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Xanthohumol 是从啤酒花中分离到的黄酮类化合物,可抑制 COX-1 和 COX-2 活性,具有抗肿瘤,抗血管生成的作用,还具有抗多种病毒的活性。
Xanthohumol 是从啤酒花中分离到的黄酮类化合物,可抑制 COX-1 和 COX-2 活性,具有抗肿瘤,抗血管生成的作用,还具有抗多种病毒的活性。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 248 | 现货 | |
5 mg | ¥ 578 | 现货 | |
10 mg | ¥ 913 | 现货 | |
25 mg | ¥ 1,830 | 现货 | |
50 mg | ¥ 2,720 | 现货 | |
100 mg | ¥ 3,970 | 现货 | |
500 mg | ¥ 8,460 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 638 | 现货 |
产品描述 | Xanthohumol, also known as 2', 4, 4'-trihydroxy-6'-methoxy-3'-prenylchalcone or desmethylxanthohumol, is a member of the class of compounds known as 3-prenylated chalcones. It inhibits COX-1 and COX-2 activity and shows chemopreventive effects. |
靶点活性 | DGAT-2:40 μM (IC50), DGAT-1:40 μM (IC50) |
体外活性 | Xanthohumol抑制小鼠肝癌细胞培养中的Cyp1A活性并诱导QR活性。Xanthohumol清除活性氧物种,抑制超氧阴离子自由基和一氧化氮的产生。此外,Xanthohumol通过抑制DNA合成、诱导细胞周期在S期停滞、凋亡及细胞分化来阻止癌症的发生。[1] Xanthohumol还显示出强大的抗HIV-1活性。[2] |
体内活性 | 在CETP-Tg小鼠中,黄腐酚(p.o.)阻止胆固醇积聚导致动脉粥样硬化。[3] 在TRAMP小鼠中,黄腐酚(p.o.)促成尿生殖道(UG)平均重量下降, 延缓高级肿瘤进展并抑制低分化前列腺癌的生长。[4] |
激酶实验 | Inhibition of Cox Activity: Inhibition of Cox-1 activity is measured by monitoring oxygen consumption during the conversion of arachidonic acid to PGs using a Clark-type O2-electrode. The reaction mixture contains ~0.2 units Cox-1 in 100 μL of microsome fraction derived from ram seminal vesicles as a crude source of Cox-1 (specific activity 0.2–1 units/mg protein) or 0.23 units of recombinant human Cox-2 (specific activity 43 units/mg protein). For calculation, the rate of O2 consumption is compared with a DMSO control (100% activity). Piroxicam, a nonsteroidal anti-inflammatory drug, is used as positive inhibitory substance for Cox-1 activity with an IC50 of 0.35 ± 0.05 μM (n = 2). Alternatively, nimesulide, a Cox-2 specific inhibitor, inhibits Cox-2 activity by 52 ± 5.7% (n = 2) at a concentration of 50 μM. |
细胞实验 | HL-60 cells are maintained in RPMI 1640 supplemented with 10% FBS at 37°C in a 5% CO2 atmosphere. Log-phase cells with a population doubling time of 14–16 h are used for experiments. Serial 2-fold dilutions of compounds (dissolved in DMSO, final concentration 0.1%) in a final concentration range of 0.2–12.5 μM are prepared in 24-well plates using 1 ml of RPMI/well. Control wells obtain the same amount of solvent. Subsequently, 1 ml of the cell suspension is added to the wells. After 96 h, the experiment is evaluated. Cell numbers are counted using a Casy 1 TTC flow-cytometer. The proliferation of treated cells is expressed as a percentage in comparison with the solvent control.(Only for Reference) |
别名 | 黄腐醇 |
分子量 | 354.4 |
分子式 | C21H22O5 |
CAS No. | 6754-58-1 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||||||||||||
溶解度信息 | Ethanol: 35.4 mg/mL (100 mM) DMSO: 5.63 mg/mL (15.87 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||||||||||||
DMSO/Ethanol
Ethanol
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