A natural flavone with diverse biological activities
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Isomer(s)
15246Fisetin
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Scutellarein

Item No. 24977

Technical Information
Formal Name
5,6,7-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
CAS Number
529-53-3
Synonyms
  • 6-Hydroxyapigenin
Molecular Formula
C15H10O6
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 20 mg/mlDMSO: 20 mg/mlDMSO:PBS (pH 7.2) (1:1): 0.5 mg/mlEthanol: 0.2 mg/ml
λmax
219, 338 nm
SMILES
OC1=C(O)C(O)=C(C(C=C(C2=CC=C(O)C=C2)O3)=O)C3=C1
InChi Code
InChI=1S/C15H10O6/c16-8-3-1-7(2-4-8)11-5-9(17)13-12(21-11)6-10(18)14(19)15(13)20/h1-6,16,18-20H
InChi Key
JVXZRQGOGOXCEC-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Scutellarein is a flavone that has been isolated from S. baicalensis and has antioxidant, enzyme inhibitory, anti-inflammatory, and antiproliferative biological activities.1,2,3,4,5,6 It has antioxidant activity in a total reactive antioxidant potential (TRAP) assay when used at a concentration of 1 μg/ml.2 Scutellarein inhibits sucrose hydrolysis by rat intestinal α-glucosidase and ATPase activity of the severe acute respiratory syndrome (SARS) coronavirus helicase nsP13 (IC50s = 12 and 0.86 μM, respectively).3,4 It decreases nitric oxide (NO) release and mRNA expression of inducible NO synthase (iNOS) and TNF-α induced by LPS in RAW 264.7 macrophages when used at a concentration of 50 μM.5 In vivo, scutellarein (0.5 μg/g) decreases tumor weight and volume in an HT-1080 human fibrosarcoma mouse xenograft model.6

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Hui, K.M., Wang, X.H., and Xue, H. Interaction of flavones from the roots of Scutellaria baicalensis with the benzodiazepine site. Planta Med. 66(1), 91-93 (2000).

    2. Siraichi, J.T.G., Felipe, D.F., Brambilla, L.Z.S., et alAntioxidant capacity of the leaf extract obtained from Arrabidaea chica cultivated in Southern Brazil. PLoS One 8(8), e72733 (2013).

    3. Kawabata, J., Mizuhata, K., Sato, E., et al6-Hydroxyflavonoids as α-glucosidase inhibitors from marjoram (Origanum majorana) leaves. Biosci. Biotechnol. Biochem. 67(2), 445-447 (2003).

    4. Yu, M.-S., Lee, J., Lee, J.M., et alIdentification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13. Bioorg. Med. Chem. Lett. 22(12), 4049-4054 (2012).

    5. Sung, N.Y., Kim, M.-Y., and Cho, J.Y. Scutellarein reduces inflammatory responses by inhibiting Src kinase activity. Korean J. Physiol. Pharmacol. 19(5), 441-449 (2015).

    6. Shi, X., Chen, G., Liu, X., et alScutellarein inhibits cancer cell metastasis in vitro and attenuates the development of fibrosarcoma in vivo. Int. J. Mol. Med. 35(1), 31-38 (2015).