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Miglustat is an inhibitor of the ceramide-specific glycosyltransferase, which catalyzes the first step of glycosphingolipid biosynthesis and is currently approved for the oral treatment of type I Gaucher disease (GD1). Uses: Enzyme inhibitors. Synonyms: Zavesca; Miglustat; NB-DNJ. Grades: >98%. CAS No. 72599-27-0. Molecular formula: C10H21NO4. Mole weight: 219.28.
Miglustat
Miglustat (N-Butyldeoxynojirimycin) is an orally active and reversible ceramide glucosyltransferase inhibitor. Miglustat can be used for the research of type I gaucher disease [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N-Butyldeoxynojirimycin; NB-DNJ; OGT 918. CAS No. 72599-27-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-17020.
Miglustat HCl
Miglustat HCl is an inhibitor of glucosylceramide synthase, primarily to treat Type I Gaucher disease (GD1). It also inhibits glucosidase I and II, as well as HIV-1 and HIV-2 infection of peripheral blood mononuclear cells (PBMCs). Synonyms: Miglustat hydrochloride. Grades: 98%. CAS No. 210110-90-0. Molecular formula: C10H21NO4 HCl. Mole weight: 255.74.
Miglustat hydrochloride
Miglustat (N-Butyldeoxynojirimycin) hydrochloride is an orally active and reversible ceramide glucosyltransferase inhibitor. Miglustat hydrochloride can be used for the research of type I gaucher disease [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N-Butyldeoxynojirimycin hydrochloride; NB-DNJ hydrochloride; OGT 918 hydrochloride. CAS No. 210110-90-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17020A.
Miglustat O-β-D-Glucuronide is a glucuronide derivative of N-Butyldeoxynojirimycin, an inhibitor of a-glucosidase 1 as well as HIV cytopathicity. N-Butyldeoxynojirimycin has recently been used to retard lipid storage in the central nervous system of an an. Synonyms: (2S,3S,4S,5R,6R)-6-(((2R,3R,4R,5S)-1-Butyl-3,4,5-trihydroxypiperidin-2-yl)methoxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic Acid. Grades: > 95%. Molecular formula: C16H29NO10. Mole weight: 395.4.
2,3,4,6-Tetra-O-benzyl-1-L-ido-miglustat
2,3,4,6-Tetra-O-benzyl-1-L-ido-miglustat is a useful reagent in preparation of pharmaceutically active aza-sugar piperidine derivatives as inhibitors of galactosidase and glucosylceramide synthase. Group: Biochemicals. Grades: Highly Purified. CAS No. 441061-29-6. Pack Sizes: 10mg, 25mg. Molecular Formula: C38H45NO4, Molecular Weight: 579.77. US Biological Life Sciences.
An inhibitor of a-glucosidase 1 as well as being an inhibitor of HIV cytopathicity. N-butyldeoxynojirimycin has recently been used to retard lipid storage in the central nervous system of an animal model of Tay-Sachs disease. Group: Biochemicals. Alternative Names: Miglustat, Hydrochloride. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Lucerastat
Lucerastat, the galactose form of Miglustat, is an orally-available inhibitor of glucosylceramide synthase (GCS). Lucerastat has the potential for Fabry disease study [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NB-DGJ; N-(n-Butyl)deoxygalactonojirimycin. CAS No. 141206-42-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-106392.
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