The α-D form of glucuronic acid (after oxidization).

Glucose (before oxidization. Note difference at "6".)

The Fischer projections of glucose and glucuronic acid. Glucose's terminal carbon's hydroxyl group has been oxidized to a carboxylic acid.

A uronic acid is a sugar acid with both a carbonyl and a carboxylic acid function. It is best thought of as a sugar in which the terminal carbon's hydroxyl function has been oxidized to a carboxylic acid. (Oxidation of the terminal aldehyde instead yields an aldonic acid while oxidation of both the terminal hydroxyl group and the aldehyde yields an aldaric acid.) The names of uronic acids are generally based on their parent sugars, however some of the most common do not have direct parents, and are formed by epimerization (e.g iduronic acid is an epimer of glucuronic acid) . Some of these compounds have important biochemical functions; for example, many wastes in the human body are excreted in the urine as their glucuronate salts, and iduronic acid is a component of some structural complexes such as proteoglycans.

[edit] External links

• MeSH Uronic+Acids
• Description at zvon.org
• Synthesis at chembio.uoguelph.ca (halfway down page.)

This article about an organic compound is a stub. You can help Wikipedia by expanding it. v • d • e