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CAS 3227-17-6

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(2S)-2-ammonio-2-methylbutanedioate

Description:
(2S)-2-ammonio-2-methylbutanedioate, also known as L-2-amino-4-methylpentanedioate, is an amino acid derivative characterized by its chiral center, which contributes to its specific stereochemistry. This compound features a carboxylate group, making it an acidic substance, and an ammonium group, which imparts basic properties. It is typically found in a zwitterionic form at physiological pH, where it carries both a positive and a negative charge. This dual charge enhances its solubility in water and its ability to participate in various biochemical reactions. The presence of the methyl group contributes to its hydrophobic characteristics, influencing its interactions in biological systems. As a derivative of aspartic acid, it plays a role in metabolic pathways and can be involved in the synthesis of other biomolecules. Its unique structure allows it to participate in enzyme-catalyzed reactions and serve as a building block in protein synthesis. Overall, (2S)-2-ammonio-2-methylbutanedioate is significant in biochemistry and molecular biology due to its functional properties and roles in metabolic processes.
Formula:C5H8NO4
InChI:InChI=1/C5H9NO4/c1-5(6,4(9)10)2-3(7)8/h2,6H2,1H3,(H,7,8)(H,9,10)/p-1/t5-/m0/s1
SMILES:C[C@](CC(=O)[O-])(C(=O)O)N
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