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TRS testicular regression syndrome; total reducing sugars; tubuloreticular structure
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sugars Those carbohydrates (saccharides) having the general composition (CH2O)n and simple derivatives thereof. Although the simple monomeric sugars (glycoses) are often written as polyhydroxy aldehydes or ketones, e.g., HOCH2-(CHOH)4-CHO for aldohexoses (e.g., glucose) or HOCH2-(CHOH)3-CO-CH2OH for 2-ketoses (e.g., fructose), cyclization can give rise to varied structures as described below. Sugars are generally identifiable by the ending -ose or, if in combination with a nonsugar (aglycon), -oside or -osyl. Sugars especially d-glucose, are the chief source of energy, by oxidation, in nature, and they and their derivatives (e.g., d-glucosamine, d-glucuronic acid), in polymeric form, are major constituents of mucoproteins, bacterial cell walls, and plant structural material (e.g., cellulose). Sugars are often found in combination with steroids (steroid glycosides) and other aglycons.
(05 Mar 2000)
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adenosine diphosphate sugars Esters formed between the aldehydic carbon of sugars and the terminal phosphate of adenosine diphosphate.
(12 Dec 1998)
amino sugars Sugar's in which a hydroxyl group has been replaced with an amino group; e.g., d-glucosamine.
(05 Mar 2000)
guanosine diphosphate sugars Esters formed between the aldehydic carbon of sugars and the terminal phosphate of guanosine diphosphate.
(12 Dec 1998)
polyisoprenyl phosphate sugars Compounds functioning as activated glycosyl carriers in the biosynthesis of glycoproteins and glycophospholipids. They include the polyisoprenyl pyrophosphates.
(12 Dec 1998)
nucleoside-diphosphate sugars Nucleoside diphosphates linked through the 5'-diphosphoric group with simple or complex carbohydrates; e.g., GDP-mannose, UDP-glucose (UDPG), dTDP-glucosamine.
(05 Mar 2000)
dTDP-sugars Sugars or sugar derivatives bonded to dTDP.
(05 Mar 2000)
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