ChemicalBook--->CAS DataBase List--->76204-02-9

76204-02-9

76204-02-9 Structure

76204-02-9 Structure
IdentificationBack Directory
[Name]

2'-(4-METHYLUMBELLIFERYL)-ALPHA-D-N-ACETYLNEURAMINIC ACID SODIUM SALT
[CAS]

76204-02-9
[Synonyms]

NEU5AC-A-4MU
4-MU-NANA NA
Neu5Ac-α-4MU
NEU5AC-ALPHA-4MU SODIUM SALT
2-(4-methylumbelliferyl)-A-D-N-*acetylneuraminic
2-(4-methylumbelliferyl)-α-D-N-*acetylneuraminic
2'-(4-METHYLUMBELLIFERYL)-A-D-N-*ACETYLN EURAMINIC A
4-methylumberiferryl-N-acetyl-alpha-D-neuraminic acid Na
4-MethylumbelliferylN-acetyl-a-D-neuraminicacidsodiumsalt
4-methylumbelliferyl-N-acetyl-alpha-D-neuram.A.so-S.dihy.
4-Methylumbelliferyl N-acetyl-α-D-neuraminic acid sodium salt
4-Methylumbelliferyl-N-acetyl-alpha-D-neuraminic acid sodium salt
2'-(4-METHYLUMBELLIFERYL)-A-D-N-ACETYLNEURAMINIC ACID, SODIUM SALT
2'-(4-Methylumbelliferyl)-α-D-N-acetylneuraminic Acid, Sodium Salt
4-Methylumbelliferyl N-acetyl-a-D-neuraminic acid sodium salt ,97%
2'-(4-METHYLUMBELLIFERYL)-ALPHA-D-N-ACETYLNEURAMINIC ACID SODIUM SALT
4-methylumbelliferyl-n-acetyl-α-d-neuraminic acid sodium salt hydrate
4-Methylumbelliferyl-N-acetyl-a-D-neuraminic acid Sodium salt Dihydrate
2'-(4-METHYLUMBELLIFERYL)-A-D-N-ACETYLNEURAMINIC ACID SODIUM SALT HYDRATE
2'-(4-methylumbelliferyl)-α-d-n-acetylneuraminic acid sodium salt hydrate
4-Methylumbelliferyl-N-acetyl-α-D-neuraminic acid hydrate sodium salt
2μ-(4-Methylumbelliferyl)-α-D-N-acetylneuraminic acid hydrate sodium salt
2'-(4-Methylumbelliferyl)-alpha-D-N-acetylneuraminic acid sodium salt hydrate
N-Acetyl-2-O-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-alpha-neuraminic acid monosodium salt
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C21H24NNaO11
[MDL Number]

MFCD00057309
[MOL File]

76204-02-9.mol
[Molecular Weight]

489.41
Chemical PropertiesBack Directory
[Appearance]

Off-White to Yellow Solid
[Melting point ]

171°C dec.
[storage temp. ]

−20°C
[solubility ]

H2O: 50 mg/mL, clear, very slightly yellow
[form ]

Solid
[color ]

White to Off-White
[Water Solubility ]

water: 50mg/mL, clear to slightly hazy, colorless to light yellow
[InChIKey]

NSQMRVBWXQQIKF-NVRWCLOTSA-M
[SMILES]

O.[H]C(O)(CO)[C@]([H])(O)[C@@H]1OC(C[C@H](O)[C@H]1NC(C)=O)(Oc2ccc3C(C)=CC(=O)Oc3c2)C(=O)O[Na]
Hazard InformationBack Directory
[Chemical Properties]

Off-White to Yellow Solid
[Uses]

This compound has been used for fluorometric assay of neuraminidase as well as fluorescent staining of sialidases in PAGE.
[Uses]

Used as a substrate in a fluorometric assay of neuraminidase.
[Description]

4-Methylumbelliferyl-N-acetyl-α-D-neuraminic acid is a fluorogenic substrate of neuraminidases. 4-Methylumbelliferyl-N-acetyl-α-D-neuraminic acid is cleaved by neuraminidases to release the fluorescence moiety 4-methylumbelliferyl (4-MU). 4-MU fluorescence is pH-dependent with excitation maxima of 320 and 360 nm at low (1.97-6.72) and high (7.12-10.3) pH, respectively, and an emission maximum ranging from 445 to 455 nm, increasing as pH decreases. 4-Methylumbelliferyl-N-acetyl-α-D-neuraminic acid has been used to quantify neuraminidase activity in mammalian cells and clinical isolates of influenza virus.
[Biochem/physiol Actions]

Substrate for fluorometric assay of neuraminidase. Used for fluorescent staining of sialidases in PAGE.
[References]

[1] E MONTI. Expression of a novel human sialidase encoded by the NEU2 gene.[J]. Glycobiology, 1999, 9 12: 1313-1321. DOI: 10.1093/glycob/9.12.1313
[2] NICHOLAS M STAMATOS. Differential expression of endogenous sialidases of human monocytes during cellular differentiation into macrophages.[J]. FEBS Journal, 2005, 272 10: 2545-2556. DOI: 10.1111/j.1742-4658.2005.04679.x
[3] ALAN S CROSS. NEU1 and NEU3 sialidase activity expressed in human lung microvascular endothelia: NEU1 restrains endothelial cell migration, whereas NEU3 does not.[J]. The Journal of Biological Chemistry, 2012: 15966-15980. DOI: 10.1074/jbc.m112.346817
[4] N T WETHERALL. Evaluation of neuraminidase enzyme assays using different substrates to measure susceptibility of influenza virus clinical isolates to neuraminidase inhibitors: report of the neuraminidase inhibitor susceptibility network.[J]. Journal of Clinical Microbiology, 2003, 41 2: 742-750. DOI: 10.1128/jcm.41.2.742-750.2003
Safety DataBack Directory
[Safety Statements ]

24/25
[WGK Germany ]

3
[F ]

3-10
[HS Code ]

29322090
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

(4-Methylumbelliferyl)-N-acetyl-α-D-neuraminic acid sodium salt(76204-02-9)1HNMR
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