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aldohexose's Usage Examples:

glucose, can exist as a linear (carboxo-)aldohexose (<1%), or as a cyclic hemiacetal (furanose or pyranose).

For instance, galactose and glucose are both aldohexoses, but have different physical structures and chemical properties.

As an example, four of the carbon atoms of the aldohexose class of molecules are asymmetric, therefore the Le Bel–Van "t Hoff rule.

This change has the same effect on the other aldohexoses, as well.

nicotinamide adenine dinucleotide phosphate-linked aldohexose, dehydrogenase, NADP+-linked aldohexose dehydrogenase, NADP+-dependent glucose dehydrogenase.

Mannose is a sugar monomer of the aldohexose series of carbohydrates.

In linear form, an aldohexose has four chiral centres, which give 16 possible aldohexose stereoisomers (24),comprising 8 pairs of.

compound with formula C6H12O6 or OCH[CH(OH)]5H, specifically one of the aldohexose monosaccharides.

It is an aldohexose and a C-4 epimer of glucose.

containing six carbon atoms and an aldehyde group, and is therefore an aldohexose.

names in common use include aldose dehydrogenase, and dehydrogenase, D-aldohexose.

aldopentose with 3 asymmetric carbon atoms has 23 8 stereoisomers: An aldohexose with 4 asymmetric carbon atoms has 24 16 stereoisomers: The four groups.

For example, glucose is an aldohexose (a six-carbon aldehyde), ribose is an aldopentose (a five-carbon aldehyde).