57467-13-7 Usage
Uses
1. Organic Synthesis:
BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P is used as a synthetic building block for the creation of various complex carbohydrates and glycoconjugates. Its unique structure allows for the development of novel compounds with potential applications in various fields, such as pharmaceuticals, biotechnology, and materials science.
2. Pharmaceutical Applications:
In the pharmaceutical industry, BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P can be used as a key intermediate in the synthesis of glycoconjugate drugs, which have the potential to target specific biological receptors and modulate cellular processes. These drugs can be employed for the treatment of various diseases, including cancer, inflammatory disorders, and infectious diseases.
3. Biotechnology Applications:
In the biotechnology sector, BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P can be utilized in the development of glyco-engineered proteins and enzymes. These glyco-engineered biomolecules can exhibit improved stability, solubility, and bioactivity, making them valuable tools for research and therapeutic applications.
4. Materials Science Applications:
BETA-D-GAL-(1->3)-BETA-D-GLCNAC-1->OC6H4NO2-P can also be employed in the field of materials science for the design and synthesis of carbohydrate-based materials, such as hydrogels, nanoparticles, and self-assembled structures. These materials can find applications in drug delivery, tissue engineering, and sensing technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 57467-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,6 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57467-13:
(7*5)+(6*7)+(5*4)+(4*6)+(3*7)+(2*1)+(1*3)=147
147 % 10 = 7
So 57467-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H28N2O13/c1-8(25)21-13-18(35-20-17(29)16(28)14(26)11(6-23)34-20)15(27)12(7-24)33-19(13)32-10-4-2-9(3-5-10)22(30)31/h2-5,11-20,23-24,26-29H,6-7H2,1H3,(H,21,25)
57467-13-7Relevant academic research and scientific papers
Facile preparation of indoxyl- and nitrophenyl glycosides of lactosamine and isolactosamine
Boettcher, Stephan,Thiem, Joachim
, p. 10856 - 10861 (2014/03/21)
The synthesis of the novel indoxyl glycosides of N-acetyl-lactosamine (X-LacNAc) and N-acetyl-isolactosamine (X-LNB) is reported employing glycosyl chlorides in a facile phase transfer glycosylation, followed by mild decarboxylation and finally deacetylat
Characterization and synthetic application of a novel β1,3-galactosyltransferase from Escherichia coli O55:H7
Liu, Xian-wei,Xia, Chengfeng,Li, Lei,Guan, Wan-yi,Pettit, Nicholas,Zhang, Hou-cheng,Chen, Min,Wang, Peng George
experimental part, p. 4910 - 4915 (2009/11/30)
A β1,3-galactosyltransferase (WbgO) was identified in Escherichia coli O55:H7. Its function was confirmed by radioactive activity assay and structure analysis of the disaccharide synthesized with the recombinant enzyme. WbgO requires a divalent metal ion,
Enhanced enzymatic reactions in a microchannel reactor
Kanno, Kenichi,Kawazumi, Hirofumi,Miyazaki, Masaya,Maeda, Hideaki,Fujii, Masayuki
, p. 687 - 690 (2007/10/03)
Organic and enzymatic reactions in microchannel reactors were discussed. Hydrolytic activity of a microchannel pre-treated with enzyme solution was studied. It was found that the reaction rate in microchannel is much faster than the micro test tube. Mass transfer is also much more efficient in microchannel.
Regioselective synthesis of p-nitrophenyl glycosides of β-D-galactopyranosyl-disaccharides by transglycosylation with β-D-galactosidases
Zeng, Xiaoxiong,Yoshino, Rika,Murata, Takeomi,Ajisaka, Katsumi,Usui, Taichi
, p. 120 - 131 (2007/10/03)
The β-D-galactosidase from porcine liver induced regiospecific transglycosylation of β-D-galactose from β-D-Gal-OC6H4NO2-o to OH-6 of, respectively, p-nitrophenyl glycoside acceptors of Gal, GlcNAc and GalNAc to afford β-G
