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Merck

860833P

Avanti

C6(6-azido) GalCer

Avanti Research - A Croda Brand 860833P, powder

别名:

D-galactosyl-β-1,1′ N-(6"-azidohexanoyl)-D-erythro-sphingosine

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About This Item

经验公式(希尔记法):
C30H56 N4O8
分子量:
600.79
分類程式碼代碼:
12352211
NACRES:
NA.25

形狀

powder

包裝

pkg of 1 × 5 mg (860833P-5mg)

製造商/商標名

Avanti Research - A Croda Brand 860833P

脂質類型

click reagents

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC(CCCCCN=[N+]=[N-])=O)CO[C@H](O1)[C@H](O)[C@@H](O)[C@H]([C@H]1CO)O

一般說明

C6(6-azido) GalCer, also known as D-galactosyl-β-1,1′ N-(6"-azidohexanoyl)-D-erythro-sphingosine is a head group modified lipid comprising an omega-terminal azide. The terminal azide group is involved in a highly specific linking reaction with alkyne-containing reagents, known as ‘click chemistry′, in the presence of a copper (Cu)-containing catalyst. Copper-catalyzed azide−alkyne click chemistry plays a vital role in bioconjugation.

包裝

5 mL Amber Glass Screw Cap Vial (860833P-5mg)

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)

No data available

閃點(°C)

No data available


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Stanislav I Presolski et al.
Current protocols in chemical biology, 3(4), 153-162 (2011-01-01)
The copper-catalyzed azide-alkyne cycloaddition reaction is widely used for the connection of molecular entities of all sizes. A protocol is provided here for the process with biomolecules. Ascorbate is used as reducing agent to maintain the required cuprous oxidation state.

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