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ChemicalBook--->CAS DataBase List--->2328073-61-4

2328073-61-4

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      1. 2328073-61-4 Structure

        2328073-61-4 Structure
        IdentificationBack Directory
        [Name]

        ZT-12-037-01
        [CAS]

        2328073-61-4
        [Synonyms]

        ZT-12-037-01
        2,4-Quinazolinediamine, N2-cyclopropyl-6,7-dimethoxy-N4-[1-(1-methylethyl)-4-piperidinyl]-
        [Molecular Formula]

        C21H31N5O2
        [MDL Number]

        MFCD32197197
        [MOL File]

        2328073-61-4.mol
        [Molecular Weight]

        385.5
        Chemical PropertiesBack Directory
        [storage temp. ]

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

        DMSO: 8.33 mg/mL (21.61 mM)
        [form ]

        Solid
        [color ]

        White to off-white
        Safety DataBack Directory
        [Symbol(GHS) ]


        GHS07
        [Signal word ]

        Warning
        [Hazard statements ]

        H302-H315-H319-H335
        [Precautionary statements ]

        P261-P280-P301+P312-P302+P352-P305+P351+P338
        Spectrum DetailBack Directory
        [Spectrum Detail]

        ZT-12-037-01(2328073-61-4)1HNMR
        Hazard InformationBack Directory
        [Biological Activity]

        ZT-12-037-01 is an ATP-competitive STK19 inhibitor with IC50 values of 23.96 nM and 27.94 nM for STK19 (WT) and STK19 (D89N), respectively. At a concentration of 1 μM, it is highly selective against a kinase library of 468 kinases.
        [in vitro]

        Treatment with ZT-12-037-01 could effectively inhibit NRAS phosphorylation. ZT-12-037-01 is an ATP-competitive inhibitor that potently inhibits melanocytic colony formation, proliferation and tumor formation driven by mutant NRAS-STK19. It's pro-apoptotic activity was significantly enhanced in cells expressing oncogenic NRAS.

        [in vivo]

        ZT-12-037-01 is a potent STK19 inhibitor with low toxicity in vivo. In the SK-MEL-2 xenograft model (carrying NRAS.

        [target]

        < /table>
        TargetValue
        STK19
        (Cell-free assay)
        23.96 nM
        STK19 (D89N)
        (Cell-free assay)
        27.94 nM
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