柯因二甲醚 T5778
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
50 mg | 21392-57-4 | ¥913.00 | 询底价 |
10 mg | 21392-57-4 | ¥289.00 | 询底价 |
100 mg | 21392-57-4 | ¥1,350.00 | 询底价 |
25 mg | 21392-57-4 | ¥578.00 | 询底价 |
1 mL | 21392-57-4 | ¥260.00 | 询底价 |
500 mg | 21392-57-4 | ¥3,390.00 | 询底价 |
5 mg | 21392-57-4 | ¥198.00 | 询底价 |
Product Introduction
Bioactivity
英文名: 5,7-DIMETHOXYFLAVONE
描述: 5,7-Dimethoxyflavone 是一种 Kaempferia parviflora 的主要成分,具有抗肿瘤、抗肥胖及抗炎活性。它对细胞色素 P450 (CYP) 3As 具有抑制作用,也是抗乳腺癌蛋白 (BCRP) 抑制剂。
体外活性: The best in vitro trypanocidal activity for T. brucei rhodesiense was exerted by 7,8-dihydroxyflavone (50% inhibitory concentration [IC50], 68 ng/ml), followed by 3-hydroxyflavone, rhamnetin, and 7,8,3',4'-tetrahydroxyflavone (IC50s, 0.5 microg/ml) and catechol (IC50, 0.8 microg/ml).?The activity against T. cruzi was moderate, and only Chrysin dimethylether and 3-hydroxydaidzein had IC50s less than 5.0 microg/ml.
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 50 mg/mL (177.12 mM)
关键字: anti-inflammatory | Cytochrome P450 | Anti-obesity | CYPs | 5,7 DIMETHOXYFLAVONE | inhibit | CYP3As | antineoplastic | BCRP | 5,7-DIMETHOXYFLAVONE | 5,7-Dimethoxyflavone | Inhibitor | 5,7DIMETHOXYFLAVONE
相关产品: 7-Hydroxyflavanone | Pyrolin | Isoschaftoside | 8-Epidiosbulbin E acetate | 4-Acetamidobenzenesulfonamide | 2'-Hydroxy-4'-methylacetophenone | Octahydrocurcumin | Quercimeritrin | Nevadensin | Sulfabrom
相关库: Selected Plant-Sourced Compound Library | Bioactive Compounds Library Max | Inhibitor Library | Traditional Chinese Medicine Monomer Library | Anti-Cancer Active Compound Library | Natural Product Library for HTS | Metabolism Compound Library | Flavonoid Natural Product Library | NO PAINS Compound Library | Natural Product Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途