- 全部删除
- 您的购物车当前为空
Ran-IN-1 (Compound M36) 是一种选择性和口服活性的Ran GTPase抑制剂。Ran-IN-1 高度特异性地与GDP结合态的Ran (RanGDP)的switch II口袋非共价结合,使其保持失活状态,并减少活性Ran-GTP的生成。Ran-IN-1能够诱导上皮性卵巢癌 (EOC) 细胞的凋亡 (apoptosis),并抑制例如HR和NHEJ等DNA修复途径。Ran-IN-1 被认为在上皮性卵巢癌,特别是高级别浆液性癌的研究中具有潜力。
Ran-IN-1 (Compound M36) 是一种选择性和口服活性的Ran GTPase抑制剂。Ran-IN-1 高度特异性地与GDP结合态的Ran (RanGDP)的switch II口袋非共价结合,使其保持失活状态,并减少活性Ran-GTP的生成。Ran-IN-1能够诱导上皮性卵巢癌 (EOC) 细胞的凋亡 (apoptosis),并抑制例如HR和NHEJ等DNA修复途径。Ran-IN-1 被认为在上皮性卵巢癌,特别是高级别浆液性癌的研究中具有潜力。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 待询 | 10-14周 | |
50 mg | 待询 | 10-14周 |
产品描述 | Ran-IN-1 (Compound M36) is an orally active and selective inhibitor of Ran GTPase. It binds allosterically with high specificity to the switch II pocket of GDP-bound Ran (RanGDP), stabilizing its inactive state and reducing the formation of active Ran-GTP. Ran-IN-1 induces apoptosis in epithelial ovarian cancer (EOC) cells and inhibits DNA repair pathways such as homologous recombination (HR) and non-homologous end joining (NHEJ). This compound shows potential for research in epithelial ovarian cancer, particularly in high-grade serous carcinoma. |
分子量 | 517.56 |
分子式 | C27H26F3NO4S |
CAS No. | 2301869-11-2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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。
评论内容