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ChemicalBook--->CAS DataBase List--->292618-32-7

292618-32-7

        292618-32-7 Structure

        292618-32-7 Structure
        IdentificationBack Directory
        [Name]

        ST1481
        [CAS]

        292618-32-7
        [Synonyms]

        ST1481
        Lbq707
        CPT 184
        GIMATECAN
        Unii-7kks9R192f
        ST1481: GIMATECAN
        LBQ707; ST1481; CPT 184
        7-T-Butoxyiminomethylcamptothecin
        7-[(E)-tert-butyloxyiminomethyl]-camptothecin
        (4S)-11-((E)-((1,1-Dimethylethoxy)imino)methyl)-4-ethyl-4-hydroxy-1,12-dihydro-14H-pyrano(3',4':6,7)indolizino(1,2-b)quinoline-3,14(4H)-dione
        1H-Pyrano(3',4':6,7)indolizino(1,2-B)quinoline-11-carboxaldehyde, 4-ethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-, 11-(o-(1,1-dimethylethyl)oxime), (C(E),4S)-
        [Molecular Formula]

        C25H25N3O5
        [MDL Number]

        MFCD06795143
        [MOL File]

        292618-32-7.mol
        [Molecular Weight]

        447.49
        Chemical PropertiesBack Directory
        [Boiling point ]

        780.6±70.0 °C(Predicted)
        [density ]

        1.37±0.1 g/cm3(Predicted)
        [storage temp. ]

        Store at -20°C
        [form ]

        Solid
        [pka]

        11.20±0.20(Predicted)
        [color ]

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


        GHS07,GHS08,GHS06
        [Signal word ]

        Danger
        [Hazard statements ]

        H300-H335-H319-H351-H315
        [Precautionary statements ]

        P201-P202-P281-P308+P313-P405-P501-P264-P270-P301+P310-P321-P330-P405-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
        Spectrum DetailBack Directory
        [Spectrum Detail]

        ST1481(292618-32-7)1HNMR
        Hazard InformationBack Directory
        [Biological Activity]

        Gimatecan (ST1481) is a potent topoisomerase I inhibitor. It is an orally active camptothecin analog with antineoplastic activity.
        [in vivo]

        Gimatecan (2 mg/kg; treatment per os, every fourth day for four times) is effective for inhibiting tumor growth.

        < div class="cpd-mod-vv">
        table>
        Animal Model: Athymic Swiss nude mice bearing HT1376 model
        Dosage: 2 mg/kg
        Administration: Treatment per os, every fourth day for four times
        Result: Caused a marked tumor growth inhibition during treatment.
        [target]

        Topoisomerase I

        [storage]

        Store at -20°C
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