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M1134

Sigma-Aldrich

L-(−)-Mannose

≥99% (GC)

Sinônimo(s):

L-Mannopyranose

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About This Item

Fórmula empírica (Notação de Hill):
C6H12O6
Número CAS:
10030-80-5
Peso molecular:
180.16
Beilstein:
1724628
Número CE:
233-080-2
Número MDL:
MFCD00063884
Código UNSPSC:
12352201
ID de substância PubChem:
24896618
NACRES:
NA.25

Ensaio

≥99% (GC)

forma

powder

técnica(s)

gas chromatography (GC): suitable

cor

beige

pf

129-131 °C (lit.)

solubilidade

water: 100 mg/mL, clear, colorless to very faintly yellow

cadeia de caracteres SMILES

OC[C@@H]1OC(O)[C@H](O)[C@H](O)[C@H]1O

InChI

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5+,6?/m0/s1

chave InChI

WQZGKKKJIJFFOK-JFNONXLTSA-N

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Descrição geral

Mannose is a monosaccharide.

Aplicação

L-Mannose has been used in a study to assess substrate specificity of galactokinase from Streptococcus pneumoniae. It has also been used in a study to investigate a versatile route to L-hexoses.

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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Yang Zou et al.
Bioorganic & medicinal chemistry letters, 22(10), 3540-3543 (2012-04-20)
Galactokinases (GalKs) have attracted significant research attention for their potential applications in the enzymatic synthesis of unique sugar phosphates. The galactokinase (GalKSpe4) cloned from Streptococcus pneumoniae TIGR4 presents a remarkably broad substrate range including 14 diverse natural and unnatural sugars.
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In vitro cellular & developmental biology. Plant : journal of the Tissue Culture Association, 50(1), 9-18 (2014-01-01)
Annalisa Guaragna et al.
Organic letters, 8(21), 4863-4866 (2006-10-06)
[reaction: see text] An efficient route for the synthesis of orthogonally protected l-sugars has been opened up, starting from the heterocyclic homologating agent 1 and 2,3-O-isopropylidene-l-glyceraldehyde (2). Our synthetic path enables the synthesis of a 2,3-unsaturated-l-pyranoside, which can be suitably
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Journal of immunology (Baltimore, Md. : 1950), 188(4), 1847-1855 (2012-01-10)
NKG2D ligand surface expression is important for immune recognition of stressed and neotransformed cells. In this study, we show that surface expression of MICA/B and other NKG2D ligands is dependent on N-linked glycosylation. The inhibitor of glycolysis and N-linked glycosylation
Juha P Kotimaa et al.
Journal of immunological methods, 419, 25-34 (2015-03-04)
The complement system is an essential component of our innate immunity, both for the protection against infections and for proper handling of dying cells. However, the complement system can also contribute to tissue injury and inflammatory responses. In view of
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