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Keto acid

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In organic chemistry, keto acids or ketoacids (also called oxo acids or oxoacids) are that contain a group () and a group ().Franz Dietrich Klingler, Wolfgang Ebertz "Oxocarboxylic Acids" in Ullmann's Encyclopedia of Industrial Chemistry 2005, Wiley-VCH, Weinheim. In several cases, the keto group is hydrated. The alpha-keto acids are especially important in biology as they are involved in the Krebs citric acid cycle and in .Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. .

Common types of keto acids include:

  • Alpha-keto acids, alpha-ketoacids, or 2-oxoacids have the keto group adjacent to the carboxylic acid. They often arise by oxidative deamination of , and reciprocally, they are precursors to the same. Alpha-keto acids possesses extensive chemistry as agents. Furthermore, alpha-keto acids such as phenylpyruvic acid are endogenous sources for (as a gasotransmitter) and pharmaceutical prodrug scaffold. Important representatives:
  • Beta-keto acids, beta-ketoacids, or 3-oxoacids, such as , have the ketone group at the second carbon from the carboxylic acid. They generally form by the Claisen condensation. The presence of the keto group at the beta position allows them to easily undergo thermal .
  • Gamma-keto acids, Gamma-ketoacids, or 4-oxoacids have the ketone group at the third carbon from the carboxylic acid. is an example.

Keto acids appear in a wide variety of anabolic pathways in metabolism. For instance, in plants (specifically, in , , and fool's parsley), 5-oxo-octanoic acid is converted in enzymatic and non-enzymatic steps into the class of .

When ingested and levels are low, stored fats and proteins are the primary source of energy production. Glucogenic amino acids from proteins and/or from are converted to . Ketogenic amino acids can be deaminated to produce alpha keto acids and .

Alpha keto acids are used primarily as energy for liver cells and in fatty acid synthesis, also in the liver.


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