenyl)phenoxy)-n-methylethylamine

物理化學(xué)性質(zhì)

沸點(diǎn)485.8±33.0 °C(Predicted)
密度1.047±0.06 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度DMSO: 72 mg/mL (201.40 mM);Ethanol: 36 mg/mL (100.70 mM)
酸度系數(shù)(pKa)9.38±0.10(Predicted)
水溶解性水:不溶

安全數(shù)據(jù)

危險(xiǎn)性符號(GHS)GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS07
警示詞危險(xiǎn)
危險(xiǎn)性描述H350-H302-H372-H360
他莫昔芬EP雜質(zhì)F價(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2025/05/22HY-129099A他莫昔芬EP雜質(zhì)F
N-Desmethyltamoxifen hydrochloride
31750-48-81 mg450元
2025/05/22HY-129099A他莫昔芬EP雜質(zhì)F
N-Desmethyltamoxifen hydrochloride
31750-48-810mM * 1mLin DMSO780元
2025/05/22HY-129099A他莫昔芬EP雜質(zhì)F
N-Desmethyltamoxifen hydrochloride
31750-48-85mg900元

常見問題列表

生物活性
N-Desmethyltamoxifen 是 Tamoxifen 在人體內(nèi)的主要代謝產(chǎn)物。N-Desmethyltamoxifen,較弱的抗雌激素,是一種比 Tamoxifen 強(qiáng)十倍的蛋白激酶 C (PKC) 抑制劑。N-Desmethyltamoxifen 也是人體 AML 細(xì)胞神經(jīng)酰胺代謝的有效調(diào)節(jié)因子,限制神經(jīng)酰胺糖基化、水解和鞘氨醇磷酸化。
靶點(diǎn)

PKC

Estrogen Receptor

體外研究

N-desmethyltamoxifen (20-500 ng/ml; 48 hours) has a profound inhibitory effect upon all seven glioma lines (T98G, U87, U138, U373, ALW, AUK, CAS cells).
N-desmethyltamoxifen (1.5-10 μM; 114 hours) inhibits growth of MCF 7 human mammary carcinoma cells.
N-desmethyltamoxifen, resulting from the CYP3A4/5-mediated catalysis of tamoxifen, is the major primary quantitative metabolite of tamoxifen.

Cell Viability Assay

Cell Line: MCF 7 human mammary carcinoma cells
Concentration: 1.5, 2.5, 5, 7.5, 10 μM
Incubation Time: 114 hours
Result: Inhibits growth of MCF 7 human mammary carcinoma cells
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