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CAS 61548-53-6

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6-Amino-5-hydroxy-2-pyridinecarboxylic acid

Description:
6-Amino-5-hydroxy-2-pyridinecarboxylic acid, commonly known as L-5-hydroxylysine, is an organic compound characterized by its pyridine ring structure, which contains both amino and hydroxyl functional groups. This compound is a derivative of pyridinecarboxylic acid and is notable for its role in biochemical processes, particularly in the synthesis of certain amino acids and proteins. It exhibits properties typical of amino acids, such as the ability to form zwitterions, which can influence its solubility and reactivity in various environments. The presence of the hydroxyl group contributes to its potential as a chelating agent, allowing it to interact with metal ions. Additionally, its amino group can participate in hydrogen bonding, enhancing its interactions in biological systems. This compound is of interest in pharmaceutical and biochemical research due to its potential applications in drug development and as a biochemical marker. Overall, 6-Amino-5-hydroxy-2-pyridinecarboxylic acid is a versatile compound with significant implications in both chemistry and biology.
Formula:C6H6N2O3
InChI:InChI=1/C6H6N2O3/c7-5-4(9)2-1-3(8-5)6(10)11/h1-2,9H,(H2,7,8)(H,10,11)
InChI key:InChIKey=RQGZPPDRBLARLZ-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1N=C(N)C(O)=CC1
Synonyms:
  • 2-Pyridinecarboxylic Acid, 6-Amino-5-Hydroxy-
  • 6-Amino-5-hydroxy-2-pyridinecarboxylic acid
  • 6-Amino-5-hydroxypyridine-2-carboxylic acid
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