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经验公式(希尔记法):
C8H15NO6
化学文摘社编号:
分子量:
221.21
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
231-368-2
Beilstein/REAXYS Number:
1727589
MDL number:
产品名称
N -乙酰基- D -氨基葡萄糖, ≥99% (HPLC)
InChI key
OVRNDRQMDRJTHS-RTRLPJTCSA-N
InChI
1S/C8H15NO6/c1-3(11)9-5-7(13)6(12)4(2-10)15-8(5)14/h4-8,10,12-14H,2H2,1H3,(H,9,11)/t4-,5-,6-,7-,8?/m1/s1
SMILES string
CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O
biological source
crab (red)
assay
≥99% (HPLC)
form
powder
technique(s)
HPLC: suitable
color
white to off-white
mp
211 °C (dec.) (lit.)
solubility
H2O: 50 mg/mL, clear to very slightly hazy (colorless to faint yellow solution)
storage temp.
−20°C
Quality Level
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Application
N-乙酰-D-葡萄糖胺已用于:
- 用作凝集素组织化学竞争性抑制糖
- 用作培养伯氏疏螺旋体螺旋体菌(Borrelia burgdorferi spirochetes)株的 Barbour-Stonner-Kelly (BSK) 培养基成分
- 用作重悬肺炎链球菌(Streptococcus pneumoniae)菌株的结合缓冲液成分,以便通过抑制测定检验M-ficolin纤维胶凝蛋白与肺炎链球菌(S. pneumoniae )菌株结合的特异性
Biochem/physiol Actions
N-乙酰葡糖胺(GlcNAc)主要用于食品、化妆品和制药行业。
General description
N-乙酰葡糖胺(GlcNAc)是葡糖胺(GlcN)的乙酰化衍生物。它是蛋白聚糖、糖蛋白、糖胺聚糖(GAG)和结缔组织中的其他合成单体的重要成分。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Kwang-Hyup Lee et al.
Tissue & cell, 48(4), 361-369 (2016-05-29)
The morphological characteristics and glycoconjugate composition of the vomeronasal organ (VNO) of the horse was investigated using histological, immunohistochemical, and lectin histochemical methods. The VNO is bilaterally located at the base of the nasal septum, has a tubular structure surrounded
Bingwu Yu et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 228, 159-165 (2013-01-09)
Strong (1)H-(1)H coupling can significantly reduce the accuracy of (1)J(CH) measured from frequency differences in coupled HSQC spectra. Although accurate (1)J(CH) values can be extracted from spectral simulation, it would be more convenient if the same accurate (1)J(CH) values can
Yasuhito Onodera et al.
The Journal of clinical investigation, 124(1), 367-384 (2013-12-10)
There is a considerable resurgence of interest in the role of aerobic glycolysis in cancer; however, increased glycolysis is frequently viewed as a consequence of oncogenic events that drive malignant cell growth and survival. Here we provide evidence that increased
Lucy G Weaver et al.
Carbohydrate research, 371, 68-76 (2013-03-26)
Poly-N-acetylglucosamine (PNAG) saccharides are an important constituent of bacterial biofilms, such as those produced by Staphylococcus aureus. We have developed a simple two-step iterative method for the synthesis of β-(1→6)-glucosamine oligosaccharides that are structurally similar to PNAG. We illustrate the
Colette Cywes-Bentley et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(24), E2209-E2218 (2013-05-30)
Microbial capsular antigens are effective vaccines but are chemically and immunologically diverse, resulting in a major barrier to their use against multiple pathogens. A β-(1→6)-linked poly-N-acetyl-d-glucosamine (PNAG) surface capsule is synthesized by four proteins encoded in genetic loci designated intercellular
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