Uronic acid

For hexuronic acid, i.e. the older name of Vitamin C, see Ascorbic acid.

The β-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 primary alcohol group has been oxidized to a carboxylic acid.

Uronic acids (/jʊˈrɒnᵻk/) are a class of sugar acids with both carbonyl and carboxylic acid functional groups. They are sugars in which the terminal carbon's hydroxyl group 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). Uronic acids that have six carbons are called hexuronic acids.

Examples

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.

External links

• Uronic Acids at the US National Library of Medicine Medical Subject Headings (MeSH)
• Description at zvon.org
• Synthesis at chembio.uoguelph.ca (halfway down page.)