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Supplier: Thermo Scientific Chemicals
Description: 99%
Catalog Number: (TCA0323-100G)
Supplier: TCI America
Description: CAS Number: 62-57-7
MDL Number: MFCD00008049
Molecular Formula: C4H9NO2
Molecular Weight: 103.12
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 335

Supplier: Ambeed
Description: DL-3-Aminoisobutyric acid hydrate 95%

Supplier: Adipogen
Description: Catabolite of thymine. Precursor for 3-Hydroxyisobutyric acid synthesis. Small molecule myokine. Browning inducer of white adipose tissue (WAT) into brown adipose tissue (BAT). PGC-1alpha-mediated and exercise-triggered nonadrenergic activator of the thermogenic program in WAT. Increases the expression of brown adipocyte-specific genes (browning) in white adipocytes and beta-oxidation in hepatocytes through a PPARalpha-mediated mechanism. Induces a brown adipose-like phenotype in human pluripotent stem cells and improves glucose homeostasis. Enhances fatty acid oxidation and reduces body weight in mice through an increased production of leptin by the white adipose tissue (WAT). Inhibits Agxt2-mediated metabolism of dimethylarginines. Partial agonist of the glycine receptor (GlyR).

Supplier: Sigma Aldrich
Description: 25G CAS 62-57-7

Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 037475-100G , MDL Number: MFCD00008049

Supplier: Bachem Americas
Description: Sequence: H-Aib-OtBu · HCl
Synonym(s): H-α-Me-Ala-OtBu · HCl

Supplier: Ambeed
Description: 2-Amino-2-methylpropanoic acid, Purity: 98%, CAS Number: 62-57-7, Appearance: Form: Crystal - Powder / Colour: White to Off white, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 25G
Supplier: Matrix Scientific
Description: Matrix Scientific Part Number: 041576-1G , MDL Number: MFCD01863213

Supplier: TLC Standards
Description: Pharmaceutical Standards, 2-Methylalanine (2-Aminoisobutyric Acid)

New Product

Supplier: TCI America
Description: CAS Number: 144-90-1 MDL Number: MFCD00008145 Molecular Formula: C4H9NO2 Molecular Weight: 103.12 Purity/Analysis Method: <gt/>98.0% (T) Form: Crystal Melting point (°C): 174
Supplier: Adipogen
Description: Beta-Aminoisobutyric acid is a non-protein amino acid originating from the catabolism of thymine and valine. beta-Aminoisobutyric acid occurs in two isomeric forms and both enantiomers of beta-Aminoisobutyric acid can be detected in human urine and plasma. In plasma, the S-enantiomer is the predominant type due to active renal reabsorption. In contrast, urine almost exclusively contains the R-enantiomer of beta-Aminoisobutyric acid, which is eliminated both by filtration and tubular secretion. The S-enantiomer of beta-Aminoisobutyric acid is predominantly derived from the catabolism of valine, the R-enantiomer is the product of the catabolism of the pyrimidine bases uracil and thymine by the enzyme dihydropyrimidine dehydrogenase (DPD), in what constitutes the first step of the pyrimidine degradation pathway. Transient high levels of beta-Aminoisobutyric acid have been observed under a variety of pathological conditions such as lead poisoning, starvation, in total body irradiation and in a number of malignancies. Recently R-/S-enantiomer mixtures have been shown to be browning inducer of white adipose tissue.

Supplier: Ambeed
Description: S-BAIBA 95%

New Product

Supplier: Thermo Scientific Chemicals
Description: tert-Butyl 2-aminoisobutyrate hydrochloride, 98%
Supplier: Adipogen
Description: Beta-Aminoisobutyric acid is a non-protein amino acid originating from the catabolism of thymine and valine. beta-Aminoisobutyric acid occurs in two isomeric forms and both enantiomers of beta-Aminoisobutyric acid can be detected in human urine and plasma. In plasma, the S-enantiomer is the predominant type due to active renal reabsorption. In contrast, urine almost exclusively contains the R-enantiomer of beta-Aminoisobutyric acid, which is eliminated both by filtration and tubular secretion. The S-enantiomer of beta-Aminoisobutyric acid is predominantly derived from the catabolism of valine, the R-enantiomer is the product of the catabolism of the pyrimidine bases uracil and thymine by the enzyme dihydropyrimidine dehydrogenase (DPD), in what constitutes the first step of the pyrimidine degradation pathway. Transient high levels of beta-Aminoisobutyric acid have been observed under a variety of pathological conditions such as lead poisoning, starvation, in total body irradiation and in a number of malignancies. Recently R-/S-enantiomer mixtures have been shown to be browning inducer of white adipose tissue.

Catalog Number: (75789-096)
Supplier: Prosci
Description: beta -Ureidopropionase is a cytoplasmic protein which belongs to the CN hydrolase family of BUP subfamily. beta -Ureidopropionase binds one zinc ion per subunit, catalyzes the last step in the pyrimidine degradation pathway. beta -Ureidopropionase can convert N-carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta-alanine to beta-aminoisobutyric acid and beta-alanine, ammonia and carbon dioxide, respectively. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta aminoisobutyric acid, respectively. Defects in beta -Ureidopropionase are the cause of beta -Ureidopropionase deficiency that is characterized by muscular hypotonia, dystonic movements, scoliosis, microcephaly and severe developmental delay.


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