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7-Hydroxyflavone

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纯度: 99.79%

货号 T7472Cas号 6665-86-7

别名 7-羟基黄酮, 7羟基黄酮

7-Hydroxyflavone 是一种黄酮类化合物,从M. indica 中分离得到,具有抗炎活性。它利用 ERK/Nrf2/HO-1 通路保护肾细胞,使其免受尼古丁诱导的细胞毒性。

7-Hydroxyflavone
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7-Hydroxyflavone

一键复制产品信息
Rating icon 很棒

纯度: 99.79%

货号 T7472 别名 7-羟基黄酮, 7羟基黄酮Cas号 6665-86-7

7-Hydroxyflavone 是一种黄酮类化合物,从M. indica 中分离得到,具有抗炎活性。它利用 ERK/Nrf2/HO-1 通路保护肾细胞,使其免受尼古丁诱导的细胞毒性。

规格价格库存数量
10 mg
¥ 119
现货
25 mg
¥ 167
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50 mg
¥ 226
现货
100 mg
¥ 314
现货
500 mg
¥ 727
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产品介绍


7-Hydroxyflavone AI Summary
7-Hydroxyflavone demonstrates a variety of bioactivities across multiple biological assays. It shows inhibitory activity against ALR2 (aldose reductase) with an IC50 value of 14650.0 nM in bovine lenses and against COX-2 catalyzed PGE-2 production in LPS induced RAW 264.7 cells with a 70.8% inhibition rate at 10 µM concentration. It binds to benzodiazepine receptors with a Ki value of 4200.0 nM and interacts with the androgen receptor with an IC50 value greater than 42657.95 nM. Additionally, it shows significant inhibitory activity against hamster liver mitochondrial monoamine oxidase (MAO) with an IC50 of 120.0 nM. 7-Hydroxyflavone also displays low affinity for adenosine A1 and A2A receptors, with pKi values of -0.48 and -0.43 µM, respectively. It effectively lowers systolic blood pressure in anesthetized spontaneously hypertensive rats and provides significant protection from gastric damage in rats. Moreover, it inhibits bovine thymus p56Lck-catalyzed phosphorylation and beef heart mitochondrial enzymes, including a 95.1% inhibition of ATPase activity at 0.42 mM concentration. The compound has shown antiplasmodial activity with an IC50 of 65500.0 nM against Plasmodium falciparum NF54 and also inhibits FabZ enzyme with an IC50 of 20000.0 nM. It demonstrates antioxidant activity by inhibiting toxin-induced lipid peroxidation and shows inhibitory effects on carbonic anhydrase isozymes. 7-Hydroxyflavone induces adipogenesis in mouse 3T3L1 cells and exhibits vasorelaxant properties in Wistar rat thoracic aortic rings. It also shows antagonist activity at the alpha1-adrenoceptor in rat anococcygeal muscle and antiviral activity against Marburg virus and SARS-CoV-2. 7-Hydroxyflavone inhibits human 17beta-HSD1 and 17beta-HSD2 enzymes, demonstrating potential effects in hormone regulation. Furthermore, it exhibits cytotoxicity against human cell lines and moderate inhibition against multiple CYP enzymes, suggesting broad pharmacological properties..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
7-Hydroxyflavone is a potent inhibitor of CYP1A1 with a Ki value of 0.015 μM and exhibits 6-fold greater selectivity for CYP1A1 over CYP1A2.with anti-inflammatory activity
别名7-羟基黄酮, 7羟基黄酮
化学信息
分子量238.24
分子式C15H10O3
CAS No.6665-86-7
SmilesOc1ccc2c(c1)oc(cc2=O)-c1ccccc1
密度1.340 g/cm3 at 20℃
颜色Gray
物理性状Solid
储存&溶解度
存储keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 47 mg/mL (197.28 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (8.39 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM4.1974 mL20.9872 mL41.9745 mL209.8724 mL
5 mM0.8395 mL4.1974 mL8.3949 mL41.9745 mL
10 mM0.4197 mL2.0987 mL4.1974 mL20.9872 mL
20 mM0.2099 mL1.0494 mL2.0987 mL10.4936 mL
50 mM0.0839 mL0.4197 mL0.8395 mL4.1974 mL
100 mM0.0420 mL0.2099 mL0.4197 mL2.0987 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

方案所需的各类助溶剂如: DMSOPEG300 / PEG400Tween 80SBE-β-CD玉米油 等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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