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经验公式（希尔记法）:
C37H64D7NO8
化学文摘社编号:
分子量:
665.00
MDL number:
UNSPSC Code:
12352211
NACRES:
NA.12
Assay:
99% (TLC)
Form:
powder
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
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
wgk
WGK 3
法规信息
新产品
此项目有
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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