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- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1170.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥600.0 |
| 规格: | 5 mg | 产品价格: | ¥1200.0 |
| 规格: | 10 mg | 产品价格: | ¥1800.0 |
| 规格: | 25 mg | 产品价格: | ¥3700.0 |
| 规格: | 50 mg | 产品价格: | ¥5550.0 |
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PD173955
CAS No. : 260415-63-2
MCE 国际站:PD173955
产品活性:PD173955 是具有口服活性的 Src (IC50= 22 nM)、Yes、Abl、ATP 和 MAP 激酶抑制剂。PD173955 能有效地阻止有丝分裂进程,具有抗癌活性。
研究领域:Protein Tyrosine Kinase/RTK
In Vitro: PD173955 inhibits cell growth in MDA-MB-468 and MCF-7 breast cancer cells with IC50 values of 500 nM and 1 μM, respectively.
PD173955 (100 nM; 10 min) significantly inhibits the activity of src and yes kinases in MDA-MB-468 breast cancer cells.
PD173955 (5 μM; 24 h) can block the cells in the G2-M phase and has anti-mitotic activity in MDA-MB-468 breast cancer cells.
PD166326 (0.1-1000 nM; 42 h) can inhibit cell proliferation in R10(-) cells with IC50 0.2 nM, and can inhibit stem cell factor (SCF) -dependent proliferation in parental MO7e cells with IC50 12 nM.
In Vivo: PD166326 (50 mg/kg; Oral gavage; Twice daily) has anti-leukemia activity in CML mice.
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文献和实验三句话读懂一篇 CNS:「神药」二甲双胍又出抗癌奇招;抑郁症
5. Nature Communications:揭示二甲双胍助力抗肿瘤的分子机制2021 年 8 月 24 日,中国科学院分子细胞科学卓越创新中心欧阳波课题组在 Nature Communications 发表研究论文 PD-L1 degradation is regulated by electrostatic membrane association of its cytoplasmic domain。该研究发现酸性磷脂对细胞程序化死亡配体 1(PD-L1)胞质域(PD-L1-CD)的上膜起着重要调控作用
Signal Transduction Inhibitors in Cellular Function
) Mitogen-Activated Protein Kinase Pathways Inhibitors of MEK PD184352, PD098059, U0126, R009-22110 (17,20,21
《Science》中科大团队重磅发现:肿瘤免疫检查点疗法潜在新靶点 肿瘤诱导的免疫抑制是癌症逃避免疫监视和免疫攻击的主要原因。目前,免疫检查点疗法(ICT)在一些癌症的临床治疗中有很好的效果,其通过靶向细胞毒性T淋巴细胞相关抗原 4(CTLA-4)和程序性细胞死亡蛋白 1(PD-1)来逆转 T 细胞的免疫抑制。但是仍有大约 70% 的癌症患者对 ICT 不敏感,因此,寻找有效的 ICT 靶点是非常必要的。最新的研究表明,中枢神经系统可以调节癌症的发展和免疫系统的活动,其中主要途径是通过神经
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