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Catalog Number:
32367
CAS Number:
84380-10-9
4,7,8,9-tétra -O -acétyl- N -acétylneuraminate de méthyle
Purity:
≥ 95 % (dosage)
Synonym(s):
Ester méthylique de l'acide 4,7,8,9-tétra- O -acétyl -N -acétylneuraminique, Ester méthylique de l'acide N -acétylneuraminique4,7,8,9-tétraacétate
Documents
$79.22 /100 mg
Taille
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Product Information

Conserver à l'abri des agents oxydants.

Synonyms
Ester méthylique de l'acide 4,7,8,9-tétra- O -acétyl -N -acétylneuraminique, Ester méthylique de l'acide N -acétylneuraminique4,7,8,9-tétraacétate
CAS Number
84380-10-9
Purity
≥ 95 % (dosage)
Molecular Formula
C 20 H 2913
Molecular Weight
491.44
MDL Number
MFCD08276266
PubChem ID
14376169
Melting Point
185 - 189°C
Appearance
Poudre cristalline blanche à beige pâle
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Ester méthylique de l'acide 4,7,8,9-tétra- O -acétyl -N -acétylneuraminique, Ester méthylique de l'acide N -acétylneuraminique4,7,8,9-tétraacétate
CAS Number
84380-10-9
Purity
≥ 95 % (dosage)
Molecular Formula
C 20 H 2913
Molecular Weight
491.44
MDL Number
MFCD08276266
PubChem ID
14376169
Melting Point
185 - 189°C
Appearance
Poudre cristalline blanche à beige pâle
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Methyl 4,7,8,9-tetra-O-acetyl-N-acetylneuraminate is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a valuable substrate in studies investigating sialic acid metabolism and its role in cellular interactions, particularly in the context of viral infections and immune responses.
  • Vaccine Development: It is used in the formulation of vaccines, where its sialic acid derivatives can enhance the immunogenicity of antigens, improving vaccine efficacy against various pathogens.
  • Drug Design: Researchers leverage its structural properties to design inhibitors targeting sialidases, which are enzymes involved in the pathogenicity of several viruses and bacteria.
  • Glycobiology: This compound aids in the study of glycoproteins and glycolipids, helping scientists understand their functions in cell signaling and recognition processes.
  • Diagnostic Applications: It is utilized in the development of diagnostic assays for detecting sialic acid-related diseases, providing insights into conditions such as cancer and neurodegenerative disorders.

Citations