9AzNue5Ac

Modify Date: 2024-01-14 12:40:48

9AzNue5Ac Structure
9AzNue5Ac structure
Common Name 9AzNue5Ac
CAS Number 76487-51-9 Molecular Weight 334.283
Density N/A Boiling Point N/A
Molecular Formula C11H18N4O8 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of 9AzNue5Ac


9AzNue5Ac, 9-azido-9-deoxy-N-acetylneuraminic acid, is a click chemistry reagent and a Neu5Ac analogue with the substitution of 9-hydroxyl group with an azide. 9AzNue5Ac could be metabolized and incorporated into sialoglycans in living cells and mice. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity[1].

 Names

Name N-Acetyl-9-azido-9-deoxy-neuraminic acid
Synonym More Synonyms

 9AzNue5Ac Biological Activity

Description 9AzNue5Ac, 9-azido-9-deoxy-N-acetylneuraminic acid, is a click chemistry reagent and a Neu5Ac analogue with the substitution of 9-hydroxyl group with an azide. 9AzNue5Ac could be metabolized and incorporated into sialoglycans in living cells and mice. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity[1].
Related Catalog
References

[1]. Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789.  

 Chemical & Physical Properties

Molecular Formula C11H18N4O8
Molecular Weight 334.283
Exact Mass 334.112457
LogP -1.86

 Synonyms

D-glycero-D-galacto-2-Nonulopyranosonic acid, 5-(acetylamino)-9-azido-3,5,9-trideoxy-
(6R)-5-Acetamido-6-[(1R,2R)-3-azido-1,2-dihydroxypropyl]-3,5-dideoxy-L-threo-hex-2-ulopyranosonic acid