WWZ-11-098 is a selective CDK6 PROTAC degrader with DC50 of 2.6 nM. WWZ-11-098 induces degradation of CDK6 in a CRBN-dependent manner, while sparing CDK1, CDK2, CDK4, and CDK9. WWZ-11-098 induces apoptosis, G1-S cell cycle arrest and shows anti-proliferative activity in cancer cells. WWZ-11-098 exhibits antitumor efficacy in a xenograft model without signs of toxicity. WWZ-11-098 can be used for the research of leukemia[1].
Molekulargewicht:
828.90
Formel:
C39H47F3N8O7S
Target-Kategorie:
Apoptosis,CDK,PROTACs
Anwendungsbeschreibung:
MCE Product type: Reference compound
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