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- 详细信息
- 技术资料
- 保存条件:
4°C, sealed storage, away from moisture
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1433286-70-4
- 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: | ¥1570.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥533.0 |
| 规格: | 5 mg | 产品价格: | ¥1150.0 |
| 规格: | 10 mg | 产品价格: | ¥1850.0 |
| 规格: | 25 mg | 产品价格: | ¥3900.0 |
| 规格: | 50 mg | 产品价格: | ¥5450.0 |
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666-15
CAS No. : 1433286-70-4
MCE 国际站:666-15
产品活性:666-15 是一种有效的选择性 CREB 抑制剂,IC50 为 81 nM。666-15 抑制乳腺癌异种移植模型中的肿瘤生长。
研究领域:Epigenetics
作用靶点:Epigenetic Reader Domain
In Vitro: 666-15 (73 nM; for 12 hours) significantly blocks the effects caused by MSN overexpression, including cell proliferation, invasion, soft agar colony formation ability, and the expression of CREB downstream genes. 666-15 inhibits MSN overexpression-induced CREB phosphorylation.
666-15 (1μM; pretreated 2 hour) effectively inhibits PE-induced CREB phosphorylation. 666-15 significantly decreases the protein expression of ANP and β-MHC and inhibits the activation of ER stress, including the expression of GRP78, CHOP, ATF6, and the phosphorylation of IRE1 in PE + siRNA + 666-15 group and PE + si-CTRP3 + 666-15 group.
666-15 potently inhibits cancer cell growth. In MDA-MB-231 and MDA-MB-468 cells, the GI50 for 666-15 is 73 and 46 nM, respectively. In A549 and MCF-7 cells, it exhibits robust activity as well with GI50 of 0.47 and 0.31 μM. 666-15 is also found to be a rather weak inhibitor of CREB-CBP interaction with IC50 of 18.27 μM. 666-15 inhibits CREB’s transcription activity in living cells independent of direct CREB or CBP binding interaction. 666-15 is very potent in inhibiting CREB’s transcription activity. 666-15 also inhibits endogenous CREB target gene expression, the transcript level of nuclear receptor related 1 protein (Nurr1/NR4A2).
In Vivo: 666-15 (10 mg/kg; IP; once a week; for 11 weeks) alone can play a good role in inhibiting the growth of breast cancer, and the combination with RP-56976 (DOC) shows a better effect.
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