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Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
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货期:1-2天
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| 规格: | 1 mg | 产品价格: | ¥271.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥684.0 |
| 规格: | 10 mg | 产品价格: | ¥1118.0 |
| 规格: | 25 mg | 产品价格: | ¥1888.0 |
| 规格: | 50 mg | 产品价格: | ¥2788.0 |
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PD180970
CAS No. : 287204-45-9
MCE 国际站:PD180970
产品活性:PD180970 是一种高效且具有 ATP 竞争性的 p210Bcr-Abl 激酶抑制剂,可抑制 p210Bcr-Abl 的自磷酸化,IC50 为 5 nM。PD180970 还抑制 Src 和 KIT 激酶,IC50 分别为 0.8 nM 和 50 nM。PD180970 可诱导 K562 白血病细胞凋亡 (apoptosis),可用于慢性粒细胞白血病的研究。
研究领域:Protein Tyrosine Kinase/RTK | Apoptosis
作用靶点:Bcr-Abl | Src | c-Kit | Apoptosis
In Vitro: PD180970 (0.5 μM; 24-96 hours) treatment causes cell death K562 cells.
PD180970 (0.5 μM; 24-48 hours) treatment induces apoptosis of K562 cells. The result shows increase in annexin V-PI double-positive cells.
PD180970 inhibits tyrosine phosphorylation of p210Bcr-Abl, Gab2, and CrkL in K562 cells with IC50 values of 170 nM, 80 nM, and 80 nM, respectively. In vitro, PD180970 potently inhibits autophosphorylation of p210Bcr-Abl (IC50 of 5 nM) and the kinase activity of purified recombinant Abl tyrosine kinase (IC50 of 2.2 nM).
The blocking Bcr-Abl kinase activity using PD180970 in the human K562 CML cell line resulted in inhibition of Stat5 DNA-binding activity with an IC50 of 5 nM.
In Vivo: PD180970 (5 mg/kg; intraperitonial injection; daily; for 7 days) mitigates MPTP-induced neuronal loss in mice. PD180970 has the neuroprotective ability in a preclinical mouse model of Parkinson's disease (PD).
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