When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Monosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide_nomenclature

    Another nomenclature uses the systematic name of the molecular graph, a ' D-' or ' L-' prefix to indicate the position of the last chiral hydroxyl on the Fischer diagram (as above), and another italic prefix to indicate the positions of the remaining hydroxyls relative to the first one, read from bottom to top in the diagram, skipping the keto ...

  3. Monosaccharide - Wikipedia

    en.wikipedia.org/wiki/Monosaccharide

    These specific monosaccharide names have conventional three-letter abbreviations, like "Glu" for glucose and "Thr" for threose. Generally, a monosaccharide with n asymmetrical carbons has 2 n stereoisomers. The number of open chain stereoisomers for an aldose monosaccharide is larger by one than that of a ketose monosaccharide of the same length.

  4. Template:Biography - Wikipedia

    en.wikipedia.org/wiki/Template:Biography

    Wikipedia is not a soapbox for individuals to espouse their views. However, views held by politicians, writers, and others may be summarized in their biography only to the extent those views are covered by reliable sources that are independent of the control of the politician, writer, etc.

  5. Symbol Nomenclature For Glycans - Wikipedia

    en.wikipedia.org/wiki/Symbol_Nomenclature_For...

    Monosaccharide color code in the Symbol Nomenclature For Glycans (SNFG) The Symbol Nomenclature For Glycans ( SNFG ) [ 1 ] is a community-curated standard for the depiction of simple monosaccharides and complex carbohydrates ( glycans ) using various colored-coded, geometric shapes, along with defined text additions.

  6. Oligosaccharide nomenclature - Wikipedia

    en.wikipedia.org/wiki/Oligosaccharide_nomenclature

    An oligosaccharide has both a reducing and a non-reducing end. The reducing end of an oligosaccharide is the monosaccharide residue with hemiacetal functionality, thereby capable of reducing the Tollens’ reagent, while the non-reducing end is the monosaccharide residue in acetal form, thus incapable of reducing the Tollens’ reagent. [2]

  7. Category:Monosaccharides - Wikipedia

    en.wikipedia.org/wiki/Category:Monosaccharides

    Monosaccharides are carbohydrates in the form of simple sugars. Like disaccharides , they are sweet, water soluble and crystalline . The main article for this category is Monosaccharides .

  8. Nucleotide sugar - Wikipedia

    en.wikipedia.org/wiki/Nucleotide_sugar

    Cytidine Diphosphate: CDP-D-Ribitol (i.e. CMP-[ribitol phosphate]); [8] though not a sugar, the phosphorylated sugar alcohol ribitol phosphate is incorporated into matriglycan as if it were a monosaccharide. In other forms of life many other sugars are used and various donors are utilized for them.

  9. Category:Carbohydrate chemistry - Wikipedia

    en.wikipedia.org/wiki/Category:Carbohydrate...

    Carbohydrate chemistry is a field of study concerned with the synthesis, structure and function of carbohydrates.Due to the complexity of these structures, the chemical synthesis of carbohydrates has a variety of unique strategies and methods.