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  2. Galactose - Wikipedia

    en.wikipedia.org/wiki/Galactose

    Galactose (/ ɡ ə ˈ l æ k t oʊ s /, galacto-+ -ose, "milk sugar"), sometimes abbreviated Gal, is a monosaccharide sugar that is about as sweet as glucose, and about 65% as sweet as sucrose. [2] It is an aldohexose and a C-4 epimer of glucose. [3] A galactose molecule linked with a glucose molecule forms a lactose molecule.

  3. Diastereomer - Wikipedia

    en.wikipedia.org/wiki/Diastereomer

    Glucose and galactose, for instance, are diastereomers. Even though they share the same molar weight, glucose is more stable than galactose. ... Double bond isomers ...

  4. Glucose - Wikipedia

    en.wikipedia.org/wiki/Glucose

    Oligosaccharides of glucose combined with other sugars serve as important energy stores. These include lactose, the predominant sugar in milk, which is a glucose-galactose disaccharide, and sucrose, another disaccharide which is composed of glucose and fructose. Glucose is also added onto certain proteins and lipids in a process called ...

  5. Lactose - Wikipedia

    en.wikipedia.org/wiki/Lactose

    Lactose, or milk sugar, is a disaccharide composed of galactose and glucose and has the molecular formula C 12 H 22 O 11.Lactose makes up around 2–8% of milk (by mass). The name comes from lact (gen. lactis), the Latin word for milk, plus the suffix -ose used to name sugars.

  6. L-Glucose - Wikipedia

    en.wikipedia.org/wiki/L-Glucose

    l-Glucose is an organic compound with formula C 6 H 12 O 6 or O=CH[CH(OH)] 5 H, specifically one of the aldohexose monosaccharides. As the l-isomer of glucose, it is the enantiomer of the more common d-glucose. l-Glucose does not occur naturally in living organisms, but can be synthesized in the laboratory.

  7. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    For example, there are 16 distinct aldohexose stereoisomers, but the name "glucose" means a specific pair of mirror-image aldohexoses. In the Fischer projection, one of the two glucose isomers has the hydroxyl at left on C3, and at right on C4 and C5; while the other isomer has the reversed pattern.

  8. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    Of these D-isomers, all except D-altrose occur in living organisms, but only three are common: D-glucose, D-galactose, and D-mannose. The L-isomers are generally absent in living organisms; however, L-altrose has been isolated from strains of the bacterium Butyrivibrio fibrisolvens. [6]

  9. Xylose isomerase - Wikipedia

    en.wikipedia.org/wiki/Xylose_isomerase

    The most bio-available sugars according to the International Society of Rare Sugars are: glucose, galactose, mannose, fructose, xylose, ribose, and L-arabinose. Twenty hexoses and nine pentoses, including xylulose, were considered to be "rare sugars".