Miglustat is a 1,5-dideoxy-1,5-imino-D-glucitol derivative featuring a six-membered cyclohexane ring substituted with amino, hydroxyl, and acetyl groups. The core structure includes a nitrogen atom at the 1-position and hydroxyl moieties at C2, C3, C4, and C6, with an acetyl group at C6. This compound, identical to its parent drug, exhibits stereochemistry critical for glycosidase inhibition. Its functional groups enable interactions with carbohydrate metabolic pathways. Analytically, Miglustat serves as an HPLC reference standard for pharmaceutical quality control.
On RequestCCCCN1C[C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O
InChI=1S/C10H21NO4/c1-2-3-4-11-5-8(13)10(15)9(14)7(11)6-12/h7-10,12-15H,2-6H2,1H3/t7-,8+,9-,10-/m1/s1
UQRORFVVSGFNRO-UTINFBMNSA-N