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N-(n-Butyl)deoxygalactonojirimycin Sale

(Synonyms: N-(正丁基)脱氧半乳糖霉素,NB-DGJ; N-(n-Butyl)deoxygalactonojirimycin) 目录号 : GC41235

An inhibitor of glucosylceramide synthase, glucocerebrosidase, and β-glucosidase 2

N-(n-Butyl)deoxygalactonojirimycin Chemical Structure

Cas No.:141206-42-0

规格 价格 库存 购买数量
500μg
¥619.00
现货
1mg
¥1,095.00
现货
5mg
¥2,712.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

N-(n-Butyl)deoxygalactonojirimycin is an inhibitor of α-D-galactosidase. It has also been shown to prevent glucosylceramide biosynthesis both in vitro and in mouse models of lysosome storage disorders by inhibiting the ceramide-specific glucosyltransferase, UDP-glucose ceramide glucosyltransferase (IC50 = 41.4 µM) without affecting α-glucosidase I and II or β-glucocerebrosidase (IC50s > 1 mM). This compound has been used to sensitize cultured chronic lymphocytic leukemia cells to the chemotherapeutic agents cladribine , chlorambucil , and fludarabine .

Chemical Properties

Cas No. 141206-42-0 SDF
别名 N-(正丁基)脱氧半乳糖霉素,NB-DGJ; N-(n-Butyl)deoxygalactonojirimycin
Canonical SMILES OC[C@H]1N(CCCC)C[C@H](O)[C@@H](O)[C@H]1O
分子式 C10H21NO4 分子量 219.3
溶解度 DMF: 20 mg/mL,DMSO: 30 mg/mL,Ethanol: 5 mg/mL,PBS (pH 7.2): 10 mg/mL 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 4.56 mL 22.7998 mL 45.5996 mL
5 mM 0.912 mL 4.56 mL 9.1199 mL
10 mM 0.456 mL 2.28 mL 4.56 mL
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Research Update

Novel method for chase analysis of oligosaccharide metabolic error caused by xenobiotics

Anal Biochem 2010 Oct 1;405(1):103-8.PMID:20570645DOI:10.1016/j.ab.2010.06.002.

Saccharide primers, such as dodecyl beta-lactoside (Lac-C12), are unique artificial precursors of glycolipid synthesis. In culture media supplemented with saccharide primers, they are taken up by the cells in the culture media and glycosylated by cellular glycosyltransferases in the Golgi apparatus to form pseudo-glycolipids. In this study, we examine the effects of various xenobiotics on glycolipid synthesis by implementing a novel method to analyze pseudo-glycolipids, mainly gangliosides, produced by ONS-76 medulloblastoma cells in a culture medium containing various xenobiotics. The ganglioside group of pseudo-glycolipids was effectively purified by using strong anion-exchange cartridges. The production of pseudo-gangliosides was stimulated by N-(n-Butyl)deoxygalactonojirimycin (NB-DGJ), but was inhibited by castanospermine, 2-deoxy-2-fluoro-d-galactose, tunicamycin, and brefeldin A. Because the cells in the culture medium are exposed to the saccharide primers and xenobiotics at the same time, and are secreted in the culture medium in their glycosylated form, our method can be used to effectively analyze the direct effects of xenobiotics on ganglioside synthesis.