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Alanine (symbol Ala or A), [4] or α-alanine, is an α-amino acid that is used in the biosynthesis of proteins. It contains an amine group and a carboxylic acid group, both attached to the central carbon atom which also carries a methyl group side chain. Consequently it is classified as a nonpolar, aliphatic α-amino acid.
β-Alanine (beta-alanine) is a naturally occurring beta amino acid, which is an amino acid in which the amino group is attached to the β-carbon (i.e. the carbon two carbon atoms away from the carboxylate group) instead of the more usual α-carbon for alanine (α-alanine). The IUPAC name for β-alanine is 3-aminopropanoic acid.
3-Aminopropionic acid, or β-alanine This page was last edited on 8 October 2024, at 03:48 (UTC). Text is available under the Creative Commons Attribution-ShareAlike ...
{α/2}-aminopropionic acid AIDS{-}071780 HSDB 1801 ... ^a EINECS for L-alanine ^a CID 602 from PubChem ^a CID 5950 from PubChem This page was last edited on 12 ...
In addition to the common amino acid L-tyrosine, which is the para isomer (para-tyr, p-tyr or 4-hydroxyphenylalanine), there are two additional regioisomers, namely meta-tyrosine (also known as 3-hydroxyphenylalanine, L-m-tyrosine, and m-tyr) and ortho-tyrosine (o-tyr or 2-hydroxyphenylalanine), that occur in nature.
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Still, Holbrook was initially apprehensive about playing such an iconic musician. "I was shocked and a little daunted," he recalls of his response to Mangold's offer for the role.