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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20°C, stored under nitrogen
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1936422-33-1
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥3700.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥1714.0 |
| 规格: | 5 mg | 产品价格: | ¥3200.0 |
| 规格: | 10 mg | 产品价格: | ¥5200.0 |
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GNE-781
CAS No. : 1936422-33-1
MCE 国际站:GNE-781
产品活性:GNE-781 是一种有效的,具有口服活性的选择性 CBP 抑制剂,在 TR-FRET 实验中 IC50 为 0.94 nM。GNE-781 还抑制 BRET 和 BRD4 (1),IC50 分别为 6.2 nM 和 5100 nM。GNE-781 在 MOLM-16 AML 异种移植模型中显示抗肿瘤活性。
研究领域:Epigenetics
作用靶点:Epigenetic Reader Domain | Histone Acetyltransferase
In Vitro: GNE-781 is a highly advanced potent and selective bromodomain inhibitor of cyclic adenosine monophosphate response element binding protein, binding protein (CBP). GNE-781 reduces FOXP3 (forkhead box P3) transcript levels. Examination of a subset of bromodomains reveals that GNE-781 is exquisitely selective for CBP/P300 and is remarkably selective for CBP (5425-fold) and P300 (4250-fold). GNE-781 demonstrates an appropriate balance of cell potency, selectivity (5425-fold over BRD4(1)) .
In Vivo: GNE-781 (3-30 mg/kg; p.o.; twice daily for 21 days) has tumor growth inhibition (%TGI) is 73%, 71%, and 89% at 3, 10, and 30 mg/kg, respectively in SCID beige mice with MOLM-16 AML xenografts.
?GNE-781 decreases Foxp3 transcript levels in a dose dependent manner. GNE-781 (3-30 mg/kg) suppresses MYC at doses as low as 3 mg/kg at 2 and 8 h, with maximal suppression at 10 and 30 mg/kg at 2 h (87% and 88% inhibition, respectively).
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