Cedrol is a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 µM and 3.4 µM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes.
Molecular Weight:
222.37
Purity:
98.0%
CAS Number:
[77-53-2]
Formula:
C15H26O
Target:
Cytochrome P450 (e.g. CYP17)
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