Noun
a sweet crystalline aldehyde formed by the breakdown of sugars
Source: WordNetChirality nomenclature Like many chiral molecules, the two stereoisomers of glyceraldehyde will gradually rotate the polarization direction of linearly polarized light as it passes through it, even in solution. Source: Internet
Figure 6: Metabolic conversion of fructose to glycogen in the liver Synthesis of triglyceride from DHAP and glyceraldehyde 3-phosphate Carbons from dietary fructose are found in both the free fatty acid and glycerol moieties of plasma triglycerides. Source: Internet
It indicates that the C-2 chiral center has the same handedness as that of D -glyceraldehyde (which was so labeled because it is dextrorotatory). Source: Internet
Most (5 out of 6 molecules) of the glyceraldehyde 3-phosphate produced is used to regenerate ribulose 1,5-bisphosphate so the process can continue. Source: Internet
One of the steps in this sequence allows the isolation of enantiopure ribose aminooxazoline if the enantiomeric excess of glyceraldehyde is 60% or greater, of possible interest towards biological homochirality. Source: Internet
Synthesis of glycogen from DHAP and glyceraldehyde 3-phosphate The resultant glyceraldehyde formed by aldolase B then undergoes phosphorylation to glyceraldehyde 3-phosphate. Source: Internet