A flavonoid with diverse biological activities
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Baicalein

Item No. 70610

Technical Information
Formal Name
5,6,7-trihydroxy-2-phenyl-4H-1-benzopyran-4-one
CAS Number
491-67-8
Molecular Formula
C15H10O5
Formula Weight
Purity
≥95%
A crystalline solid
DMF: 52 mg/mlDMSO: 28 mg/mlEthanol: 1.3 mg/mlPBS (7.2): <90 µg/ml
λmax
216, 277, 324 nm
SMILES
OC1=CC2=C(C(C=C(C3=CC=CC=C3)O2)=O)C(O)=C1O
InChi Code
InChI=1S/C15H10O5/c16-9-6-11(8-4-2-1-3-5-8)20-12-7-10(17)14(18)15(19)13(9)12/h1-7,17-19H
InChi Key
FXNFHKRTJBSTCS-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Baicalein is a flavonoid originally isolated from the roots of S. baicalensis that has diverse biological activities.1 It inhibits human platelet 12-lipoxygenase (12-LO) and human reticulocyte 15-LO-1 (IC50s = 0.64 and 1.6 µM, respectively) but is less potent at 15-LO-1 when the detergent Triton-X is present (IC50 = 38 µM).2 Baicalein inhibits lipid peroxidation, as assessed by production of thiobarbituric acid (TBARS; IC50 = 5 µM), and inhibits growth of Huh-7, KIM-1, and HLF human hepatocellular carcinoma cells (IC50s = 17-70 µg/ml).3,4 Baicalein increases intracellular calcium levels by increasing release from the endoplasmic reticulum and via PKC-dependent calcium channels in the plasma membrane, leading to increases in reactive oxygen species (ROS), caspase-9 and -3 activation, and apoptosis in ZR-75-1 human breast cancer cells.5 Baicalein increases levels of peroxisome proliferator-activated receptor β/δ (PPARβ/δ) in BV-2 microglia and primary microglia and decreases the level of 12- and 15-LO products.6 It also decreases symptoms of experimental autoimmune encephalomyelitis (EAE) in a mouse model of multiple sclerosis, when administered at a dose of 75 mg/kg per day.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Shibata, K., Iwata, S., and Nakamura, M. Baicalin, a new flavone-glucuronic acid compound from the roots of Scutellaria baicalensis. Acta Phytochimica 1, 105-139 (1923).

    2. Deschamps, J.D., Kenyon, V.A., and Holman, T.R. Baicalein is a potent in vitro inhibitor against both reticulocyte 15-human and platelet 12-human lipoxygenases. Bioorg. Med. Chem. 14(12), 4295-4301 (2006).

    3. Matsuzaki, Y., Korokawa, N., Terai, S., et alCell death induced by baicalein in human hepatocellular carcinoma cell lines. Jpn. J. Cancer Res. 87(2), 170-177 (1996).

    4. Gao, D., Sakurai, K., Katoh, M., et alInhibition of microsomal lipid peroxidation by baicalein: A possible formation of an iron-baicalein complex. Biochem. Mol. Biol. Int. 39(2), 215-225 (1996).

    5. Chang, H.-T., Chou, C.-F., Kuo, D.-H., et alThe mechanism of Ca2+ movement in the involvement of baicalein-induced cytotoxicity in ZR-75-1 human breast cancer cells. J. Nat. Prod. 78(7), 1624-1634 (2015).

    6. Xu, J., Zhang, Y., Xiao, Y., et alInhibition of 12/15-lipoxygenase by baicalein induces microglia PPARβ/δ: A potential therapeutic role for CNS autoimmune disease. Cell Death Dis. 4(4), e569 (2013).