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Merck
CN

M1134

L-(-)-甘露糖

≥99% (GC)

别名:

L-吡喃甘露糖

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关于此项目

经验公式(希尔记法):
C6H12O6
化学文摘社编号:
分子量:
180.16
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
233-080-2
Beilstein/REAXYS Number:
1724628
MDL number:
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产品名称

L-(-)-甘露糖, ≥99% (GC)

InChI key

WQZGKKKJIJFFOK-JFNONXLTSA-N

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

SMILES string

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

assay

≥99% (GC)

form

powder

technique(s)

gas chromatography (GC): suitable

color

beige

mp

129-131 °C (lit.)

solubility

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

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Application

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.

General description

Mannose is a monosaccharide.

Other Notes

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

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

涉药品监管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Pin Guo et al.
Journal of experimental & clinical cancer research : CR, 39(1), 202-202 (2020-10-01)
Globally, colorectal cancer (CRC) affects more than 1 million people each year. In addition to non-modifiable and other environmental risk factors, Fusobacterium nucleatum infection has been linked to CRC recently. In this study, we explored mechanisms underlying the role of
Adriana Navarrete-Solis et al.
Journal of food science and technology, 57(2), 663-672 (2020-03-03)
Spray drying represents a viable alternative for the stabilization of juice and extract of a great diversity of plant in tropical zones, such as jackfruit from Nayarit, Mexico. The jackfruit powder allows physicochemical and microbiological stability for storage, transportation, and
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

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