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PROTAC D16-M1P2

PROTAC D16-M1P2 is an orally active PKMYT1 PROTAC degrader with a DC50 of 0.7 nM. PROTAC D16-M1P2 also inhibits the activity of PKMYT1 with an IC50 of 7.6 nM. PROTAC D16-M1P2 inhibits pCDK1 with an IC50 of 9 nM. PROTAC D16-M1P2 has demonstrated significant anti-tumor efficacy in mouse models and can be used for research on breast cancer.

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  • 分子式: C43H45FN10O4
  • 分子量:784.88
  • 保管条件:

    Please store the product under the recommended conditions in the Certificate of Analysis.

  • PROTAC D16-M1P2 Chemical Structure
    PROTAC D16-M1P2 構造式
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最寄りの代理店をお探しください Your local distributor: Hycultec GmbHHycultec
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100 mg

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  • PROTAC D16-M1P2 Chemical Structure
    PROTAC D16-M1P2 Chemical Structure
    1/16
  • PROTAC D16-M1P2