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ChemicalBook--->CAS DataBase List--->10538-99-5

10538-99-5

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  • 10538-99-5 Structure

    10538-99-5 Structure
    IdentificationBack Directory
    [Name]

    LY 345899)
    [CAS]

    10538-99-5
    [Synonyms]

    LY 345899)
    LY-345899 (LY345899
    L-Glutamic acid, N-[4-(3-amino-1,2,5,6,6a,7-hexahydro-1,9-dioxoimidazo[1,5-f]pteridin-8(9H)-yl)benzoyl]-
    [Molecular Formula]

    C20H21N7O7
    [MDL Number]

    MFCD29920315
    [MOL File]

    10538-99-5.mol
    [Molecular Weight]

    471.42
    Chemical PropertiesBack Directory
    [density ]

    1.82±0.1 g/cm3(Predicted)
    [storage temp. ]

    Store at -20°C
    [solubility ]

    DMSO:125.0(Max Conc. mg/mL);265.16(Max Conc. mM)
    [form ]

    A solid
    [pka]

    3.46±0.10(Predicted)
    [color ]

    Light yellow to yellow
    Safety DataBack Directory
    [Symbol(GHS) ]


    GHS07
    [Signal word ]

    Warning
    [Hazard statements ]

    H302-H312-H332
    [Precautionary statements ]

    P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501
    Hazard InformationBack Directory
    [Biological Activity]

    LY 345899, a folate analog, is also a methylenetetrahydrofolate dehydrogenase (MTHFD1; DC301) and MTHFD2 inhibitor with IC50 values of 96 nM and 663 nM, respectively, and Ki value for MTHFD1 of 18 nM.
    [in vitro]

    LY 345899 could suppress the MTHFD enzyme in the cytoplasm and mitochondria.
    LY 345899 could disturb the NADPH and redox homeostases and accelerate cell death under oxidative stress, such as hypoxia, or causing in vitro anchorage independence and in vivo impaired tumor growth and metastasis.

    [in vivo]

    LY345899 (Intraperitoneal injection; 5-10 mg/kg; 5 d/wk; 4 weeks) shows potent antitumor activity and displays therapeutic activity against CRC in vivo .

    < td class="col1 fwb"> Animal Model: < td class="col1 fwb"> Dosage: table>
    SW620 or PDX-based BABL/c nude colorectal cancer (CRC) model
    5-10 mg/kg
    Administration: Intraperitoneal injection; 5-10 mg/kg; 5 d/wk; 4 weeks
    Result : Displayed lower cell proliferation indices and higher cell apoptosis. Exhibited no statistically significant weight loss or other signs of acute or delayed toxicity in mice.
    [target]

    Ki: 18 nM (MTHFD1); IC50: 96 nM (MTHFD1) and 663 nM (MTHFD2)

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