A furanocoumarin with diverse biological activities
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Isopimpinellin

Item No. 34642

Technical Information
Formal Name
4,9-dimethoxy-7H-furo[3,2-g][1]benzopyran-7-one
CAS Number
482-27-9
Synonyms
  • NSC 217988
  • NSC 401288
Molecular Formula
C13H10O5
Formula Weight
Purity
≥98%
A solid
DMF: 30 mg/mlDMF:PBS (pH 7.2) (1:8): 0.11 mg/mlDMSO: 20 mg/mlEthanol: 1 mg/ml
λmax
223, 241, 249, 272, 312 nm
SMILES
O=C1OC2=C(C=C1)C(OC)=C3C=COC3=C2OC
InChi Code
InChI=1S/C13H10O5/c1-15-10-7-3-4-9(14)18-12(7)13(16-2)11-8(10)5-6-17-11/h3-6H,1-2H3
InChi Key
DFMAXQKDIGCMTL-UHFFFAOYSA-N
Origin
Plant/Saxifraga stolonifera Curt.
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Isopimpinellin is a furanocoumarin that has been found in H. persicum and has diverse biological activities.1,2,3 It inhibits lipid peroxidation in a cell-free assay.1 Isopimpinellin (20 µM) prevents histamine release from, and activation of NF-κB in, RBL-2H3 cells.2 It also decreases the secretion of TNF-α, IL-1β, and IL-4 from RBL-2H3 cells. Isopimpinellin prevents benzo[a]pyrene-DNA adduct formation in sensitivity to carcinogenesis (SENCAR) mice when administered at a dose of 70 mg/kg and reduces the number of papillomas initiated and promoted by 7,12-dimethylbenz[a]anthracene (DMBA; Item No. 30383) in SENCAR mice when administered at 30, 70, or 150 mg/kg.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Souri, E., Farsam, H., Sarkheil, P., et alAntioxidant activity of some furanocoumarins isolated from Heracleum persicum. Pharm. Biol. 42(6), 396-399 (2004).

    2. Li, D., and Wu, L. Coumarins from the roots of Angelica dahurica cause anti-allergic inflammation. Exp. Ther. Med. 14(1), 874-880 (2017).

    3. Kleiner, H.E., Vulimiri, S.V., Starost, M.F., et alOral administration of the citrus coumarin, isopimpinellin, blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[α]anthracene in SENCAR mice. Carcinogenesis 23(10), 1667-1675 (2002).