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ChemicalBook--->CAS DataBase List--->31750-48-8

31750-48-8

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    31750-48-8 Structure

    31750-48-8 Structure
    IdentificationBack Directory
    [Name]

    N-DESMETHYLTAMOXIFEN, HYDROCHLORIDE
    [CAS]

    31750-48-8
    [Synonyms]

    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-(4-((z)-ethanamin
    2-diphenyl-1-butenyl)phenoxy)-n-methyl-2-(p-((z)-ethylamin
    cis-2-(p-(1,2-diphenyl-1-butenyl)phenoxy)-n-methylethylamine
    (Z)-2-[4-(1,2-DIPHENYL-1-BUTENYL)PHENOXY]-N-METHYL-ETHANAMINE
    (Z)-2-(4-(1,2-diphenylbut-1-en-1-yl)phenoxy)-N-methylethanamine
    Ethanamine, 2-[4-[(1Z)-1,2-diphenyl-1-buten-1-yl]phenoxy]-N-methyl-
    2-[4-[(1Z)-1,2-Diphenyl-1-buten-1-yl]phenoxy]-N-methylethanamine HCl
    [Molecular Formula]

    C25H27NO
    [MDL Number]

    MFCD03423594
    [MOL File]

    31750-48-8.mol
    [Molecular Weight]

    357.49
    Chemical PropertiesBack Directory
    [Boiling point ]

    485.8±33.0 °C(Predicted)
    [density ]

    1.047±0.06 g/cm3(Predicted)
    [storage temp. ]

    Store at -20°C
    [solubility ]

    DMSO: 72 mg/mL (201.40 mM);Ethanol: 36 mg/mL (100.70 mM)
    [pka]

    9.38±0.10(Predicted)
    [Water Solubility ]

    Water: Insoluble
    Safety DataBack Directory
    [Symbol(GHS) ]


    GHS08,GHS07
    [Signal word ]

    Danger
    [Hazard statements ]

    H350-H302-H372-H360
    [Precautionary statements ]

    P264-P270-P301+P312-P330-P501-P260-P264-P270-P314-P501
    Hazard InformationBack Directory
    [Definition]

    ChEBI: N-Desmethyltamoxifen is a stilbenoid.
    [Biological Activity]

    N-Desmethyltamoxifen is the main metabolite of Tamoxifen in the human body. N-Desmethyltamoxifen, a weaker antiestrogen, is a protein kinase C (PKC) inhibitor ten times stronger than Tamoxifen. It is also a potent regulator of ceramide metabolism in human AML cells, limiting ceramide glycosylation, hydrolysis and sphingosine phosphorylation.
    [in vitro]

    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).
    It 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

    td>
    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
    [target]

    < /table>

    PKC

    Estrogen Receptor

    [storage]

    Store at -20°C
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    Tags:31750-48-8 Related Product Information
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