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Merck
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Key Documents

추가 자료

M1134

Sigma-Aldrich

L-(−)-Mannose

≥99% (GC)

동의어(들):

L-Mannopyranose

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About This Item

실험식(Hill 표기법):
C6H12O6
CAS Number:
10030-80-5
Molecular Weight:
180.16
Beilstein:
1724628
EC Number:
233-080-2
MDL number:
MFCD00063884
UNSPSC 코드:
12352201
PubChem Substance ID:
24896618
NACRES:
NA.25

분석

≥99% (GC)

형태

powder

기술

gas chromatography (GC): suitable

색상

beige

mp

129-131 °C (lit.)

solubility

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

SMILES string

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

InChI key

WQZGKKKJIJFFOK-JFNONXLTSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

일반 설명

Mannose is a monosaccharide.

애플리케이션

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.

기타 정보

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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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