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  2. Ribose - Wikipedia

    en.wikipedia.org/wiki/Ribose

    L-Ribose Fischer Projection. Ribose is a simple sugar and carbohydrate with molecular formula C 5 H 10 O 5 and the linear-form composition H−(C=O)−(CHOH) 4 −H. The naturally occurring form, d-ribose, is a component of the ribonucleotides from which RNA is built, and so this compound is necessary for coding, decoding, regulation and expression of genes.

  3. Adenylosuccinate lyase deficiency - Wikipedia

    en.wikipedia.org/wiki/Adenylosuccinate_lyase...

    D-ribose and uridine administration [5] ... The second is the buildup of accumulating succinylpurines causes neurotoxic effects. In the severely affected individuals, ...

  4. D-Ribose pyranase - Wikipedia

    en.wikipedia.org/wiki/D-Ribose_Pyranase

    D-Ribose pyranase is an enzyme that catalyzes the interconversion of β-D-ribopyranose and β-D-ribofuranose. [1] This enzyme is an isomerase that has only been found in bacteria and viruses . It has two known functions of helping transport ribose into cells and producing β- D -ribofuranose, which can later be used to make ribose 5-phosphate ...

  5. Adenosine monophosphate deaminase deficiency type 1

    en.wikipedia.org/wiki/Adenosine_monophosphate...

    Symptomatic relief from the effects of MADD may sometimes be achieved by administering ribose orally at a dose of approximately 10 grams per 100 pounds (0.2 g/kg) of body weight per day, and exercise modulation as appropriate. Taken hourly, ribose provides a direct but limited source of energy for the cells.

  6. Carbohydrate acetalisation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_acetalisation

    D-ribose in itself is a hemiacetal and in equilibrium with the pyranose 3. In aqueous solution ribose is 75% pyranose and 25% furanose and a different acetal 4 is formed. Selective acetalization of carbohydrate and formation of acetals possessing atypical properties is achieved by using arylsulfonyl acetals.

  7. Deoxyribose - Wikipedia

    en.wikipedia.org/wiki/Deoxyribose

    The term "2-deoxyribose" may refer to either of two enantiomers: the biologically important d-2-deoxyribose and to the rarely encountered mirror image l-2-deoxyribose. [3] d-2-deoxyribose is a precursor to the nucleic acid DNA. 2-deoxyribose is an aldopentose, that is, a monosaccharide with five carbon atoms and having an aldehyde functional group.