2,2'-Dihydroxy chalcone
產(chǎn)品名稱:2,2'-Dihydroxy chalcone
產(chǎn)品描述:
| 結(jié)構(gòu)類型 | 天然產(chǎn)物 > 酚類 |
| 產(chǎn)品描述 | 2,2'-Dihydroxy chalcone is a potent inhibitor of β-glucuronidase (IC50=1.6±0.2 μM) and lysozyme (IC50=1.4±0.2 μM) 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. |
| 體外活性 | 2,2'-dihydroxychalcone (DHC) (1-50 microM) caused a dose-dependent reduction in viability, a concomitant increase in apoptosis in PC3 cells at 72 h, and a decrease in clonogenic survival at 24 h treatment. DHC was considerably more potent than fisetin in these cytotoxicity assays. The mechanism of accelerated cellular senescence was not activated by DHC in PC3 or lymph node carcinoma of the prostate (LNCaP) cells.[1] |
| 分子量 | 240.25 |
| 分子式 | C15H12O3 |
| CAS No. | 15131-80-3 |
存儲
Powder: -20°C for 3 years | In solvent: -80°C for 2 years
溶解度
( < 1 mg/mL refers to the product slightly soluble or insoluble )
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