Use of D-glucose modifications by non-adapted and adapted cell lines was written by Frank, Vladimir;Horakova, Katarina;Valentova, Nadeja;Smelik, Ondrej. And the article was included in Biologia (Bratislava, Slovakia) in 1976.Related Products of 14431-43-7 This article mentions the following:
Three animal cell lines of different origin and different degrees of stabilization (HeLa, LW1, and LWF B55) were cultured in media containing 1 of the following isomers of D-glucose: anhydrous α-D-glucose, β-D-glucose monohydrate, and di-α,β-D-glucose hemihydrate (determined as a racemate). The 3 cell strains exhibited different growth in the 3 different media, and no particular form of glucose was favorable to the growth of all 3 strains, even when the cells were adapted for 7-8 weeks. The cell strains showed different capacities for using the different glucose forms in that they showed different ratios of glucose consumption to growth intensity. Measurements of cell growth, glucose consumption, lactate formation, and glycogen content showed that balanced mixtures of all 3 glucose forms do not lead to identical energy metabolism in the cell cultures used. In the experiment, the researchers used many compounds, for example, (2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate (cas: 14431-43-7Related Products of 14431-43-7).
(2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate (cas: 14431-43-7) belongs to tetrahydropyran derivatives. Tetrahydropyrans are useful synthons for biologically important compounds. The reaction of tertiary 1,4- and 1,5-diols with cerium ammonium nitrate at room temperature gives tetrahydrofuran and tetrahydropyran derivatives in high yield and stereoselectivity. Various fragrant compounds have been synthesized using this method.Related Products of 14431-43-7
Referemce:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics