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Merck
CN

649694

Sigma-Aldrich

N-乙酰-D-神经氨酸-1,2,3-13C3

≥99 atom % 13C, ≥97% (CP)

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别名:
唾液酸-13C3
经验公式(希尔记法):
13C3C8H19NO9
分子量:
312.25
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.12

同位素纯度

≥99 atom % 13C

质量水平

检测方案

≥97% (CP)

mp

186 °C (lit.)

质量偏移

M+3

储存温度

−20°C

SMILES字符串

CC(=O)N[C@@H]1[C@@H](O)[13CH2][13C](O)(O[C@H]1[C@H](O)[C@H](O)CO)[13C](O)=O

InChI

1S/C11H19NO9/c1-4(14)12-7-5(15)2-11(20,10(18)19)21-9(7)8(17)6(16)3-13/h5-9,13,15-17,20H,2-3H2,1H3,(H,12,14)(H,18,19)/t5-,6+,7+,8+,9+,11?/m0/s1/i2+1,10+1,11+1

InChI key

SQVRNKJHWKZAKO-JQVNYIDJSA-N

一般描述

N-乙酰基-D-神经氨酸-1,2,3-13C3 是N-乙酰基-D-神经氨酸的同位素。

应用

N-乙酰基-D-神经氨酸-1,2,3-13C3 可用于通过13C NMR波谱仪定量测定无环酮、酮水合物和烯醇。它也可用于测定作为NANS缺陷患者治疗途径的唾液酸增补剂。

包装

该产品可以大包装形式供货,也可按需进行包装。 如需关于价格、供货形式及包装的信息,请联系稳定同位素客户服务

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Sialin, encoded by the SLC17A5 gene, is a lysosomal sialic acid transporter defective in Salla disease, a rare inherited leukodystrophy. It also enables metabolic incorporation of exogenous sialic acids, leading to autoantibodies against N-glycolylneuraminic acid in humans. Here, we identified
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Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology, 238, 110336-110336 (2019-09-03)
Understanding variation in physiological traits across taxa is a central question in evolutionary biology that has wide-ranging implications in biomedicine, disease ecology, and environmental protection. Sialic acid (Sia), and in particular, 5-N-acetylneuraminic acid (Neu5Ac), is chemically bound to galactose and
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Aqueous solutions of N-acetyl-neuraminic acid (Neu5Ac, 1) labeled with (13)C at C1, C2, and/or C3 were analyzed by (13)C NMR spectroscopy to detect and quantify the acyclic forms (keto, keto hydrate, enol) present at varying pHs. In addition to pyranoses
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In NANS deficiency, biallelic mutations in the N-acetylneuraminic acid synthase (NANS) gene impair the endogenous synthesis of sialic acid (N-acetylneuraminic acid) leading to accumulation of the precursor, N-acetyl mannosamine (ManNAc), and to a multisystemic disorder with intellectual disability. The aim

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