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Results for "

Bosutinib

" in MedChemExpress (MCE) Product Catalog:

6

Inhibitors & Agonists

1

Isotope-Labeled Compounds

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-10158
    Bosutinib
    20+ Cited Publications

    SKI-606

    Src Bcr-Abl Autophagy Cancer
    Bosutinib is an orally active Src/Abl tyrosine kinase inhibitor with IC50 of 1.2 nM and 1 nM, respectively .
    Bosutinib
  • HY-10158A
    Bosutinib hydrate
    20+ Cited Publications

    SKI-606 hydrate

    Src Bcr-Abl Cancer
    Bosutinib hydrate is an oraly activel Src/Abl tyrosine kinase inhibito with IC50 of 1.2 nM and 1 nM, respectively .
    Bosutinib hydrate
  • HY-103029

    Wee1 Cancer
    Bosutinib isomer is a ligand or inhibitor with high binding affinity for both Wee1 and Wee2, with Kd values of 43.7 ± 10.0 and 4.7 ± 2.3 nM, respectively .
    Bosutinib isomer
  • HY-10158AR

    SKI-606 (hydrate) (Standard)

    Src Bcr-Abl Cancer
    Bosutinib (Standard) (SKI-606 (Standard)) hydrate is the analytical standard of Bosutinib hydrate (HY-10158A). This product is intended for research and analytical applications. Bosutinib hydrate is an oraly activel Src/Abl tyrosine kinase inhibito with IC50s of 1.2 nM and 1 nM, respectively.
    Bosutinib (hydrate) (Standard)
  • HY-10158S

    SKI-606-d8

    Isotope-Labeled Compounds Src Bcr-Abl Autophagy Cancer
    Bosutinib-d8 is a deuterium labeled Bosutinib. Bosutinib is a dual Src/Abl inhibitor with IC50s of 1.2 nM and 1 nM, respectively[1][2].
    Bosutinib-d8
  • HY-172091

    EGFR Cancer
    CZY43 is a HER3 degrader. CZY43 can effectively induce HER3 degradation in a dose- and time-dependent manner in breast cancer SKBR3 cells. CZY43 potently inhibits HER3-dependent signaling and cancer cell growth and outperforms Bosutinib (HY-10158) .
    CZY43

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