| Weight | 89.094 g/mol |
|---|---|
| Formula | C3H7NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
beta-alanine (107-95-9)
beta Alanine · 3-Aminopropionic Acid · beta Alanine, Monopotassium Salt
Score:
#1134 in Biochemistry
,
#2885 in Biology
,
#3611 in Chemistry
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- Cloning and expression of a cDNA encoding the transporter of taurine and beta-alanine in mouse brain (Proceedings of the National Academy of Sciences of the United States of America, 1992)
- A Staphylococcus aureus autolysin that has an N-acetylmuramoyl-L-alanine amidase domain and an endo-beta-N-acetylglucosaminidase domain: cloning, sequence analysis, and characterization (Proceedings of the National Academy of Sciences of the United States of America, 1995)
- Occurrence of beta-methylamino-l-alanine (BMAA) in ALS/PDC patients from Guam. (Acta Neurologica Scandinavica, 2004)
- Structure of -poly-l-alanine: Refined atomic co-ordinates for an anti-parallel beta-pleated sheet (Journal of Molecular Biology, 1967)
- Intramolecular Hydrogen Bonding in Derivatives of .beta.-Alanine and .gamma.-Amino Butyric Acid; Model Studies for the Folding of Unnatural Polypeptide Backbones (Journal of the American Chemical Society, 1994)
- Ampd, Essential for Both Beta-Lactamase Regulation and Cell Wall Recycling, Is a Novel Cytosolic N-Acetylmuramyl-L-Alanine Amidase (Molecular Microbiology, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - beta Alanine
- 3-Aminopropionic Acid
- beta Alanine, Monopotassium Salt
- beta Alanine, Monosodium Salt
- beta-Alanine, Monopotassium Salt
- beta-Alanine Hydrochloride
- 3 Aminopropionic Acid
- beta Alanine Hydrochloride
- beta-Alanine, Monosodium Salt
- beta-Alanine, Calcium Salt (2:1)
-
SMILESC(CN)C(=O)O
-
InChIKeyUCMIRNVEIXFBKS-UHFFFAOYSA-N
- Pubchem - beta-alanine
- Wikipedia - -alanine
-Alanine (or beta-alanine) is a naturally occurring beta amino acid, which is an amino acid in which the amino group is at the -position from the carboxylate group (i.e., two atoms away, see Figure 1). The IUPAC name for -alanine is 3-aminopropanoic acid. Unlike its counterpart -alanine, -alanine has no stereocenter.
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beta-alanine
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