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Eliglustat

    
10mM in DMSO

Eliglustat

源叶(MedMol)
S54914 一键复制产品信息
491833-29-5
C23H36N2O4
404.54
依利格鲁司特;GENZ-112638;Octanamide;Genz 99067; N-[(1R,2R)-2-(2,3-Dihydro-1,4-benzodioxin-6-yl)-2-hydroxy-1-(1-pyrrolidinylmethyl)ethyl]-octanamide
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S54914-1ml促销
10mM in DMSO

¥296.00 ¥266.00

6 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: 葡萄糖神经酰胺合酶抑制剂;Glucosylceramide Synthase Inhibitors;;InformationEliglustat Eliglustat (GENZ-112638) inhibits glucosylceramide synthase(GCS) (IC50=20 nM in intact MDCK cells), thus reducing the load of glucosylceramide influx into the lysosome.Targetsglucosylceramide synthase (In intact MDCK cells) 20 nMIn vitroEliglustat tartrate is designed and developed to inhibit glucosylceramide synthase, the enzyme that catalyzes the formation of glucosylceramide from UDP-glucose and ceramide.The inhibition of glucosylceramide synthase by eliglustat tartrate is highly specific. Eliglustat tartrate displays limited or no activity against a variety of glycosidases. Additionally, no inhibition of sucrase or maltase is observed at drug concentrations up to 10 μM.In vivoPreclinical studies in normal mice, rats and dogs with i.v. and oral administration demonstrates significant dose-related decreases in spleen, kidney and liver glucosylceramide content, consistent with prior observations with the palmitoyl homologue.In rodents, Genz-112638 is rapidly metabolized with a half-life of 15–45 minutes.
靶点: IC50: 24 nM (glucocerebroside synthase)
体内研究: 与年龄匹配的对照动物相比,在底物显著积累之前接受药物处理的小鼠 (10 周龄) 表现出脾脏、肺和肝脏中葡萄糖神经酰胺水平和戈谢细胞数量减少。
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.472 ml 12.36 ml 24.719 ml
5 mM 0.494 ml 2.472 ml 4.944 ml
10 mM 0.247 ml 1.236 ml 2.472 ml
50 mM 0.049 ml 0.247 ml 0.494 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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