store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
2-(Chloromethyl)-4-(4-nitrophenyl)thiazole 是一种从黄芪 (Astragalus propinquus) 中提取得到的天然产物。2-(Chloromethyl)-4-(4-nitrophenyl)thiazole 具有抗癌活性,通过抑制肿瘤相关巨噬细胞 (TAM) 的 M2 极化在肝细胞癌 (HCC) 中显示除抗肿瘤活性。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
10 mg | ¥ 423 | 现货 | ||
25 mg | ¥ 684 | 现货 | ||
50 mg | ¥ 988 | 现货 | ||
100 mg | ¥ 1,528 | 现货 | ||
500 mg | ¥ 4,272 | 待询 |
产品描述 | 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole is a natural product derived from Astragalus propinquus.2-(Chloromethyl)-4-(4-nitrophenyl)thiazole exhibits anticancer activity. 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole possesses anticancer activity and has been shown to be active in hepatocellular carcinoma (HCC) by inhibiting the M2 polarization of tumor-associated macrophages (TAM). |
体外活性 | Astragalus polysacharin (APS) (100 μg/mL; PBMCs) induced mature DCs could stimulate the proliferation of allogeneic T lymphocytes. The proliferation index of T cells increased with an increased ratio of stimulator cells to effector cells (P < 0.05). Levels of IL-12 and IFN-gamma in the co-culture supernatant significantly increased in a time-dependent manner (P < 0.05). APS could in vitro induce DCs to mature, promote its antigen-presenting capacity, effectively activate CTLs, and enhance the anti-tumor function of the organism.[2] |
体内活性 | Astragalus polysacharin (APS) (20 mg/kg; intragastric; once daily; 10 weeks; diabetes-induced SD rats) administration decreased the rats' fasting plasma glucose (FPG) levels and body weight. APS (20 mg/kg) administration improved the cognitive performance of diabetes-induced rats in the Morris water maze test. APS (20 mg/kg) administration reduced the number of dead cells in the CA1 region of the hippocampus. Furthermore, APS (20 mg/kg) administration obviously upregulated the phosphorylation levels CREB, NMDA, and CaMK II. CONCLUSIONS These results suggest that APS has neuroprotective effects, and it may be a candidate for the treatment of neurodegenerative diseases such as diabetic cognitive impairment.[1] |
别名 | 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole, 黄芪多糖, 89250-26-0 |
分子量 | N/A |
store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 31.25 mg/mL, Sonication is recommended.
DMSO: 50 mg/mL (196.32 mM)
对于不同动物的给药剂量换算,您也可以参考 更多...
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: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (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:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
Astragalus Polysacharin Tyrosine Kinase/Adaptors TAM Receptor 2-(Chloromethyl)-4-(4-nitrophenyl)thiazole 黄芪多糖 89250-26-0 Inhibitor inhibitor inhibit