Phthalazinone pyrazole is a potent, selective, and orally active inhibitor of Aurora-A kinase with an IC50 of 0.031 µM. Phthalazinone pyrazole can arrests mitosis and subsequently inhibit tumor growth via apoptosis of proliferating cells. Phthalazinone pyrazole suppresses the epithelial-mesenchymal transition (EMT) during the differentiation of hepatocyte-like cells (HLCs) from human embryonic stem cells[1][2].
Molecular Weight:
317.34
Purity:
98
CAS Number:
[880487-62-7]
Formula:
C18H15N5O
Target:
Apoptosis,Aurora Kinase,Mitosis
Application Notes:
MCE Product type: Reference compound
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