SZL P1-41 is Skp2 inhibitor, selectively suppresses Skp2 E3 ligase activity, but not activity of other SCF complexes.
规格 | 价格 | 会员价 | 库存 | 数量 | |||
---|---|---|---|---|---|---|---|
{[ item.pr_size ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_am, item.pr_size) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_am, item.pr_size) ]} |
{[ getRatePrice(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_am, item.pr_size) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate) ]} | 现货 | 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解
描述 | SZL P1-41, a specific inhibitor of Skp2, attaches to the F-box domain of Skp2, inhibiting the association with Skp1 and the formation of the Skp2 SCF complex. Similar to the effects of Skp2 deficiency, SZL P1-41 enhances apoptosis/senescence mediated by p27 and disrupts glycolysis driven by Akt. It exhibits anti-tumor activities. At concentrations ranging from 5 to 20μM over a period of 24 hours, it leads to the induction of endogenous p27 protein expression in PC3 cells. Additionally, it prompts the expression of p21, another substrate of Skp2.[1]. |
Animal study | Administered intraperitoneally, SZL P1-41 demonstrates a significant inhibitory effect on the growth of prostate and lung tumors in Nude mice implanted with A549 and PC3 tumor xenografts, at dosages between 40 and 80 mg/kg[1]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.38mL 0.48mL 0.24mL |
11.89mL 2.38mL 1.19mL |
23.78mL 4.76mL 2.38mL |
CAS号 | 222716-34-9 |
分子式 | C24H24N2O3S |
分子量 | 420.524 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,Room Temperature |
溶解度 |
DMSO: 2 mg/mL(4.76 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |