RP-1664 is a selective and orally active PLK4 inhibitor with an IC50 of 3 nM. RP-1664 demonstrates exquisite selectivity over related kinases, including AURKA/B and PLK1. RP-1664 disrupts centriole biogenesis in cancer cells and leads an accumulation of PLK4 and p21 protein. RP-1664 demonstrates increased sensitivity in TRIM37-high-expressing cells or tumors. RP-1664 exhibits anti-tumor activity in breast cancer and neuroblastoma research[1][2].
Molekulargewicht:
514.55
Reinheit:
98.77
CAS Nummer:
[2980682-00-4]
Formel:
C23H24F2N8O2S
Target-Kategorie:
Polo-like Kinase (PLK)
Anwendungsbeschreibung:
MCE Product type: Reference compound
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