3-Aminoisobutyric acid
Product of thymine metabolism
From Wikipedia, the free encyclopedia
3-Aminoisobutyric acid (also known as β-aminoisobutyric acid or BAIBA) is a product formed by the catabolism of thymine and valine.[1]
| Names | |
|---|---|
| Preferred IUPAC name
3-Amino-2-methylpropanoic acid | |
| Other names
3-Aminoisobutyrate | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.005.132 |
| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C4H9NO2 | |
| Molar mass | 103.12 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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During exercise, the increase of PGC-1α protein triggers the secretion of BAIBA from exercising muscles into the blood (concentration 2 to 3 μM in human serum). When BAIBA reaches white fat tissue, it activates the expression of thermogenic genes via PPARα receptors, resulting in browning of white fat cells.[2] One of the consequences of BAIBA activity is increased background metabolism of BAIBA target cells.
BAIBA is thought to play a number of roles in cell metabolism, regulation of fat burning, and regulation of insulin, blood triglycerides, and total cholesterol.[3][4][5]
BAIBA is found as a normal metabolite of skeletal muscle (myokine). Its plasma concentrations are increased by exercise.[6] The increased production is likely a result of enhanced mitochondrial activity,[7] as this increase is also observed in muscle of PGC-1a overexpression mice. BAIBA is a proposed protective factor against metabolic disorders since it can induce brown fat function.[2] But healthy diet with exercise is better.[8][9][6][10][11][12]
See also
- β-Alanine
- beta-Hydroxy beta-methylbutyric acid (HMB) – Chemical compound
- GABA – Main inhibitory neurotransmitter in the mammalian brain
- MB-3 (drug) – Chemical compound

