Harman Patil (Editor)

2 Hydroxybutyric acid

Updated on
Share on FacebookTweet on TwitterShare on LinkedInShare on Reddit
Covid-19
Formula  C4H8O3
Molar mass  104.1045 g/mol
2-Hydroxybutyric acid wwwsigmaaldrichcomcontentdamsigmaaldrichstr
Related compounds  erythrose threose 1,2-butanediol 1,3-butanediol 2,3-butanediol 1,4-butanediol

2-Hydroxybutyric acid, also known as alpha-hydroxybutyrate and α-hydroxybutyrate, is a hydroxybutyric acid with the hydroxyl group on the carbon adjacent to the carboxyl. It is a chiral compound having two enantiomers, -2-hydroxybutyric acid and -2-hydroxybutyric acid.

2-Hydroxybutyrate, the conjugate base of 2-hydroxybutyric acid, is produced in mammalian tissues (principally hepatic) that catabolize L-threonine or synthesize glutathione. Oxidative stress or detoxification demands can dramatically increase the rate of hepatic glutathione synthesis. Under such metabolic stress conditions, supplies of L-cysteine for glutathione synthesis become limiting, so homocysteine is diverted from the transmethylation pathway forming methionine into the transsulfuration pathway forming cystathionine. 2-Hydroxybutyrate is released as a byproduct when cystathionine is cleaved to cysteine that is incorporated into glutathione. Chronic shifts in the rate of glutathione synthesis may be reflected by urinary excretion of 2-hydroxybutyrate.

α-hydroxybutyrate may be useful as an early indicator of insulin resistance in non-diabetic subjects. Moreover, elevated serum α-hydroxybutyrate predicts worsening glucose tolerance.

References

2-Hydroxybutyric acid Wikipedia


Similar Topics
Pork Chop Hill
Joël Bourdin
Karl Heinz Radschinsky
Topics
 
B
i
Link
H2
L