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- 详细信息
- 技术资料
- 保存条件:
-20°C, sealed storage, away from moisture and light
- 英文名:
ACT-519276; OGT2378
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
441061-33-2
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥3819.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥1488.0 |
| 规格: | 5 mg | 产品价格: | ¥3725.0 |
| 规格: | 10 mg | 产品价格: | ¥5488.0 |
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Sinbaglustat
CAS No. : 441061-33-2
MCE 国际站:Sinbaglustat
产品活性:Sinbaglustat (OGT2378) 是葡萄糖神经酰胺合成酶 (GCS) 和非溶酶体葡萄糖神经酰胺酶 (GBA2) 的双重抑制剂。Sinbaglustat 是一种可透过血脑屏障的的口服N-烷基亚氨基糖。Sinbaglustat 可用于与溶酶体功能障碍相关的中枢神经退行性疾病的研究。
研究领域:Neuronal Signaling
作用靶点:Glucosylceramide Synthase (GCS)
In Vitro: Sinbaglustat (OGT2378; 20 μM) reduces the synthesis of glucosylceramide and ganglioside by 93% and >95% in MEB4 melanoma cells compared with untreated MEB4 cells, respectively, without either cytotoxic or antiproliferative effects.
GBA2 is an enzyme involved in the catabolism of glycosphingolipids (GSLs). Sinbaglustat is 50-fold more potent in inhibiting GBA2 than GCS.
In Vivo: Sinbaglustat (OGT2378; administered p.o., in the powdered chow, at a dose of 2500 mg/kg/day, corresponding to 35-40 mg of Sinbaglustat per mouse per day) is highly effective in impeding melanoma tumor growth in vivo. The effectiveness of p.o. Sinbaglustat in this murine model suggests that inhibition of glycosphingolipid synthesis is a promising approach to inhibit tumor progression.
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