N-Acetyl-2-deoxy-2-azido-alpha-neuraminic Acid

Reagent Code: #60452
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CAS Number 202343-12-2

science Other reagents with same CAS 202343-12-2

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Weight 334.29 g/mol
Formula C₁₁H₁₈N₄O₈
inventory_2 Storage & Handling
Storage -20°C

description Product Description

N-Acetyl-2-deoxy-2-azido-alpha-neuraminic acid is primarily used in glycobiology research for the study of sialic acid metabolism and its role in cellular processes. It serves as a key intermediate in the synthesis of sialic acid analogs, which are valuable tools for probing sialyltransferase activity and understanding sialic acid-mediated interactions in biological systems. This compound is also utilized in the development of glycan-based vaccines and therapeutics, as it can be incorporated into glycoconjugates to modulate immune responses. Additionally, its azido group enables click chemistry applications, facilitating the labeling and visualization of sialic acid-containing molecules in cells and tissues.

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inventory 1mg
10-20 days ฿6,372.00

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N-Acetyl-2-deoxy-2-azido-alpha-neuraminic Acid
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N-Acetyl-2-deoxy-2-azido-alpha-neuraminic acid is primarily used in glycobiology research for the study of sialic acid metabolism and its role in cellular processes. It serves as a key intermediate in the synthesis of sialic acid analogs, which are valuable tools for probing sialyltransferase activity and understanding sialic acid-mediated interactions in biological systems. This compound is also utilized in the development of glycan-based vaccines and therapeutics, as it can be incorporated into glycoco

N-Acetyl-2-deoxy-2-azido-alpha-neuraminic acid is primarily used in glycobiology research for the study of sialic acid metabolism and its role in cellular processes. It serves as a key intermediate in the synthesis of sialic acid analogs, which are valuable tools for probing sialyltransferase activity and understanding sialic acid-mediated interactions in biological systems. This compound is also utilized in the development of glycan-based vaccines and therapeutics, as it can be incorporated into glycoconjugates to modulate immune responses. Additionally, its azido group enables click chemistry applications, facilitating the labeling and visualization of sialic acid-containing molecules in cells and tissues.

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