Lyxose is an aldopentose — a monosaccharide containing five carbon atoms, and including an aldehyde functional group. It has chemical formula C 5 H 10 O 5. It is a C'-2 carbon epimer of the sugar xylose. The name "lyxose" comes from reversing the prefix "xyl" in "xylose".

D-Lyxose | C5H10O5 | CID 439240 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Lyxose is a ketopentose form that can be obtained from the epimerization of d-xylose, as suggested in the Anet mechanism. AI generated definition based on: Carbohydrate Research, 2015

Aldehydo-D-lyxose is a D-lyxose in open-chain aldehyde form. It is an enantiomer of an aldehydo-L-lyxose. (2S,3S,4R)-2,3,4,5-tetrahydroxypentanal has been reported in Arabidopsis thaliana and Pogostemon cablin with data available. See also: D-Lyxose (annotation moved to); GlyTouCan:G88438YV (annotation moved to). -2.3. 150.05282342 Da. 98 Ų. 104.

The meaning of LYXOSE is a crystalline aldose sugar C5H10O5 that is the epimer of xylose.

Lyxose is a monosaccharide, specifically an aldose, that is one of the less common naturally occurring sugars. It is a C-3 epimer of ribose, meaning it has the same molecular formula but a different spatial arrangement of the hydroxyl groups around the third carbon atom.

Colloids are generally classified into two systems, reversible and irreversible. In a reversible system the products of a physical or chemical reaction may be induced to interact so as to reproduce the original components.

Jan 27, 2025 · D-Lyxose is a C’-2 epimer of D-Xylose (X750750). It is a monosaccharide and a reducing carbohydrate present in maple syrup. It is used in molecular modeling calculations in the study of drug binding and recognition in relation to aldose reductase.

For example, reduction of D-glucose and D-gulose lead to D- and L-glucitol, respectively. However, glucitol enantiomers are not separated on regular chromatographic columns. Another example is that of D-arabinose and D-lyxose, which both generate D-arabitol.

Apr 10, 2025 · Aldopentoses have three chirality centers and a total of 2 3 = 8 possible stereoisomers, or four D, L pairs of enantiomers. These four pairs are called ribose, arabinose, xylose, and lyxose. All except lyxose occur widely in nature.