168397-51-1 Usage
Description
2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE is a glucopyranosyl azide derivative that features an acetamido group and a benzylidene moiety. This chemical compound is of interest in the field of medicinal chemistry and drug development due to its potential applications in the synthesis of glycoconjugates and glycopeptides, as well as its activity as a glycosyl donor in chemical reactions. It has also been investigated for its potential biological interactions and therapeutic applications, showing promise in various research areas.
Used in Medicinal Chemistry:
2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE is used as a key intermediate in the synthesis of complex carbohydrate structures for medicinal chemistry applications. Its unique structure allows for the creation of novel glycoconjugates and glycopeptides that can be used in the development of new drugs and therapeutic agents.
Used in Drug Development:
In the pharmaceutical industry, 2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE is utilized as a glycosyl donor in chemical reactions, facilitating the synthesis of bioactive compounds with potential therapeutic properties. Its role in these reactions is crucial for the development of innovative drug candidates.
Used in Glycobiology Research:
2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE is employed as a research tool in glycobiology to study the biological interactions of carbohydrates with proteins and other biomolecules. Understanding these interactions can lead to insights into the role of carbohydrates in various diseases and the development of targeted therapies.
Overall, 2-ACETAMIDO-4,6-O-BENZYLIDENE-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE is a versatile chemical compound with a range of applications in the fields of medicinal chemistry, drug development, and glycobiology research. Its potential for further exploration and development into new drugs and therapeutic agents is significant.
Check Digit Verification of cas no
The CAS Registry Mumber 168397-51-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,3,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 168397-51:
(8*1)+(7*6)+(6*8)+(5*3)+(4*9)+(3*7)+(2*5)+(1*1)=181
181 % 10 = 1
So 168397-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H18N4O5/c1-8(20)17-11-12(21)13-10(23-14(11)18-19-16)7-22-15(24-13)9-5-3-2-4-6-9/h2-6,10-15,21H,7H2,1H3,(H,17,20)/t10-,11-,12-,13-,14-,15-/m1/s1
168397-51-1Relevant articles and documents
Synthesis and self-assembling properties of 4,6?O-benzylidene acetal protected D-glucose and D-glucosamine β?1,2,3?triazole derivatives
Chen, Anji,Okafor, Ifeanyi S.,Garcia, Consuelo,Wang, Guijun
, p. 60 - 75 (2018)
Sugar based low molecular weight gelators (LMWGs) are useful small molecules that can form reversible supramolecular gels with many applications. Selective functionalization of common monosaccharides has resulted in several classes of effective LMWGs. Rec
Endo-β-N-Acetylglucosaminidase catalysed glycosylation: Tolerance of enzymes to structural variation of the glycosyl amino acid acceptor
Tomabechi, Yusuke,Squire, Marie A.,Fairbanks, Antony J.
, p. 942 - 955 (2014/02/14)
Endo-β-N-Acetylglucosaminidases (ENGases) are highly useful biocatalysts that can be used to synthetically access a wide variety of defined homogenous N-linked glycoconjugates in a convergent manner. The synthetic efficiency of a selection of family GH85
Combinatorial libraries of monosaccharides
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Page 18, (2010/02/05)
A monosaccharide compound of formula I as shown in the specification. Processes for the preparation of the compound of formula I and methods of screening for antibacterial or antibiotic compounds involving the compound of formula I.
