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Submit ReviewMiglustat hydrochloride is an orally active α-glucosidase I and II and ceramide-specific glycosyltransferase inhibitor. Rescues trafficking-deficient F508del-CFTR in human airway epithelial cells via inhibition of ER α-glucosidases I and II. Also has broad spectrum antiviral activity.
分子量 | 255.74 |
公式 | C10H21NO4.HCl |
储存 | Desiccate at -20°C |
CAS Number | 210110-90-0 |
PubChem ID | 657399 |
InChI Key | QPAFAUYWVZMWPR-ZSOUGHPYSA-N |
Smiles | CCCCN1C[C@H](O)[C@@H](O)[C@H](O)[C@H]1CO.Cl |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
water | 19.18 | 75 | |
DMSO | 19.18 | 75 |
以下数据基于产品分子量 255.74。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.75 mM | 5.21 mL | 26.07 mL | 52.14 mL |
3.75 mM | 1.04 mL | 5.21 mL | 10.43 mL |
7.5 mM | 0.52 mL | 2.61 mL | 5.21 mL |
37.5 mM | 0.1 mL | 0.52 mL | 1.04 mL |
参考文献是支持产品生物活性的出版物。
Platt et al (1994) N-Butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis. J.Biol.Chem. 269 8362 PMID: 8132559
Dwek et al (2002) Targeting glycosylation as a therapeutic approach. Nat.Rev.Drug Disc. 1 65 PMID: 12119611
Noel et al (2008) Parallel improvements of sodium and chloride transport defects by migl. (n-butyldeoxynojyrimicin) in cystic fibrosis epithelial cells. J.Pharmacol.Exp.Ther. 325 1016 PMID: 18309088
If you know of a relevant reference for Miglustat hydrochloride, please let us know.
关键词: Miglustat hydrochloride, Miglustat hydrochloride supplier, α-glucosidase, alpha-glucosidase, I, II, inhibits, inhibitors, ceramide-specific, glycosyltransferases, Glycosylases, Carbohydrate, Metabolism, NBDNJ, N-Butyldeoxynojirimycin, hydrochloride, NB-DNJ, Other, Transferases, Non-selective, Antivirals, 3117, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 Miglustat hydrochloride 的部分引用包括:
Huang et al (2011) Glucosylceramide synthase inhibitor PDMP sensitizes chronic myeloid leukemia T315I mutant to Bcr-Abl inhibitor and cooperatively induces glycogen synthase kinase-3-regulated apoptosis. FASEB J 25 3661 PMID: 21705667
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