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- 详细信息
- 技术资料
- 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
- CAS号:
2252395-44-9
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1320.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥545.0 |
| 规格: | 5 mg | 产品价格: | ¥1200.0 |
| 规格: | 10 mg | 产品价格: | ¥1900.0 |
| 规格: | 50 mg | 产品价格: | ¥5500.0 |
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J22352
CAS No. : 2252395-44-9
MCE 国际站:J22352
产品活性:J22352 是一种具有类似靶向嵌合体蛋白水解 (PROTAC) 特性、高度选择性 HDAC6 抑制剂,其 IC50 值为 4.7 nM,J22352 通过抑制胶质母细胞瘤自噬、诱发抗肿瘤免疫反应来促进 HDAC6 降解和诱导抗癌效果,并通过降低 PD-L1 的免疫抑制活性,使宿主抗肿瘤活性恢复。
研究领域:Cell Cycle/DNA Damage | Epigenetics
作用靶点:HDAC
In Vitro: J22352 (0.1-20 μM; 72 hours) decreases U87MG cell viability in a dose-dependent manner.
?J22352 (10 μM; 24 hours) shows a dose-dependent decrease in HDAC6 protein abundance.
In Vivo: J22352 (10?mg/kg; given i.p. per day for 14 days in male nude mice) results in a >80% tumor growth inhibition (TGI) rate. J22352 is well tolerated in mice.
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