
Identification
CAS Number
52050-17-6
Name
Glucosylsphingosine CAS 52050-17-6
Synonyms
(2S,3R,4E)-2-Amino-3-hydroxy-4-octadecen-1-yl β-D-glucopyranoside [ACD/IUPAC Name]
(2S,3R,4E)-2-Amino-3-hydroxy-4-octadecen-1-yl-β-D-glucopyranosid [German] [ACD/IUPAC Name]
1-β-D-Glucosylsphingosine (d18:1)
52050-17-6 [RN]
Glucosylsphingosine
β-D-Glucopyranoside de (2S,3R,4E)-2-amino-3-hydroxy-4-octadécén-1-yle [French] [ACD/IUPAC Name]
β-D-Glucopyranoside, (2S,3R,4E)-2-amino-3-hydroxy-4-octadecen-1-yl [ACD/Index Name]
(2R,3R,4S,5S,6R)-2-[(E,2S,3R)-2-amino-3-hydroxyoctadec-4-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
(2S,3R,4E)-1-O-β-(D-glucopyranosyl)-4-sphingenine
(2S,3R,4E)-2-amino-1-(β-D-glucopyranosyloxy)-4-octadecen-3-ol
(2S,3R,4E)-2-amino-1-(β-D-glucopyranosyloxy)octadec-4-en-3-ol
(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl β-D-glucopyranoside
(2S,3R,4E)-β-D-glucopyranosyl-(1′<->1)-2-amino-4-octadecene-1,3-diol
1-glucosyl-sphing-4-enine
1-β-D-Glucosylsphingosine (d18:1)
1-β-glucosyl-sphing-4-enine
2S-amino-3R-hydroxy-4E-octadecen-1-yl β-D-glucopyranoside
D-Glucosylsphingosine
Glucopsychosine
Glucosphingosine
Glucosyl sphingosine
Lyso GlcCer
lyso-GlcCer
β-D-glucosylsphingosine
SMILES
CCCCCCCCCCCCC/C=C/[C@H]([C@H](CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)N)O
StdInChI
InChI=1S/C24H47NO7/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(27)18(25)17-31-24-23(30)22(29)21(28)20(16-26)32-24/h14-15,18-24,26-30H,2-13,16-17,25H2,1H3/b15-14+/t18-,19+,20+,21+,22-,23+,24+/m0/s1
StdInChIKey
HHJTWTPUPVQKNA-JIAPQYILSA-N
Molecular Formula
C24H47NO7
Molecular Weight
461.633
Beilstein Registry Number
4333674
Properties
Appearance
White Powder
Safety Data
Symbol
Signal Word
Warning
WGK Germany
3
MSDS Download
Specifications and Other Information of Our
Identification Methods
HNMR, HPLC
Purity
95% min
Shelf Life
2 years
Storage
Store at -20°, Sealed and keep dry.
Known Application
Glucosylsphingosine (GlcSph) is a metabolite of sphingolipids and has significant applications in biomedical and clinical research. Glucosylsphingosine is an important biomarker for Gaucher disease, a lysosomal storage disorder caused by a deficiency of the enzyme glucocerebrosidase.
General View of Documents
Links
This product is developed by our R&D company Ulcho Biochemical Limited (http://www.ulcho.com/).
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