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 9AzNue5Ac9AzNue5Ac, 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]. |
Name | N-Acetyl-9-azido-9-deoxy-neuraminic acid |
---|---|
Synonym | More Synonyms |
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 |
Molecular Formula | C11H18N4O8 |
---|---|
Molecular Weight | 334.283 |
Exact Mass | 334.112457 |
LogP | -1.86 |
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 |