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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
DKGI-I; Diacylglycerol kinase inhibitor I
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
93076-89-2
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥3134.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥1127.0 |
| 规格: | 5 mg | 产品价格: | ¥3100.0 |
| 规格: | 10 mg | 产品价格: | ¥4900.0 |
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R 59-022
CAS No. : 93076-89-2
MCE 国际站:R 59-022
产品活性:R 59-022 (DKGI-I) 是一种 DGK 抑制剂 (IC50: 2.8 µM)。R 59-022 抑制 OAG 磷酸化为 OAPA。R 59-022 是一种 5-HT Receptor 拮抗剂,可激活蛋白激酶 C (PKC)。R 59-022 增强血小板中凝血酶诱导的甘油二酯的产生,并抑制嗜中性粒细胞中磷脂酸的产生。
研究领域:Epigenetics | TGF-beta/Smad | GPCR/G Protein | Neuronal Signaling
作用靶点:PKC | 5-HT Receptor
In Vitro: R 59-022 (10 μM, 1 min) potentiates platelet aggregation.
R 59-022 (30 uM, 0-60 min) increases release of Noradrenaline in chromaffin cells.
R 59-022 (40 uM, 30 min) activates PKC in HeLa and U87 cells.
R 59-022 (0-10 uM, 4 h) blocks EBOV entry into Vero cells.
In Vivo: R 59-022 (2 mg/kg, i.p., 12 days) significantly increases median survival in SCID mice implanted with U87 GBM cells.
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