计算溶液所需的质量、体积或浓度。
| 活性类型 | 活性值-log(M) | 作用机制 | 期刊 | 参考文献(PubMed IDs) |
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Moligand™ 级 ,适用于对基线干扰要求严格的色谱和分析工作流程。
-80℃储存。特低温运输 。请查阅批次 COA 获取详细规格。
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在色谱分析、有机合成和交叉偶联反应领域已被 30 篇同行评审文献引用。
微溶于水,溶于丙酮、甲醇、乙醇(沸腾下)、碱和溶纤素,微溶于苯、四氯化碳、甲苯、二甲苯、吡啶、二硫化碳和冰乙酸,不溶于乙醇(冷)、斯淘特溶剂,溶于碱液呈蓝紫色,遇浓硫酸呈黄光红色,稀释后产生红光黄色沉淀,遇氢氧化钠为紫色。110℃升华(0.27kPa)。半数致死量(小鼠,腹腔)500mg/kg. 酸碱指示剂(0.5%溶液),pH变色范围5.5(黄色)-6.8(红色)。作铝、铟、汞、锌和锆的点滴试剂。神经组织和原生动物活体染色剂。
Information
Alizarin (Anthraquinonic) strongly inhibits P450 isoform CYP1A1, CYP1A2 andCYP1B1withIC50of 6.2 μM, 10.0 μM and 2.7 μM, respectively; weakly inhibits CYP2A6 and CYP2E1, and does not inhibit CYP2C19, CYP3A4 and CYP3A5.
In vitro
Alizarin weakly inhibits CYP2A6 and CYP2E1. Alizarin shows competitive inhibition against CYP1B1 with Ki of 0.5 μM. Alizarin reduces the mutagenicity of MeIQx, which induced by each CYP1A2 or CYP1B1, while does not effectively reduce the mutation induced by B[a]P. Alizarin exhibits antioxidants against iodophenol-derived phenoxyl radicals, superoxide anion radicals and lipid peroxidation in rat liver microsomes.
In vivo
Alizarin also reduces the hepatic content of thiobarbituric acid-reactive substances and the serum level of alanine aminotransferase in poisoned animals.
Cell Data
cell lines:
Concentrations:
Incubation Time:
Powder Purity:≥97%
H317: 可能引起皮肤过敏反应
H318: 造成严重的眼睛损伤
H410: 对水生生物有剧毒并具有长期持续影响