Ibiglustat succinate Venglustat succinate; SAR402671 succinate; GZ402671 succinate,99.92%
产品编号:Bellancom-16743B| CAS NO:1629063-80-4| 分子式:C24H30FN3O6S| 分子量:507.57
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Ibiglustat succinate Venglustat succinate; SAR402671 succinate; GZ402671 succinate
产品介绍 | Ibiglustat (Venglustat) succinate是一种具有口服活性的,可透过血脑屏障地葡糖神经酰胺合酶 (GCS) 抑制剂。Ibiglustat succinate 可用于研究戈谢病 3 型、与 GBA 突变相关的帕金森病、法布瑞氏症、GM2 神经节苷脂病和常染色体显性多囊肾病。 | ||||||||||||||||
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生物活性 | Ibiglustat (Venglustat) succinate is an orally active, brain-penetrant glucosylceramide synthase (GCS) inhibitor. Ibiglustat succinate can be used for the research of Gaucher disease type 3, Parkinson's disease associated with GBA mutations, Fabry disease, GM2 gangliosidosis, and autosomal dominant polycystic kidney disease. | ||||||||||||||||
体外研究 |
Ibiglustat (SAR402671) succinate (1 μM, 15 days; Fabry disease (FD) cells) is close to the physiological level in untreated WT cells in GL-3 levels, suggesting that Ibiglustat succinate can prevent additional GL-3 accumulation and could serve to ameliorate the abundant levels of this sphingolipid in FD cardiomyocytes[4]. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 | |||||||||||||||||
体内研究 | |||||||||||||||||
性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : ≥ 250 mg/mL (492.54 mM) * "≥" means soluble, but saturation unknown. 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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参考文献 |
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