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Merck
CN

330728P

Avanti

C13 Galactosyl(β) Ceramide-d7 (d18:1-D7/13:0)

Avanti Research™ - A Croda Brand

Synonym(s):

D-galactosyl-β-1,1′-N-tridecanoyl-D-erythro-sphingosine-d7

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About This Item

Empirical Formula (Hill Notation):
C37H64D7NO8
CAS Number:
2315262-19-0
Molecular Weight:
665.00
MDL number:
MFCD35064284
UNSPSC Code:
12352211
NACRES:
NA.12
Assay:
99% (TLC)
Form:
powder

Key Documents

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InChI

1S/C37H71NO8/c1-3-5-7-9-11-13-15-16-17-18-20-22-24-26-31(40)30(29-45-37-36(44)35(43)34(42)32(28-39)46-37)38-33(41)27-25-23-21-19-14-12-10-8-6-4-2/h24,26,30-32,34-37,39-40,42-44H,3-23,25,27-29H2,1-2H3,(H,38,41)/b26-24+/t30-,31+,32+,34-,35-,36+,37+/m0/s1/i1

InChI key

KJMFYHPLIHBVNV-SXOXVQABSA-N

SMILES string

[H][C@](/C=C/CCCCCCCCCCC([2H])([2H])C([2H])([2H])C([2H])([2H])[2H])(O)[C@@]([H])(NC(CCCCCCCCCCCC)=O)CO[C@H](O1)[C@H](O)[C@@H](O)[C@@H](O)[C@H]1CO

assay

99% (TLC)

form

powder

packaging

pkg of 1 × 1 mg (330728P-1MG)

manufacturer/tradename

Avanti Research™ - A Croda Brand

shipped in

dry ice

storage temp.

−20°C

General description

C13 Galactosyl(β) Ceramide-d7 (d18:1-D7/13:0) is deuterated derivative of C13 Galactosyl(β) Ceramide. β-Galactosyl ceramide (β −GalCer) is one of the uncomplicated glycosphingolipid. It contains a lipophilic sphingosine and a hydrophilic galactose moiety, which is attached to sphingosine via an ether linkage. It is localized in the myelin sheath of the peripheral and central nervous system.

Biochem/physiol Actions

β-Galactosyl ceramide (β −GalCer) plays a role in regulating the activity of β-glucocerebrosidase (β-GlcCer′ase). It is also a receptor for various bacterial and viral toxins.

Packaging

5 mL Amber Glass Screw Cap Vial

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

wgk

WGK 3

Regulatory Information

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Design, synthesis, and evaluation of beta-galactosylceramide mimics promoting beta-glucocerebrosidase activity in keratinocytes
Fukunaga K, et al.
Bioorganic & Medicinal Chemistry Letters, 13(5), 813-815 (2003)

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