Cloperidone is an inhibitor for cytochrome P450 2C9 (CYP2C9) with an IC50 of 17.7 µM. Cloperidone exhibits cytotoxicity on HepG2 cells expressing CYP2C9 (60% survival rate at 10 µM)[1].
Molecular Weight:
398.89
CAS Number:
[4052-13-5]
Formula:
C21H23ClN4O2
Target:
Cytochrome P450
Application Notes:
MCE Product type: Oligonucleotides
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