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.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 46992-81-8
- 分子式: C14H16O5
- 分子量:264.27
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保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性
製品説明
体外実験
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.
化学情報
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CAS 番号 46992-81-8
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分子量 264.27
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分子式 C14H16O5
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SMILES
O=C1OC2=C(C=C1)C=C(CC(C(C)(C)O)O)C(O)=C2
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Structure Classification
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Initial Source
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)