Name | (2S,3R,4E)-3-Hydroxy-2-({12-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]dodecanoyl}amino)-4-octadecen-1-yl 2-(trimethylammonio)ethyl phosphate |
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Synonyms |
(2S,3R,4E)-3-Hydroxy-2-({12-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]dodecanoyl}amino)-4-octadecen-1-yl 2-(trimethylammonio)ethyl phosphate
Ethanaminium, 2-[[hydroxy[[(2S,3R,4E)-3-hydroxy-2-[[12-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-1-oxododecyl]amino]-4-octadecen-1-yl]oxy]phosphinyl]oxy]-N,N,N-trimethyl-, inner salt |
Description | C12 NBD sphingomyelin is an active derivative of sphingomyelin (HY-113498) that is tagged with fluorescent C12 nitrobenzoxadiazole (C12 NBD). C12 NBD sphingomyelin can be used as a sphingomyelinase substrate for studying the metabolism and transport of sphingomyelins (Ex=470 nm, Em=525 nm)[1]. |
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Related Catalog | |
Target |
Sphingomyelinase[1] |
In Vitro | Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs)[1]. Assay for Sphingolipid-Degrading Enzymes (EGCase Ⅱ, SCDase and SMase): 1. Incubate amounts of enzymes with 0.1 nM dye at 37 ℃ for indicated times under following conditions. (1). 10 mM sodium acetate buffer (pH5.0) containing 0.2% Triton X-100 for EGCase. (2) 25 mM sodium phosphate buffer (pH 6.0) containing 0.1% Triton X-100 for SCDase. (3) 25 mM sodium phosphate buffer (pH 7.0) containing 0.2% Triton X-100 for SMase. 2. After incubation, the solvent is evaporated and the residue is dried, dissolved in 10 μL of chloroform/methanol (2:1) and analyzed by TLC using chloroform/methanol/0.02% CaCl2 (5:4:1, v/v) as the developing solvent. 3. Degradation products and remaining substrates are separated by TLC and quantified with a chromatoscanner (excitation 470 nm, emission 525 nm) for fluorescence-labeled substrates. |
References |
Molecular Formula | C41H73N6O9P |
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Molecular Weight | 825.027 |
Exact Mass | 824.517639 |
LogP | 7.63 |