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F8150

Sigma-Aldrich

D-(+)-Fucose

≥97% (GC)

Sinônimo(s):

6-Deoxy-D-galactose, Rhodeose

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About This Item

Fórmula empírica (Notação de Hill):
C6H12O5
Número CAS:
3615-37-0
Peso molecular:
164.16
Beilstein:
1723320
Número CE:
222-792-9
Número MDL:
MFCD00135603
Código UNSPSC:
12352201
ID de substância PubChem:
24894959
NACRES:
NA.25

fonte biológica

synthetic

Ensaio

≥97% (GC)

forma

powder

atividade óptica

[α]20/D 74 to 76 °, c = 4% (w/v) in water

técnica(s)

gas chromatography (GC): suitable

cor

white

pf

144-145 °C (lit.)

solubilidade

H2O: 100 mg/mL, clear to slightly hazy, colorless to faintly yellow

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

C[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)C=O

InChI

1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4+,5+,6-/m1/s1

chave InChI

PNNNRSAQSRJVSB-DPYQTVNSSA-N

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Categorias relacionadas

Aplicação

D-Fucose (6-deoxy-D-galactose, rhodeose) may be used to study enzymes involved in its mutarotation to form L-fucose. It may be used as a reference compound in the analysis of carbohydrate metabolites. D-Fucose may be used to study biological processes such as adhesion.

Ações bioquímicas/fisiológicas

D-Fucose is a nonmetabolizable analog of L-Arabinose.

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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Zhenzheng Hu et al.
Structure (London, England : 1993), 26(1), 60-71 (2017-12-12)
Mannose receptor (MR, CD206) is an endocytic receptor on microphages and dendritic cells. It recognizes multiple ligands and plays important roles in regulating immune responses and maintaining glycoprotein homeostasis. However, the structure and functional mechanism of MR remain unclear. Here we
P Wlodarczyk et al.
Journal of physics. Condensed matter : an Institute of Physics journal, 25(37), 375101-375101 (2013-08-15)
The sugar specific mutarotation reaction in biologically important L-fucose and its enantiomer in the pure, anhydrous, supercooled liquid state has been studied. Kinetics measurements in the temperature range 313-328 K at ambient pressure have been performed by means of dielectric spectroscopy
Nancy G Isern et al.
Biotechnology for biofuels, 6(1), 47-47 (2013-04-05)
Caldicellulosiruptor saccharolyticus is a thermophilic, Gram-positive, non-spore forming, strictly anaerobic bacterium of interest in potential industrial applications, including the production of biofuels such as hydrogen or ethanol from lignocellulosic biomass through fermentation. High-resolution, solution-state nuclear magnetic resonance (NMR) spectroscopy is
Sarah Meinhardt et al.
Nucleic acids research, 40(21), 11139-11154 (2012-09-12)
LacI/GalR transcription regulators have extensive, non-conserved interfaces between their regulatory domains and the 18 amino acids that serve as 'linkers' to their DNA-binding domains. These non-conserved interfaces might contribute to functional differences between paralogs. Previously, two chimeras created by domain
Xiaonan Zhou et al.
PloS one, 13(10), e0204152-e0204152 (2018-10-09)
Lonicera japonica is a typical Chinese herbal medicine. We previously reported a method to isolate polysaccharides from Lonicera japonica (LJP). In this study, we first performed a qualitative analysis of LJP using the Fourier Transform Infrared Spectrometer (FT-IR) and explored
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