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CAS 203854-56-2

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(2S)-2-(Aminomethyl)-4-methylpentanoic acid

Description:
(2S)-2-(Aminomethyl)-4-methylpentanoic acid, commonly known as a derivative of the amino acid leucine, is characterized by its chiral center, which contributes to its specific stereochemistry. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), making it an α-amino acid. The presence of the aminomethyl group enhances its potential for biological activity, particularly in protein synthesis and metabolic pathways. It is soluble in water due to the polar nature of its functional groups, which allows it to interact favorably with aqueous environments. The compound's structure includes a branched alkyl chain, which can influence its hydrophobic properties and interactions with other biomolecules. As a result, it may play a role in various biochemical processes, including enzyme activity and cellular signaling. Its specific stereochemistry and functional groups make it a subject of interest in pharmaceutical and biochemical research, particularly in the development of therapeutics and nutritional supplements.
Formula:C7H15NO2
InChI:InChI=1S/C7H15NO2/c1-5(2)3-6(4-8)7(9)10/h5-6H,3-4,8H2,1-2H3,(H,9,10)/t6-/m0/s1
InChI key:InChIKey=IAXQYBCPMFDMOJ-LURJTMIESA-N
SMILES:[C@@H](CC(C)C)(C(O)=O)CN
Synonyms:
  • Pentanoic acid, 2-(aminomethyl)-4-methyl-, (2S)-
  • (2S)-2-(Aminomethyl)-4-methylpentanoic acid
  • (-)-2-Aminomethyl-4-methylpentanoic acid
  • (S)-2-Aminomethyl-4-methylpentanoic acid
  • Pentanoic acid, 2-(aminomethyl)-4-methyl-, (S)-
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