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Lucerasta is the galactose form of Miglustat, an orally active inhibitor of glucosylceramide synthase (GCS).Lucerastat has potential for use in Fabry disease research.
| Molecular Weight | 219.28 |
| Formula | C10H21NO4 |
| CAS Number | 141206-42-0 |
| Storage | -20°C, dry, sealed |
[1] Frank Weidemann, et al. Int J Mol Sci. Chaperone Therapy in Fabry Disease
[2] Malte Lenders, et al. Drugs. Fabry Disease: The Current Treatment Landscape
[4] M Michaud, et al. Rev Med Interne. [Fabry disease: A review]
[5] Sanne J van der Veen, et al. J Inherit Metab Dis. Developments in the treatment of Fabry disease
| Related Glucosylceramide Synthase Products |
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| DL-threo-PDMP hydrochloride
DL-threo-PDMP hydrochloride is the hydrochloride form of DL-threo-PDMP that is a competitive glucosylceramide synthase (GCS) inhibitor. |
| G43
G43 is a potent, selective glucosyltransferase inhibitor, with the Kd of 3.7μM and 46.9 nM for GtfB and GtfC, respectively. |
| Glucosylceramide synthase-IN-1
Glucosylceramide synthase-IN-1 (T-036) a potent, brain-penetrant and orally active glucosylceramide synthase (GCS) inhibitor with IC50s of 31 nM and 51 nM for human GCS and mouse GCS, respectively. Glucosylceramide synthase-IN-1 can be used for Gaucher's disease research. |
| D-threo-PDMP
D-threo-PDMP is a potent glucoceramide synthase (GCS) inhibitor, which reduces the glycosphingolipids on the cell surface by inhibiting glycosylation, reduces the total length of the axon plexus and the number of axon branch points, and inhibits neurite growth. |
| Glucosylceramide synthase-IN-2
Glucosylceramide-IN-2 (T-690) is a potent, blood-brain barrier-transparent and orally active inhibitor of glucosylceramide synthase (GCS) with IC50s of 15 nM and 190 nM for human GCS and mouse GCS, respectively. basal and non-competitive with UDP-glucose. |
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