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  2. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    The number of open chain stereoisomers for an aldose monosaccharide is larger by one than that of a ketose monosaccharide of the same length. Every ketose will have 2 (n−3) stereoisomers where n > 2 is the number of carbons. Every aldose will have 2 (n−2) stereoisomers where n > 2 is the number of carbons. These are also referred to as ...

  3. Monosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide_nomenclature

    Note that, in this nomenclature, mirror-image isomers differ only in the ' D '/' L ' prefix, even though all their hydroxyls are reversed. The following tables shows the Fischer projections of selected monosaccharides (in open-chain form), with their conventional names. The table shows all aldoses with 3 to 6 carbon atoms, and a few ketoses.

  4. Carbohydrate - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate

    A carbohydrate is a biomolecule consisting of carbon (C), hydrogen (H) and oxygen (O) atoms, usually with a hydrogen–oxygen atom ratio of 2:1 (as in water) and thus with the empirical formula C m (H 2 O) n (where m may or may not be different from n), which does not mean the H has covalent bonds with O (for example with CH 2 O, H has a covalent bond with C but not with O).

  5. L-Glucose - Wikipedia

    en.wikipedia.org/wiki/L-Glucose

    [2] Like the d-isomer, l-glucose usually occurs as one of four cyclic structural isomers—α- and β-l-glucopyranose (the most common, with a six-atom ring), and α- and β-l-glucofuranose (with a five-atom ring). In water solution, these isomers interconvert in matters of hours, with the open-chain form as an intermediate stage.

  6. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    In general, only one of the two enantiomers occurs naturally (for example, D-glucose) and can be metabolized by animals or fermented by yeasts. The term "hexose" sometimes is assumed to include deoxyhexoses , such as fucose and rhamnose : compounds with general formula C 6 H 12 O 6− y that can be described as derived from hexoses by ...

  7. Triose - Wikipedia

    en.wikipedia.org/wiki/Triose

    [2] Importance of Triose in the Body Trioses serve as metabolic intermediates in various different metabolic pathways such as glycolysis, gluconeogenesis, and the pentose phosphate pathway. Trioses contribute to the synthesis of essential biomolecules including lipids, amino acids, nucleotides, and carbohydrates.

  8. Glycome - Wikipedia

    en.wikipedia.org/wiki/Glycome

    Carbohydrates consist of "hydrated carbon", i.e. [CH 2 O]n. Monosaccharides are a carbohydrate that cannot be hydrolyzed into a simpler carbohydrate and are the building blocks of oligosaccharides and polysaccharides. Oligosaccharides are linear or branched chains of monosaccharides attached to one another via glycosidic linkages. The number of ...

  9. Isomer - Wikipedia

    en.wikipedia.org/wiki/Isomer

    For example, replacing two atoms of common hydrogen by deuterium (, or ) on an ethane molecule yields two distinct structural isomers, depending on whether the substitutions are both on the same carbon (1,1-dideuteroethane, ) or one on each carbon (1,2-dideuteroethane, ); as if the substituent was chlorine instead of deuterium.