38229-75-3 Usage
Uses
Used in Research and Development:
4'-IODOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE is used as a research chemical for enhancing plant and bacterial lectin binding affinities. This application is crucial in understanding the molecular mechanisms underlying various biological processes and can potentially lead to the development of new therapeutic strategies.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4'-IODOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE is used as a key intermediate in the synthesis of various glycoconjugates and glycoproteins. These molecules play essential roles in numerous biological processes, including cell adhesion, immune response, and cell signaling, making them important targets for drug development.
Used in Diagnostic Applications:
4'-IODOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE can also be employed in the development of diagnostic tools, such as assays and sensors, that rely on the specific interactions between lectins and their carbohydrate ligands. These diagnostic tools can be used to detect and monitor various diseases and conditions related to altered glycosylation patterns.
Used in Biotechnology:
In the biotechnology sector, 4'-IODOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE can be utilized in the engineering of recombinant proteins with specific glycosylation patterns. This can lead to the development of novel biotherapeutics with improved efficacy, stability, and reduced immunogenicity.
Overall, 4'-IODOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE is a versatile research chemical with a wide range of applications in various industries, including pharmaceuticals, biotechnology, and diagnostics. Its unique properties and potential for enhancing lectin binding affinities make it a valuable tool for advancing our understanding of biological processes and developing new therapeutic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 38229-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,2 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38229-75:
(7*3)+(6*8)+(5*2)+(4*2)+(3*9)+(2*7)+(1*5)=133
133 % 10 = 3
So 38229-75-3 is a valid CAS Registry Number.
38229-75-3Relevant academic research and scientific papers
Carbohydrate protein interactions. Syntheses of agglutination inhibitors of wheat germ agglutinin by phase transfer catalysis
Roy, Rene,Tropper, Francois D.
, p. 817 - 821 (2007/10/02)
Starting from chloride 1, a series of para-substituted aryl 2-acetamido-2-deoxy-β-D-glucopyranosides were prepared using phase transfer catalysis conditions with tetrabutylammonium hydrogen sulfate in 1 M sodium hydroxide and methylene chloride at room temperature.Zemplen de-O-acetylation afforded the unprotected glycosides.Optimization of reaction conditions was evaluated.Several functional group manipulations were effected to widen the number and nature of the para-substituents. Key words: phase transfer catalysis, aryl 2-acetamido-2-deoxy-β-D-glucopyranosides.
