Catalog No. A3664
Nordihydroguaiaretic acid
(别名:去甲二氢愈创木酸)
抗肿瘤剂;脂氧合酶抑制剂
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 100mg | ¥436.00 | 现货 | |
| 500mg | ¥890.00 | 现货 |
CAS号:500-38-9纯度:99.83%
仅用于科研,不用于诊疗。未经明确授权不得转售。
A
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特色产品
Phos binding reagent (Phosbind) acrylamide
分离和检测磷酸化/非磷酸化蛋白
- 新型的磷酸盐结合标签和功能分子
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
Cy5 TSA Fluorescence System Kit
Cy5荧光标记的酪胺信号放大系统
- 检测ICC/IHC/ISH中的低丰度靶点
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
EZ Cap™ Cy5 Firefly Luciferase mRNA (5-moUTP)
用于观察mRNA运送,定位,翻译
- 具有Cap1结构的荧光素酶mRNA
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
Description:IC50 Value: N/ANordihydroguaiaretic acid (NDGA) is a natural phenolic compound isolated from the creosote bush Larrea divaricata, which has anti-tumor activities both in vitro and in vivo. Its analogs are in clinical development for use in refractory solid tumors.in vitro: NDGA may also direct target mTORC1 complex because NDGA suppressed amino acids- and insulin-stimulated mTORC1 and acted like rapamycin to disrupt mTOR-Raptor interaction [1]. NDGA increased PPARα promoter activity in AML12 hepatocytes and also prevented the fatty acid suppression of PPARα expression. In contrast, PPARα siRNA abrogated the stimulatory effect of NDGA on fatty acidcatabolism [2].in vivo: NDGA was able to induce Nrf2 translocation in vivo in kidneys of rats submitted to both U-NX and I/R injury and to protect against renal histological damage and apoptosis [3]. Comparison of the proportion of live mice at the age of 90% mortality was used as a surrogate for measurement of maximum lifespan;neither NDGA (p=0.12) nor aspirin (p=0.16) had a significant effect in this test. Measures of blood levels of NDGA or aspirin and its salicylicacid metabolite suggest that the observed lack of effects of NDGA or aspirin on life span in females could be related to gender differences in drug disposition or metabolism [4].Clinical trial: Nordihydroguaiaretic Acid in Treating Patients With Nonmetastatic Relapsed Prostate Cancer . Phase 1
产品性质
| 物理外观 | A solid |
| CAS号 | 500-38-9 |
| 分子式 | C18H22O4 |
| 分子量 | 302.36 |
| 化学名称 | 4,4'-(2,3-dimethylbutane-1,4-diyl)bis(benzene-1,2-diol) |
| 溶解度 | insoluble in H2O; ≥107 mg/mL in EtOH; ≥121 mg/mL in DMSO |
| SMILES | CC(Cc(cc1)cc(O)c1O)C(C)Cc(cc1)cc(O)c1O |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | 去甲二氢愈创木酸是一种 5-脂氧合酶(5LOX)抑制剂,其 IC50 值为 8 μM,同时也是一种酪氨酸激酶抑制剂。 |
质量控制
APExBIO 顾客使用本产品发表的 1 篇科研文献
摩尔浓度计算器
质量
= 浓度
x 体积
x 分子量
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Apexbio的产品页面获得)批次特异的分子量使用本工具。



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