A furanocoumarin that inhibits CYP1A
Related Products
Technical Support & Resources

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Isoimperatorin

Item No. 19851

Technical Information
Formal Name
4-[(3-methyl-2-buten-1-yl)oxy]-7H-furo[3,2-g][1]benzopyran-7-one
CAS Number
482-45-1
Molecular Formula
C16H14O4
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMF:PBS (pH 7.2)(1:3): 0.25 mg/mlDMSO: 20 mg/mlEthanol: 10 mg/ml
λmax
221, 250, 259, 268, 309 nm
SMILES
O=C1OC2=C(C(OC/C=C(C)/C)=C(C=CO3)C3=C2)C=C1
InChi Code
InChI=1S/C16H14O4/c1-10(2)5-7-19-16-11-3-4-15(17)20-14(11)9-13-12(16)6-8-18-13/h3-6,8-9H,7H2,1-2H3
InChi Key
IGWDEVSBEKYORK-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Product Description

    Isoimperatorin is a natural furanocoumarin that can be isolated from a variety of plant parts. It inhibits cytochrome P450 (CYP) isoform 1A activity, in particular blocking hepatic ethoxyresorufin O-dealkylase activity.1,2 Through its effects on CYP1A, isoimperatorin reduces the metabolism of polycyclic aromatic hydrocarbons and aflatoxin B1 (Item No. 11293) to reactive metabolites.2,3 Isoimperatorin also induces the expression of glutathione S-transferase α by activating Nrf2.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Cai, Y., Bennett, D., Nair, R.V., et alInhibition and inactivation of murine hepatic ethoxy- and pentoxyresorufin O-dealkylase by naturally occurring coumarins. Chem. Res. Toxicol. 6(6), 872-879 (1993).

    2. Cai, Y., Baer-Dubowska, W., Ashwood-Smith, M., et alInhibitory effects of naturally occurring coumarins on the metabolic activation of benzo[a]pyrene and 7,12-dimethylbenz[a]anthracene in cultured mouse keratinocytes. Carcinogenesis 18(1), 215-222 (1997).

    3. Pokaharel, Y.R., Han, E.H., Kim, J.Y., et alPotent protective effect of isoimperatorin against aflatoxin B1-inducible cytotoxicity in H4IIE cells: Bifunctional effects on glutathione S-transferase and CYP1A. Carcinogenesis 27(12), 2483-2490 (2006).