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ChemicalBook--->CAS DataBase List--->314761-14-3

314761-14-3

        314761-14-3 Structure

        314761-14-3 Structure
        IdentificationBack Directory
        [Name]

        BTSA 1
        [CAS]

        314761-14-3
        [Synonyms]

        BTSA 1
        CS-2853
        BTSA 1;BTSA-1
        BTSA1 >=98% (HPLC)
        5-Phenyl-2-(4-phenyl-thiazol-2-yl)-4-(thiazol-2-yl-hydrazono)-2,4-dihydro-pyrazol-3-one
        1H-Pyrazole-4,5-dione, 3-phenyl-1-(4-phenyl-2-thiazolyl)-, 4-[2-(2-thiazolyl)hydrazone]
        [Molecular Formula]

        C21H14N6OS2
        [MOL File]

        314761-14-3.mol
        [Molecular Weight]

        430.51
        Chemical PropertiesBack Directory
        [Boiling point ]

        625.2±48.0 °C(Predicted)
        [density ]

        1.49±0.1 g/cm3(Predicted)
        [storage temp. ]

        Sealed in dry,2-8°C
        [solubility ]

        DMSO:53.0(Max Conc. mg/mL);123.11(Max Conc. mM)
        [form ]

        Solid
        [pka]

        6.52±0.40(Predicted)
        [color ]

        Brown to reddish brown
        Safety DataBack Directory
        [Symbol(GHS) ]


        GHS07
        [Signal word ]

        Warning
        [Hazard statements ]

        H302
        [Precautionary statements ]

        P280-P305+P351+P338
        Spectrum DetailBack Directory
        [Spectrum Detail]

        BTSA 1(314761-14-3)1HNMR
        Hazard InformationBack Directory
        [Biological Activity]

        BTSA1 is a BAX activator that binds to its N-terminal activation site with high affinity and specificity, induces a conformational change in BAX, and causes BAC-mediated apoptosis. It efficiently promotes apoptosis in leukemia cell lines and patient samples without affecting healthy cells.
        [in vivo]

        BTSA1 effectively inhibits human acute myeloid leukemia xenografts and enhances host survival without toxic side effects. In mice, it was well tolerated.
        [target]

        TargetValue
        Bax
        ()
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