G9753
α-D-Glucosamine 1-phosphate
Sinônimo(s):
2-Amino-2-deoxy-α-D-glucopyranosyl phosphate
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About This Item
Fórmula empírica (Notação de Hill):
C6H14NO8P
Número CAS:
Peso molecular:
259.15
Número MDL:
Código UNSPSC:
12352201
ID de substância PubChem:
NACRES:
NA.25
Produtos recomendados
fonte biológica
natural (inorganic)
Ensaio
≥97% (TLC)
forma
powder
Impurezas
<8.5% water (Karl Fischer)
cor
white
solubilidade
water: 100 mg/mL, clear, colorless
temperatura de armazenamento
−20°C
cadeia de caracteres 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)
chave InChI
YMJBYRVFGYXULK-UHFFFAOYSA-N
Aplicação
- 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
Outras 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 classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
Certificados de análise (COA)
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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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Journal of the American Chemical Society, 127(6), 1711-1718 (2005-02-11)
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