Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Xanthohumol and xanthohumol D are potent inducers of quinone reductase, suggests that they could be used as chemoprevention agents.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | Inquiry | $ 249.00 | |
5 mg | Inquiry | Inquiry |
Description | Xanthohumol and xanthohumol D are potent inducers of quinone reductase, suggests that they could be used as chemoprevention agents. |
Targets&IC50 | QR2:110 μM (IC50) |
In vitro | Six metabolites were obtained as a result of transformation of xanthohumol (1) by selected fungal cultures. Their structures were established on the basis of their spectral data. One of them: 2'-(2'''-hydroxyisopropyl)-dihydrofurano-[4',5':3',4']-4',2-dihydroxy-6'-methoxy-α±,β-dihydrochalcone (6) has not been previously reported in the literature. The antioxidant properties of hops flavonoids and Xanthohumol Derivatives were investigated using the 2,2'-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging method. The effects of these compounds on proliferation of MCF-7, PC-3 and HT-29 human cancer cell lines were determined by the SRB assay. |
Source |
Molecular Weight | 370.4 |
Formula | C21H22O6 |
CAS No. | 274675-25-1 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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Xanthohumol D 274675-25-1 Others inhibitor inhibit