G9753
α-D-Glucosamine 1-phosphate
Sinónimos:
2-Amino-2-deoxy-α-D-glucopyranosyl phosphate
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About This Item
Fórmula empírica (notación de Hill):
C6H14NO8P
Número de CAS:
Peso molecular:
259.15
Número MDL:
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
NACRES:
NA.25
Productos recomendados
origen biológico
natural (inorganic)
Nivel de calidad
Ensayo
≥97% (TLC)
Formulario
powder
impurezas
<8.5% water (Karl Fischer)
color
white
solubilidad
water: 100 mg/mL, clear, colorless
temp. de almacenamiento
−20°C
cadena SMILES
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)
Clave InChI
YMJBYRVFGYXULK-UHFFFAOYSA-N
Categorías relacionadas
Aplicación
- Cellodextrin phosphorylase from Ruminiclostridium thermocellum: X-ray crystal structure and substrate specificity analysis. This study presents the enzymatic synthesis and analysis of alpha-ᴅ-Glucosamine 1-phosphate based polysaccharides using cellodextrin phosphorylase, showcasing potential for novel biomaterial development. Field et al., 2017
- Glucose-1-phosphate uridylyltransferase from Erwinia amylovora: Activity, structure and substrate specificity. This paper explores the biochemical pathway involving alpha-ᴅ-Glucosamine 1-phosphate in the context of bacterial metabolism, providing insights into microbial biochemistry and potential targets for antibacterial therapy. Field et al., 2017
Otras notas
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Equipo de protección personal
Eyeshields, Gloves, type N95 (US)
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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
Fumitaka Kudo et al.
Journal of the American Chemical Society, 127(6), 1711-1718 (2005-02-11)
Aminoglycoside antibiotics are composed of aminosugars and a unique aminocyclitol aglycon including 2-deoxystreptamine (DOS), streptidine, actinamine, etc., and nucleotidylyltransferases, sugar modifying enzymes, and glycosyltransferases appear to be essential for their biosynthesis. However, the genes encoding those enzymes were unable to
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
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
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
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