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  2. Haworth projection - Wikipedia

    en.wikipedia.org/wiki/Haworth_projection

    In chemistry, a Haworth projection is a common way of writing a structural formula to represent the cyclic structure of monosaccharides with a simple three-dimensional perspective. Haworth projection approximate the shapes of the actual molecules better for furanoses —which are in reality nearly planar—than for pyranoses that exist in ...

  3. Psicose - Wikipedia

    en.wikipedia.org/wiki/Psicose

    Allulose, also known by its systematic name D-ribo-2-hexulose as well as by the name D-psicose, is a monosaccharide and a ketohexose. [ 2 ] [ 11 ] It is a C3 epimer of fructose . [ 2 ] Fructose can be converted to allulose by the enzymes D -tagatose 3-epimerase ( EC 5.1.3.31 ) and/or D -psicose 3-epimerase ( EC 5.1.3.30 ), which has allowed for ...

  4. N-Acetylglucosamine - Wikipedia

    en.wikipedia.org/wiki/N-Acetylglucosamine

    N-Acetylglucosamine molecule. N-Acetylglucosamine (GlcNAc) is an amide derivative of the monosaccharide glucose.It is a secondary amide between glucosamine and acetic acid.It is significant in several biological systems.

  5. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    The Fischer projection is a systematic way of drawing the skeletal formula of an acyclic monosaccharide so that the handedness of each chiral carbon is well specified. Each stereoisomer of a simple open-chain monosaccharide can be identified by the positions (right or left) in the Fischer diagram of the chiral hydroxyls (the hydroxyls attached ...

  6. Chitin - Wikipedia

    en.wikipedia.org/wiki/Chitin

    Haworth projection of the chitin molecule. A close-up of the wing of a leafhopper ; the wing is composed of chitin. A cicada emerges from its nymphal exoskeleton; the shed exoskeleton is mostly modified chitin ( sclerotin ) but the wings and much of the adult body are still unsclerotized chitin at this stage

  7. Anomer - Wikipedia

    en.wikipedia.org/wiki/Anomer

    2, 3 = Haworth projections. 4 = Mills projection. Every two anomers are designated alpha (α) or beta (β), according to the configurational relationship between the anomeric centre and the anomeric reference atom , hence they are relative stereodescriptors . [ 2 ]

  8. Hexose - Wikipedia

    en.wikipedia.org/wiki/Hexose

    In chemistry, a hexose is a monosaccharide (simple sugar) with six carbon atoms. [1] [2] The chemical formula for all hexoses is C 6 H 12 O 6, and their molecular weight is 180.156 g/mol. [3] Hexoses exist in two forms, open-chain or cyclic, that easily convert into each other in aqueous solutions. [4]

  9. 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.