A pan-PPAR agonist
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Bavachinin

Item No. 19376

Technical Information
Formal Name
(2S)-2,3-dihydro-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one
CAS Number
19879-30-2
Synonyms
  • 7-O-Methylbavachin
Molecular Formula
C21H22O4
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 50 mg/mLDMF:PBS (pH 7.2)(1:3): 0.25 mg/mLDMSO: 30 mg/mLEthanol: 20 mg/mL
λmax
219, 233, 273, 320 nm
SMILES
O=C1C[C@@H](C2=CC=C(O)C=C2)OC3=C1C=C(C/C=C(C)/C)C(OC)=C3
InChi Code
InChI=1S/C21H22O4/c1-13(2)4-5-15-10-17-18(23)11-20(14-6-8-16(22)9-7-14)25-21(17)12-19(15)24-3/h4,6-10,12,20,22H,5,11H2,1-3H3/t20-/m0/s1
InChi Key
VOCGSQHKPZSIKB-FQEVSTJZSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Bavachinin is a natural flavanone first isolated from seeds of P. corylifolia. It is a pan-PPAR agonist (EC50s = 4.0, 8.1, and 0.74 µM for PPARα, β/δ, and γ, respectively).1 Bavachinin has synergistic effects when combined with thiazolidinediones or fibrates. It lowers glucose and triacylglycerol levels in db/db mice without inducing weight gain or hepatotoxicity.1 Bavachinin also has actions that block allergic inflammation, angiogenesis, and Aβ42 aggregation in vitro.2,3,4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Feng, L., Luo, H., Xu, Z., et alBavachinin, as a novel natural pan-PPAR agonist, exhibits unique synergistic effects with synthetic PPAR-γ and PPAR-α agonists on carbohydrate and lipid metabolism in db/db and diet-induced obese mice. Diabetologia 59(6), 1276-1286 (2016).

    2. Chen, X., Yang, Y., and Zhang, Y. Isobavachalcone and bavachinin from Psoraleae Fructus modulate Aβ42 aggregation process through different mechanisms in vitro. FEBS Lett. 587(18), 29350-29355 (2013).

    3. Chen, X., Wen, T., Wei, J., et alTreatment of allergic inflammation and hyperresponsiveness by a simple compound, Bavachinin, isolated from Chinese herbs. Cell. Mol. Immunol. 10(6), 497-505 (2013).

    4. Nepal, M., Choi, H.J., Choi, B.-Y., et alAnti-angiogenic and anti-tumor activity of Bavachinin by targeting hypoxia-inducible factor-. Eur. J. Pharmacol. 691(1-3), 28-37 (2012).