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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-[d9] hydrochloride
Miglustat-[d9] hydrochloride is a labelled Miglustat Hydrochloride which is an inhibitor of a-glucosidase 1 as well as being an inhibitor of HIV cytopathicity. Synonyms: N-Butyldeoxynojirimycin Hydrochloride-d9; (2R,3R,4R,5S)-1-Butyl-2-(hydroxymethyl)-,3,4,5-Piperidinetriol Hydrochloride-d9. Grade: > 95%. CAS No. 1883545-57-0. Molecular formula: C10H13D9ClNO4. Mole weight: 264.79.
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.
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.
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Benzyl Miglustat hydrochloride
An impurity of Miglustat. Miglustat is an oral ceramide glucosyltransferase inhibitor used to treat mild to moderate type 1 Gaucher disease in adults who cannot undergo enzyme replacement therapy due to allergies, hypersensitivity, or other limitations. Synonyms: Piperidine, 1-butyl-3,4,5-tris(phenylmethoxy)-2-[(phenylmethoxy)methyl]-, hydrochloride (1:1), (2R,3R,4R,5S)-; (2R,3R,4R,5S)-1-Butyl-3,4,5-tris(phenylmethoxy)-2-[(phenylmethoxy)methyl]piperidine hydrochloride; Tetrabenzyl Miglustat hydrochloride; N-Boc-tetra-O-benzyl-1-deoxynojirimycin hydrochloride; N-Butyl 2,3,4,6-tetra-O-benzyl-1,5-dideoxy-1,5-imino-D-glucitol hydrochloride; (2R,3R,4R,5S)-3,4,5-Tris(benzyloxy)-2-(benzyloxymethyl)-1-butylpiperidine hydrochloride. Grade: ≥95%. CAS No. 1938122-78-1. Molecular formula: C38H46ClNO4. Mole weight: 616.24.
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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