Comparison

Lucerastat European Partner

Item no. TMO-T32923-500mg
Manufacturer TargetMol
CASRN 141206-42-0
Amount 500 mg
Quantity options 100 mg 25 mg 500 mg 50 mg 5 mg
Category
Type Chemicals
Specific against other
Formula C10H21NO4
Smiles C(CCC)N1[C@H](CO)[C@H](O)[C@H](O)[C@@H](O)C1
ECLASS 10.1 32160000
ECLASS 11.0 32160000
UNSPSC 12000000
Alias NB DGJ,N-(n-Butyl)deoxygalactonojirimycin,ACT 434964,NBDGJ,OGT 923
Shipping Condition Cool pack
Available
Manufacturer - Targets
Transferase
Shipping Temperature
Cool pack
Storage Conditions
-20
Molecular Weight
219.28
Description
Lucerastat(NBDGJ) is an orally available inhibitor of Glucosylceramide Synthase (GCS) with therapeutic potential for Fabry disease. GCS is a key enzyme in sphingolipid synthesis and inhibition of its activity reduces the accumulation of harmful substrates.
Pathways
Metabolism
Bioactivity
Lucerastat is a very effective and selective α-gal A (α-D-galactosidase) inhibitor for the treatment of lipid storage diseases and Fabry disease.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 500 mg
Available: In stock
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