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Merck

330728P

Avanti

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

Avanti Research - A Croda Brand

别名:

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

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About This Item

经验公式(希尔记法):
C37H64D7NO8
分子量:
665.00
分類程式碼代碼:
12352211
NACRES:
NA.12

化驗

99% (TLC)

形狀

powder

包裝

pkg of 1 × 1 mg (330728P-1MG)

製造商/商標名

Avanti Research - A Croda Brand

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[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

一般說明

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.

生化/生理作用

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.

包裝

5 mL Amber Glass Screw Cap Vial

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

儲存類別代碼

11 - Combustible Solids

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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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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