UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
B B B0 B1 B4 B7 B8 BA BB BC BD BE BF BG BH BI BK BL BM BN BO BP BR BS BT BU BV BW BX BY BZ
BUB BUC BUD BUE BUF BUG BUI BUL BUM BUN BUP BUR BUS BUT BUV

1,5-(butylimino)-1,5-dideoxy-D-glucitol

[A synthetic, N-alkylated imino analogue of D-glucose. Miglustat competitively and reversibly binds to and inhibits the activity of UDP-glucose ceramide glucosyltransferase, which catalyzes the initial step in the synthesis of glycosphingolipids (GSL). This leads to a decrease in the production of glycosphingolipid, which has important roles in various cellular processes. Miglustat can be used in substrate reduction therapy in diseases in which the enzyme glucocerebrosidase, that is responsible for the breakdown of GSL, is deficient. ( NCI )]
UMLS (NCI) C1321596
3,4,5-Piperidinetriol, 1-butyl-2-(hydroxymethyl)-,(2R-(2alpha,3beta,4alpha,5beta))-
MIGLUSTAT
MIGLUSTAT PREPARATION
N-Butyl Deoxynojirimycin
N-Butylmoranoline
 
Organic Chemical
Pharmacologic Substance
Relation/PAR: [HS900] HORMONES/SYNTHETICS/MODIFIERS, OTHER
Unclassified Ingredients
Relation/CHD: MIGLUSTAT 100 MG

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