Peucedanol
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.
For research use only. We do not sell to patients.
- CAS No.: 46992-81-8
- Formula: C14H16O5
- Molecular Weight:264.27
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 46992-81-8
-
Molecular Weight 264.27
-
Formula C14H16O5
-
SMILES
O=C1OC2=C(C=C1)C=C(CC(C(C)(C)O)O)C(O)=C2
-
Structure Classification
-
Initial Source
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)