2,2'-Dihydroxy chalcone

TargetMol
Product Code: TAR-TN7224
Supplier: TargetMol
CodeSizePrice
TAR-TN7224-1mg1mg£227.00
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TAR-TN7224-5mg5mg£416.00
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TAR-TN7224-10mg10mg£581.00
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TAR-TN7224-25mg25mg£863.00
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TAR-TN7224-50mg50mg£1,163.00
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TAR-TN7224-100mg100mg£1,540.00
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TAR-TN7224-500mg500mg£3,026.00
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Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20°C

Images

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Further Information

Bioactivity:
2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6?0.2 uM) and lysozyme (IC50=1.4?0.2 uM) release from rat neutrophils stimulated with fMLP/CB.2,2'-Dihydroxy chalcone has inhibitory activity against Escherichia coli, Shigella fowleri, Staphylococcus albicans and Staphylococcus aureus.
CAS:
15131-80-3
Formula:
C15H12O3
Molecular Weight:
240.25
Pathway:
Autophagy|Microbiology/Virology
Purity:
0.98
SMILES:
O=C(C=CC=1C=CC=CC1O)C=2C=CC=CC2O
Target:
Autophagy|Antibacterial

References

Park H, et al. Hydroxylated Chalcones as Aryl Hydrocarbon Receptor Agonists: Structure-Activity Effects. Toxicol Sci. 2021;180(1):148-159. Haddad AQ, et al. Antiproliferative mechanisms of the flavonoids 2,2'-dihydroxychalcone and fisetin in human prostate cancer cells. Nutr Cancer. 2010;62(5):668-68 Pruitt R, et al. Radiosensitization of cancer cells by hydroxychalcones. Bioorg Med Chem Lett. 2010;20(20):5997-6000. Goh K, et al. 2,2'-Dihydroxychalcone, a glutathione transferase inhibitor, sensitises human colon adenocarcinoma cells to chlorambucil and melphalan, but not to actinomycin D. Mol Med Rep. 2008;1(4):575-579.