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Anticancer agent 73 是一种抗癌剂,它能有效地靶向反式激活反应(TAR)RNA 结合蛋白2(TRBP),并破坏TRBP-Dicer 的相互作用。Anticancer agent 73 通过调节 HCC 细胞中 miRNA 组和蛋白质组的表达谱,在体外和体内抑制 HCC 的生长和转移。


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Anticancer agent 73 是一种抗癌剂,它能有效地靶向反式激活反应(TAR)RNA 结合蛋白2(TRBP),并破坏TRBP-Dicer 的相互作用。Anticancer agent 73 通过调节 HCC 细胞中 miRNA 组和蛋白质组的表达谱,在体外和体内抑制 HCC 的生长和转移。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 2 mg | ¥ 127 | In stock | |
| 5 mg | ¥ 208 | In stock | |
| 10 mg | ¥ 348 | In stock | |
| 25 mg | ¥ 697 | In stock | |
| 50 mg | ¥ 1,030 | In stock | |
| 100 mg | ¥ 1,560 | In stock | |
| 200 mg | ¥ 2,190 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 230 | In stock |
Anticancer agent 73 相关产品
| 产品描述 | Anticancer agent 73 is an anticancer agent which potently targets transactivation response(TAR) RNA-binding protein 2 (TRBP) and disrupts the TRBP-Dicer interaction. Anticancer agent 73 suppresses the growth and metastasis of HCC in vitro and in vivo by modulating expression profiles of miRNAome and proteome in HCC cells. |
| 体外活性 | Anticancer agent 73(10 μM;6小时)在SK-HEP-1细胞中提高了E-cadherin的表达水平,并降低了纤维连接蛋白、N-cadherin和vimentin的蛋白质水平。此外,通过抑制miRNA的生物合成,它抑制了SK-HEP-1、HCCLM3和MHCC97L细胞的增殖和迁移。[1] |
| 体内活性 | Anticancer agent 73(10、25及50 mg/kg;静脉注射;每2天一次,持续4周;SCID小鼠)能有效降低SK-HEP-1细胞及在SCID小鼠体内植入的SK-HEP-1细胞的增殖和迁移。[1] |
| 别名 | 抗癌剂73 |
| 分子量 | 261.27 |
| 分子式 | C14H15NO4 |
| CAS No. | 124811-87-6 |
| Smiles | CCOC(=O)c1nc(oc1C)-c1ccc(OC)cc1 |
| 存储 | 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: 90.0 mg/mL (344.5 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
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