1093733-24-4 Usage
Description
N-Biotinyl D-erythro-Sphingosine-1-phosphate is a biotinylated substrate conjugate that plays a significant role in various biochemical processes and applications. It is particularly useful in the field of research and diagnostics due to its unique properties and functions.
Uses
Used in Research and Diagnostics:
N-Biotinyl D-erythro-Sphingosine-1-phosphate is used as a biotinylated substrate for performing enzyme-linked immunosorbent assay (ELISA) on water-soluble ligands. This application is crucial for the detection and quantification of specific molecules in biological samples, contributing to the advancement of scientific research and the development of diagnostic tools.
Used in Ceramide Phosphate Sphingosine Synthesis:
In the field of biochemistry, N-Biotinyl D-erythro-Sphingosine-1-phosphate is utilized as a key component in the synthesis of ceramide phosphate sphingosine. This molecule has essential roles in cellular processes, including cell signaling and the regulation of various biological functions. The use of N-Biotinyl D-erythro-Sphingosine-1-phosphate in this context aids in understanding the complex mechanisms underlying these processes and can potentially lead to the development of novel therapeutic strategies for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 1093733-24-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,7,3 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1093733-24:
(9*1)+(8*0)+(7*9)+(6*3)+(5*7)+(4*3)+(3*3)+(2*2)+(1*4)=154
154 % 10 = 4
So 1093733-24-4 is a valid CAS Registry Number.
1093733-24-4Relevant articles and documents
An efficient, one-pot synthesis of various ceramide 1-phosphates from sphingosine 1-phosphate
Nussbaumer, Peter,Hornillos, Valentin,Ghobrial, Michael,Ullrich, Thomas
, p. 125 - 128 (2008/09/16)
An efficient, one-pot procedure for the synthesis of ceramide 1-phosphates with varying N-acyl substituents, to serve as tool compounds for analytical and biological investigations, was developed. Sphingosine 1-phosphate was silylated in situ to increase its solubility and to protect the 3-hydroxy functionality and then allowed to react with activated acid derivatives in the presence of diisopropylethylamine. Simultaneous cleavage of the silyl protecting groups and separation from reagents and by-products was achieved by medium pressure chromatography on reversed phase material. Thus, ceramide 1-phosphates with various fatty acid chains and with fluorescent and affinity labels attached to the sphingoid backbone were prepared in good yields.
