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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
- 保质期:
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
- 英文名:
PD 0325901; PD325901; PD-0325901
- 库存:
现货
- 供应商:
爱必信(上海)生物科技有限公司
- CAS号:
391210-10-9
- 规格:
100mg/50mg/10mg/5mg
| 规格: | 100mg | 产品价格: | ¥3740.0 |
|---|---|---|---|
| 规格: | 50mg | 产品价格: | ¥2421.0 |
| 规格: | 10mg | 产品价格: | ¥813.0 |
| 规格: | 5mg | 产品价格: | ¥459.0 |
| 公告提醒:爱必信所有产品和服务仅用于科学研究,不用于临床应用及其他用途提供产品和服务(也不为任何个人提供产品和服务)!
抑制剂描述: 产品名称:PD0325901 产品别名:见爱必信官网 英文别名:PD0325901 靶点:MEK CAS:391210-10-9 纯度:>98% 外观:见爱必信官网 保存方法:Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution. 描述: PD0325901 is a selective and non ATP-competitive MEK inhibitor with IC50 of 0.33 nM in cell-free assays, roughly 500-fold more potent than CI-1040 on phosphorylation of ERK1 and ERK2. Phase 2. 溶解性:DMSO : ≥ 56 mg/mL (116.14 mM) 体外研究: PF0325901 shows higher permeability, and should be able to achieve higher systemic exposures than CI-1040. PD0325901 is exquisitely specific and highly potent against purified MEK, revealing a Kiapp of 1 nM against activated MEK1 and MEK2. PD0325901 is roughly 500-fold more potent than CI-1040 with respect to its cellular effects on phosphorylation of ERK1 and ERK2, displaying subnanomolar activity. PD0325901 prevents the growth of melanoma cell lines. PD0325901 inhibits the growth of TPC-1 cells and K2 cells with GC50 of 11 nM and 6.3 nM, respectively. PD0325901 significantly prevents the the growth of PTC cells harboring a BRAF mutation at very low concentration (10 nM) and only moderately increases the growth of the PTC cells carrying the RET/PTC1 rearrangement at the same concentration. PD0325901 effectively inhibits the phosphorylation of ERK1/2 in multiple PTC cell lines. 体内研究:PD0325901 (25 mg/kg, p.o.) inhibits phosphorylation of ERK by more than 50% at 24 hours post-dosing. The dose required to produce a 70% incidence of complete tumor responses (C26 model) is 25 mg/kg/day versus 900 mg/kg/day for PD0325901 and CI-1040, respectively. Anticancer activity of PD 0325901 has been demonstrated for a broad spectrum of human tumor xenografts. PD0325901 (20-25 mg/kg/day, p.o.) treatment in mice, shows no tumor growth inoculated with PTC cells bearing a BRAF mutation. For PTC with the RET/PTC1 rearrangement, the average tumor volume of the orthotopic tumor is decreased by 58% as compared with controls. PTC cells carrying a BRAF mutation are more sensitive to PD0325901 than are PTC cells carrying the RET/PTC1 rearrangement.
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文献和实验A New Chemical Approach to the Efficient Generation of Mouse Embryonic Stem Cells
Here, we present a highly efficient and reproducible method for the establishment of mouse embryonic stem cells (mESCs) from embryonic day 3.5 (E3.5) whole blastocysts. This protocol involves the use of small molecules SB431542 and PD0325901
在了可生成结缔组织的成纤维细胞生成的自然过程研究上。这种自然发生过程称为MET(间质—上皮细胞转化),会使成纤维细胞更接近于干细胞样状态。研究小组测试了大量类药分子,寻找抑制TGFb(转化生长因子β)和MEK(裂原活化蛋白激酶)的路径。TGFb和MEK都参与MET过程。经过研究,他们发现两种化学物质——ALK5抑制剂SB43142和MEK抑制剂PD0325901——的组合,在促进成纤维细胞转化成干细胞方面的效用最高,比传统方法的效率高100倍。随后,研究人员又锁定了一种名为Thiazovivin的新型
「神药」再显威!杨黄浩等让二甲双胍扮演 PD-L1 「单抗」角色,提高治疗效果
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