N-Acetylneuraminic acid CAS NO.131-48-6

[Chinese]

N-acetyl neuraminic acid

"English name"

5 - ACETAMIDO - 3, 5 - DIDEOXY - D - GLYCERO - D - GALACTO - 2 - NONU

5 - ACETAMIDO - 3, 5 - DIDEOXY - D - GLYCERO - D - GALACTO - 2 - NONULOSONIC ACID

5 - ACETAMIDO - 3, 5 - DIDEOXY - D - GLYCERO - D - GALACTO - NONULOPYRANOSONIC ACID HYDRATE

5 - ACETAMIDO - 3, 5 - DIDEOXY - D - GLYCERO - D - GALACTONONULOSONIC ACID

5 - ACETAMIDO - 3, 5 - DIDEOXY - D - GLYCERO - D - GALACTONULOSONIC ACID

5 - ACETYLAMINO - 3, 5 - DIDEOXY - D - GLYCERO - D - GALACTO - 2 - NONULOSONIC ACID

ACETYLNEURAMINIC ACID, N -

Galactononulosonic acid

LACTAMINIC ACID

N-[1-13C]ACETYL-D-NEURAMINIC ACID
N-ACETYL-D-NEURAMINIC ACID
(-)-N-ACETYLNEURAMIC ACID
N-ACETYL-NEURAMIC ACID
(-)-N-ACETYLNEURAMINIC ACID
N-(-)-ACETYLNEURAMINIC ACID
N-ACETYLNEURAMINIC ACID
N-ACETYLNEURAMINIC ACID, BOVINE MILK
N-ACETYLNEURAMINIC ACID DIHYDRATE
N-ACETYLNEURAMINIC ACID HYDRATE
N-ACETYLNEURAMINIC ACID TYPE IV-S

"CAS"

 

131-48-6

"Chinese name"

 

N-acetyl neuraminic acid

Sialic acid

N - acetyl neuraminic acid (sialic acid)

Vinegar new pull acid

N-acetyl mannose amine pyruvic acid

N-acetyl sialic acid

Oxygen - sialic acid

N-acetyl - nerve ammonia acid (sugar)

N-acetyl - D - neuraminic acid

N - the flexometallic nerve amino sugar acid

【 EINECS number 】

205-023-1

【 molecular formula 】

C11H19NO9

 

Sialic acid is widely exists in the nature of carbohydrates, also many peptide glycoproteins, candy and basic component of sugar, fat, has extensive biological functions, such as the regulation of blood protein half-life, and a variety of toxins, cell adhesion, immune antigen antibody response and the protection of cytolysis. Sialic acid biochemical derivatives are often used for drug synthesis. N-acetyl neuraminic acid, N - acetylneuraminicacid sialic acid (N - acyl neuraminic acid) is the most widely distributed in nature, mainly of animal cell membranes or secretions, glycoprotein, sugar, lipid or bacteria of capsular material such as sugar. In glycoprotein, or sugar, lipid, the two form the keto group of glycosidic bond and make it located at the end of the side chain of reducing sugar, the negatively charged or unique chemical structure make it .