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Bavachalcone

Cat. No. M13460

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Bavachalcone Structure
Synonym:

Broussochalcone B

Size Price Availability Quantity
1mg USD 60  USD60 In stock
5mg USD 135  USD135 In stock
10mg USD 195  USD195 In stock
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Quality Control & Documentation
Biological Activity

Bavachalcone is a major bioactive compounds isolated from Psoralea corylifolia L.; has been widely used as traditional Chinese medicine; antibiotic or anticancer agent. IC50 value: Target: Bavachalcone inhibited osteoclast formation from precursor cells with the IC(50) of approximately 1.5 microg ml(-1). The activation of MEK, ERK, and Akt by receptor activator of nuclear factor kappaB ligand (RANKL), the osteoclast differentiation factor, was prominently reduced in the presence of bavachalcone. The induction of c-Fos and NFATc1, key transcription factors for osteoclastogenesis, by RANKL was also suppressed by bavachalcone. Bavachalcone exhibited a significant inhibitory effect on baculovirus-expressed BACE-1 in vitro. Bavachalcone had stronger inhibition on UGT1A1 and UGT1A7 than corylin which did not inhibit UGT1A1, UGT1A3, UGT1A7, UGT1A8, UGT1A10, and UGT2B4. Data fitting using Dixon and Lineweaver-Burk plots demonstrated the noncompetitive inhibition of bavachalcone against UGT1A1 and UGT1A7-mediated 4-MU glucuronidation reaction. The values of inhibition kinetic parameters (Ki) were 5.41 μ M and 4.51μ M for UGT1A1 and UGT1A7, respectively.

Chemical Information
Molecular Weight 324.37
CAS Number 28448-85-3
Solubility (25°C) DMSO ≥ 34 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Hae Seong Song, et al. Phytomedicine. Bavachalcone from Cullen corylifolium induces apoptosis and autophagy in HepG2 cells

[2] Dan Zhou, et al. Biomed Chromatogr. Quantitative bioanalysis of bavachalcone in rat plasma by LC-MS/MS and its application in a pharmacokinetics study

[3] Yanqi Dang, et al. Pharmacology. Bavachalcone-induced manganese superoxide dismutase expression through the AMP-activated protein kinase pathway in human endothelial cells

[4] Lina Shan, et al. Evid Based Complement Alternat Med. Comparison of the Inhibitory Potential of Bavachalcone and Corylin against UDP-Glucuronosyltransferases

[5] Cheol Kyu Park, et al. Biochem Pharmacol. Bavachalcone inhibits osteoclast differentiation through suppression of NFATc1 induction by RANKL

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Keywords: Bavachalcone, Broussochalcone B supplier, Antibiotic, inhibitors, activators

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