Ibiglustat
CAS No. 1401090-53-6
Ibiglustat ( Venglustat | Genz-682452 | GZ452 )
产品货号. M11673 CAS No. 1401090-53-6
一种口服活性、选择性和有效的葡萄糖神经酰胺合酶 (GCS) 抑制剂,可进入中枢神经系统 (CNS)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1017 | 有现货 |
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| 10MG | ¥1549 | 有现货 |
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| 25MG | ¥2539 | 有现货 |
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| 50MG | ¥3636 | 有现货 |
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| 100MG | ¥4797 | 有现货 |
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| 200MG | ¥6471 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥889 | 有现货 |
|
生物学信息
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产品名称Ibiglustat
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种口服活性、选择性和有效的葡萄糖神经酰胺合酶 (GCS) 抑制剂,可进入中枢神经系统 (CNS)。
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产品描述An orally active, selective and potent Glucosylceramide synthase (GCS) inhibitor with central nervous system (CNS) access; exhibits significantly lower tissue levels of GL-3 and lyso-GL-3 and a delayed progression of a thermal nociceptive response in administered Fabry mice; shows favorable pharmacological properties and safety profile.Other Indication Phase 2 Clinical(In Vitro):Ibiglustat (SAR402671) (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 can prevent additional GL-3 accumulation and could serve to ameliorate the abundant levels of this sphingolipid in FD cardiomyocytes.
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体外实验——
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体内实验——
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同义词Venglustat | Genz-682452 | GZ452
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通路Others
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靶点Other Targets
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受体glucosylceramide synthase
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研究领域Other Indications
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适应症Other Disease
化学信息
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CAS Number1401090-53-6
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分子量389.49
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分子式C20H24FN3O2S
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纯度>98% (HPLC)
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溶解度DMSO: 10 mM ( < 1 mg/ml refers to the product slightly soluble or insoluble )
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SMILESO=C(O[C@@H]1CN2CCC1CC2)NC(C)(C3=CSC(C4=CC=C(F)C=C4)=N3)C
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化学全称(3S)-1-azabicyclo[2.2.2]octan-3-yl N-{2-[2-(4-fluorophenyl)- 1,3-thiazol-4-yl]propan-2-yl}carbamate
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Ashe KM, et al. Mol Med. 2015 Apr 30;21:389-99.
2. Marshall J, et al. Mol Ther. 2016 Jun;24(6):1019-1029.
产品手册
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