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M1134

Sigma-Aldrich

L-(−)-Mannose

≥99% (GC)

Sinonimo/i:

L-Mannopyranose

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About This Item

Formula empirica (notazione di Hill):
C6H12O6
Numero CAS:
10030-80-5
Peso molecolare:
180.16
Beilstein:
1724628
Numero CE:
233-080-2
Numero MDL:
MFCD00063884
Codice UNSPSC:
12352201
ID PubChem:
24896618
NACRES:
NA.25

Saggio

≥99% (GC)

Forma fisica

powder

tecniche

gas chromatography (GC): suitable

Colore

beige

Punto di fusione

129-131 °C (lit.)

Solubilità

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

Stringa SMILE

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
WQZGKKKJIJFFOK-JFNONXLTSA-N

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Descrizione generale

Mannose is a monosaccharide.

Applicazioni

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.

Altre note

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (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.
Optimized
Emily Wu et al.
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
Lars Andresen et al.
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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