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    常州市存仁生物工程有限公司

    SNX5422

    SNX5422

    Description of:SNX5422
    PF-04929113 (SNX-5422) is a synthetic prodrug targeting the human heat-shock protein 90 (Hsp90) with potential antineopl...
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    MPC3100

    MPC3100

    Description of:MPC3100
    MPC-3100 is an orally bioavailable, synthetic, second-generation small-molecule inhibitor of heat shock protein 90 (Hs...
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    17-AAG(Tanespimycin)

    17-AAG(Tanespimycin)

    Description of:17-AAG(Tanespimycin)
    17AAG is a less toxic analogue of the geldanamycin which binds to Hsp90 (Heat Shock Protein 90) and alters ...
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    BIIB021

    BIIB021

    Description of:BIIB021
    In tumor cells, BIIB021 induced the degradation of Hsp90 client proteins (including HER-2, AKT, and Raf-1) and up-regula...
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    SNX-2112

    SNX-2112

    Description of:SNX-2112
    SNX-2112 is an active metabolite of the compounds SNX-5542. SNX-2112 is rapidly transformed form SNX-5542 after adminis...
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    NVP-AUY922

    NVP-AUY922

    Description of:NVP-AUY922
    NVP-AUY922, a novel resorcinylic isoxazole amide heat shock protein 90 (HSP90) inhibitor. NVP-AUY922 potently inhibit...
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    NVP-BEP800

    NVP-BEP800

    Description of:NVP-BEP800
    NVP-BEP800 is a novel, fully synthetic, oral Hsp90 inhibitor with an IC50 of 0.058 ± 0.006 μM.
    The...
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    Geldanamycin

    Geldanamycin

    Description of:Geldanamycin
    Geldanamycin,Binds to the ATP site of Hsp90 (Kd = 1.2 μM) and inhibits its chaperone activity. Consequently inhi...
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