G9753
α-D-葡萄糖胺 1-磷酸
别名:
2-Amino-2-deoxy-α-D-glucopyranosyl phosphate
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关于此项目
经验公式（希尔记法）:
C6H14NO8P
化学文摘社编号:
分子量:
259.15
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
Quality Level
InChI key
YMJBYRVFGYXULK-UHFFFAOYSA-N
SMILES string
NC1C(O)C(O)C(CO)OC1OP(O)(O)=O
InChI
1S/C6H14NO8P/c7-3-5(10)4(9)2(1-8)14-6(3)15-16(11,12)13/h2-6,8-10H,1,7H2,(H2,11,12,13)
biological source
natural (inorganic)
assay
≥97% (TLC)
form
powder
impurities
<8.5% water (Karl Fischer)
color
white
solubility
water: 100 mg/mL, clear, colorless
storage temp.
−20°C
Application
- 来自热纤梭菌（Ruminiclostridium thermocellum）的纤维糊精磷酸化酶: X-射线晶体结构和底物特异性分析。该研究介绍了利用纤维糊精磷酸化酶进行α-D-葡萄糖胺 1-磷酸类多糖的酶法合成和分析，重点介绍了其在新生物材料开发中的潜力。Field et al., 2017
- 来自梨火疫病菌（Erwinia amylovora）的葡萄糖-1-磷酸尿苷酰转移酶: 活性、结构和底物特异性。该论文探索了细菌代谢中与α-D-葡萄糖胺 1-磷酸相关的生化途径，提供了有关微生物生物化学和抗菌治疗潜在靶点的见解。Field et al., 2017
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)
K Takayama et al.
The Journal of biological chemistry, 258(12), 7379-7385 (1983-06-25)
We have determined the complete structure of a glycolipid (designated lipid X) previously found to accumulate in certain Escherichia coli mutants defective in phosphatidylglycerol synthesis (Nishijima, M., and Raetz, C.R.H. (1979) J. Biol. Chem. 254, 7837-7844). Based on fast atom
F Hatzack et al.
Journal of chromatography. B, Biomedical sciences and applications, 736(1-2), 221-229 (2000-02-17)
A simple and inexpensive high-performance thin-layer chromatography (HPTLC) method for the analysis of inositol mono- to hexakisphosphates on cellulose precoated plates is described. Plates were developed in 1-propanol-25% ammonia solution-water (5:4:1) and substance quantities as low as 100-200 pmol were
E V Vorob'eva et al.
Bioorganicheskaia khimiia, 32(5), 538-545 (2006-10-18)
The hydrolysis of defatted cells of the marine bacterium Chryseobacterium scophtalmum CIP 104199T with 10% acetic acid (3 h, 100 degrees C) led to an unusual lipid A (LA) (yield 0.6%), obtained for the first time. Using chemical analysis, FAB
Seema C Namboori et al.
Journal of bacteriology, 190(8), 2987-2996 (2008-02-12)
Archaea and eukaryotes share a dolichol phosphate-dependent system for protein N-glycosylation. In both domains, the acetamido sugar N-acetylglucosamine (GlcNAc) forms part of the core oligosaccharide. However, the archaeal Methanococcales produce GlcNAc using the bacterial biosynthetic pathway. Key enzymes in this
S Ambrosio et al.
Journal of biochemical and biophysical methods, 25(4), 237-244 (1992-12-01)
Galactosamine is quickly metabolized to galactosamine 1-phosphate in rats treated with this compound. An HPLC method to quantify hexosamine phosphates in biological samples is described, modified from the o-phthaldialdehyde amino acid analysis procedure. o-Phthaldialdehyde derivatives of hexosamines and hexosamine-phosphates can
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