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810211P

Avanti

C12-NBD Ceramide

Avanti Research - A Croda Brand 810211P, powder

Sinónimos:

N-[12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl]-D-erythro-sphingosine

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1 MG
US$ 710,00

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1 MG
US$ 710,00

About This Item

Fórmula empírica (notación de Hill):
C36H61N5O6
Número de CAS:
Peso molecular:
659.90
Número MDL:
Código UNSPSC:
12352211
NACRES:
NA.25

US$ 710,00

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Ensayo

>99% (TLC)

Formulario

powder

envase

pkg of 1 × 1 mg (810211P-1mg)

fabricante / nombre comercial

Avanti Research - A Croda Brand 810211P

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

cadena SMILES

[N+](=O)([O-])c1c2n[o]nc2c(cc1)NCCCCCCCCCCCC(=O)N[C@H]([C@H](O)\C=C\CCCCCCCCCCCCC)CO

InChI

1S/C36H61N5O6/c1-2-3-4-5-6-7-8-9-10-12-15-18-21-24-33(43)31(29-42)38-34(44)25-22-19-16-13-11-14-17-20-23-28-37-30-26-27-32(41(45)46)36-35(30)39-47-40-36/h21,24,26-27,31,33,37,42-43H,2-20,22-23,25,28-29H2,1H3,(H,38,44)/b24-21+/t31-,33+/m0/s1

Clave InChI

SNOJCYCOPNIGIK-ULETYAGTSA-N

Descripción general

C12 7-nitro-2-1,3-benzoxadiazol-4-yl (NBD) ceramide is a long-chain fluorescent phospholipid.[1] It is a natural analog of ceramide with C12 acyl chain length.[2]

Aplicación

C12-NBD Ceramide or N-[12-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]dodecanoyl]-D-erythro-sphingosine has been used as a substrate in ceramidase activity assay.[3] It is also suitable for the lipid binding assays[4] and in cell culture experiments for endothelial cells to determine the pro-apoptotic intracellular ceramide generation.[5]

Acciones bioquímicas o fisiológicas

C12-7-nitro-2-1,3-benzoxadiazol-4-yl (NBD) Ceramide is useful for measuring the alkaline and neutral ceramidase activity.[1] It is involved in maintainingthe physical properties of ceramide required for cellular studies.[2]

Envase

5 mL Amber Glass Screw Cap Vial (810211P-1mg)

Información legal

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Código de clase de almacenamiento

11 - Combustible Solids


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Effect of ceramide N-acyl chain and polar headgroup structure on the properties of ordered lipid domains (lipid rafts)
Meghan PS, et al.
Biochimica et Biophysica Acta, 1768(9), 2205-2212 (2007)
M Tani et al.
Journal of biochemistry, 125(4), 746-749 (1999-04-02)
A fluorescent analogue of ceramide, C12-NBD-ceramide, was found to be hydrolyzed much faster than 14C-labeled ceramide by alkaline ceramidase from Pseudomonas aeruginosa and neutral ceramidase from mouse liver, while this substrate was relatively resistant to acid ceramidase from plasma of
Terry R Medler et al.
American journal of respiratory cell and molecular biology, 38(6), 639-646 (2008-01-15)
The de novo pathway of ceramide synthesis has been implicated in the pathogenesis of excessive lung apoptosis and murine emphysema. Intracellular and paracellular-generated ceramides may trigger apoptosis and propagate the death signals to neighboring cells, respectively. In this study we
VPS13A and VPS13C are lipid transport proteins differentially localized at ER contact sites
Nikit K, et al.
The Journal of Cell Biology, 217(10), 3625-3639 (2018)
Apoptotic Sphingolipid Signaling by Ceramides in Lung Endothelial Cells
Medler TR, et al.
American Journal of Respiratory Cell and Molecular Biology, 38(6), 639-646 (2008)

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