Peucedanol
CAS No. : 46992-81-8
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| Cat. No. : | HY-N3090 |
| M.Wt: | 264.27 |
| Formula: | C14H16O5 |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
Peucedanol is a non-competitive inhibitor of CYP3A4 with a Ki value of 4.07 μM and a competitive inhibitor of CYP1A2 and CYP2D6 with Ki values of 3.39 μM and 6.77 μM, respectively[1]. In Vitro:Peucedanol (0, 2.5, 5, 10, 25, 50, and 100 μM; 0-30 min) is incubated with eight human liver CYP isoforms (CYP1A2, 2A6, 3A4, 2C8, 2C9, 2C19, 2D6, and 2E1), in pooled human liver microsomes (HLMs) for 30 min with specific inhibitors as positive controls.Peucedanol significantly inhibits the activity of CYP1A2, 2D6, and 3A4 in a dose-dependent manner with IC50 values of 6.03 μM, 13.57 μM, and 7.58 μM, respectively[1].
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