推荐产品
方案
≥98.0% (TLC)
表单
powder
储存温度
2-8°C
SMILES字符串
OC[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)C(O)=O
InChI
1S/C6H12O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h2-5,7-11H,1H2,(H,12,13)/t2-,3+,4+,5-/m1/s1
InChI key
RGHNJXZEOKUKBD-MGCNEYSASA-N
生化/生理作用
Metabolite in galactose metabolim, non-phosphorylative Entner-Doudoroff pathway, D-galactonate degradation, De Ley-Doudoroff pathway, semi-phosphorylative Entner-Doudoroff pathway
其他说明
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Peter Schadewaldt et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 801(2), 249-255 (2004-01-31)
A stable isotope dilution assay was developed for the sensitive determination of D-galactonic acid. D-[U-13C(6)]galactono-1,4-lactone was prepared as internal standard. Unlabelled and U-13C-labelled D-galactonic acid species were converted to the N-(1-butyl)galactonamide pentaacetate derivatives and assessed by gas chromatography-mass spectrometry (GC-MS).
T Shinka et al.
Journal of chromatography. B, Biomedical sciences and applications, 732(2), 469-477 (1999-10-12)
We determined urinary galactose and 4-hydroxyphenyllactic acid (4HPLA) in 4338 of 5-day-old newborns using a newly developed GC-MS screening method. Fifty-two infants were chemically diagnosed as having transient galactosuria based upon elevated urinary galactose levels (4.78-30.53 mg/mg creatinine, control 1.10
Claire T Yager et al.
Molecular genetics and metabolism, 80(3), 283-289 (2003-12-19)
The red blood cell (RBC) concentration of galactitol and galactonate was measured in 27 patients with galactose-1-phosphate uridyltransferase (GALT) deficiency galactosemia and 19 non-galactosemic subjects by a newly devised isotope dilution gas chromatography/mass spectrometry (GC/MS) method. The method utilizing UL[13C]galactitol
J D Shoemaker et al.
Journal of chromatography, 562(1-2), 125-138 (1991-01-02)
Eighty-five clinical urine samples and nineteen urine samples previously found by other laboratories to suggest genetic metabolic defects were prepared for trimethylsilylation by treatment with urease, followed by azeotropic dehydration. The "Target Analyte Search" program provided with the VG Trio
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