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Key Documents

Outros documentos

G7134

Sigma-Aldrich

L-(−)-Galactose

≥99% (HPLC)

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About This Item

Fórmula empírica (Notação de Hill):
C6H12O6
Número CAS:
15572-79-9
Peso molecular:
180.16
Beilstein:
1724622
Número CE:
239-630-8
Número MDL:
MFCD00063833
Código UNSPSC:
12352201
ID de substância PubChem:
24895293

Nível de qualidade

100

Ensaio

≥99% (HPLC)

forma

powder

técnica(s)

HPLC: suitable

cor

white

solubilidade

water: 50 mg/mL, clear, colorless

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-DHVFOXMCSA-N

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Categorias relacionadas

Ações bioquímicas/fisiológicas

L-Galactose was shown to be a key intermediate in the molecular pathway of converting D-glucose to oxalic acid in Pistia stratiotes.

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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Sigma-Aldrich

220477

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D-(+)-Galactose ≥99% (HPLC), BioReagent, suitable for cell culture, suitable for insect cell culture

Sigma-Aldrich

G5388

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L-(−)-Fucose analytical standard

Supelco

93183

L-(−)-Fucose

D-(+)-Fucose ≥98% (GC)

Sigma-Aldrich

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D-(+)-Fucose

Minoru Tomizawa et al.
Oncology letters, 14(1), 899-902 (2017-07-12)
Tissues surrounding hepatocellular carcinomas (HCCs) lack glucose. Hepatocyte selection medium (HSM) is deficient in glucose and is supplemented with galactose. HCC cells were cultured in HSM to investigate the stem cell markers α-fetoprotein (AFP) and cluster of differentiation 44 (CD44).
Patrick Hossler et al.
mAbs, 9(4), 715-734 (2017-04-05)
Protein glycosylation is arguably the paramount post-translational modification on recombinant glycoproteins, and highly cited in the literature for affecting the physiochemical properties and the efficacy of recombinant glycoprotein therapeutics. Glycosylation of human immunoglobulins follows a reasonably well-understood metabolic pathway, which
S E Keates et al.
Phytochemistry, 53(4), 433-440 (2000-03-24)
Axenic Pistia stratiotes L. plants were pulse-chase labeled with [14C]oxalic acid, L[1-14C]ascorbic acid, L-6-14C]ascorbic acid, D-[1-14C]erythorbic acid, L-[1-14C]galactose, or [1-14C]glycolate. Specific radioactivities of L-ascorbic acid (AsA), free oxalic acid (OxA) and calcium oxalate (CaOx) in labeled plants were compared. Samples
Mili Thakur et al.
Scientific reports, 7(1), 231-231 (2017-03-24)
Premature ovarian insufficiency (POI) is a frequent long-term complication of classic galactosemia. The majority of women with this disorder develop POI, however rare spontaneous pregnancies have been reported. Here, we evaluate the effect of D-galactose and its metabolites, galactitol and
Dimitri Daudu et al.
Frontiers in plant science, 8, 1614-1614 (2017-10-06)
Cytokinin signaling is a key regulatory pathway of many aspects in plant development and environmental stresses. Herein, we initiated the identification and functional characterization of the five CHASE-containing histidine kinases (CHK) in the economically important
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