1. Metabolic Enzyme/Protease
  2. Cytochrome P450
  3. DL-Acetylshikonin

DL-Acetylshikonin is a non-selective, reversible cytochrome P450 inhibitor with IC50 values of 1.4-4.0 μM. DL-Acetylshikonin has anti-cancer and anti-inflammatory activities.

For research use only. We do not sell to patients.

DL-Acetylshikonin Chemical Structure

DL-Acetylshikonin Chemical Structure

CAS No. : 54984-93-9

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Description

DL-Acetylshikonin is a non-selective, reversible cytochrome P450 inhibitor with IC50 values of 1.4-4.0 μM. DL-Acetylshikonin has anti-cancer and anti-inflammatory activities[1].

IC50 & Target[1]

CYP2C8

1.4 μM (IC50)

CYP2B6

2.0 μM (IC50)

CYP3A

2.3 μM (IC50)

CYP2C19

2.5 μM (IC50)

CYP2D6

2.5 μM (IC50)

CYP2E1

2.7 μM (IC50)

CYP2C9

3.3 μM (IC50)

CYP2J2

3.3 μM (IC50)

CYP2A6

3.8 μM (IC50)

CYP1A2

4.0 μM (IC50)

In Vitro

DL-Acetylshikonin inhibits CYP3A-mediated testosterone and Nifedipine (HY-B0284) metabolism with IC50 values of 5.2 μM and 3.0 μM, respectively, indicating that it inhibits CYP3A activity in a substrate-independent manner[1].
DL-Acetylshikonin is not a time-dependent inhibitor[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

330.33

Formula

C18H18O6

CAS No.
SMILES

C/C(C)=C\CC(OC(C)=O)C1=CC(C2=C(O)C=CC(O)=C2C1=O)=O

Structure Classification
Initial Source
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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
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
DL-Acetylshikonin
Cat. No.:
HY-N2181A
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