Na,ne-diacetyl-lys-D-ala-D-lactic acid, identified by its CAS number 65882-12-4, is a synthetic compound that features a combination of amino acids and acetyl groups. This substance is characterized by its structural complexity, which includes a lysine residue, two acetyl groups, and a lactic acid moiety. The presence of these functional groups suggests that it may exhibit both hydrophilic and hydrophobic properties, influencing its solubility and reactivity in various environments. Typically, compounds like this are studied for their potential applications in biochemistry and pharmaceuticals, particularly in drug design or as intermediates in the synthesis of more complex molecules. The diacetyl modification may enhance the stability or bioavailability of the compound, while the amino acid components could contribute to its biological activity. Overall, Na,ne-diacetyl-lys-D-ala-D-lactic acid represents a unique intersection of amino acid chemistry and synthetic organic chemistry, making it a subject of interest in various scientific fields.

na,ne-diacetyl-lys-D-ala-D-lactic acid

65882-12-4: Na,ne-diacetyl-lys-D-ala-D-lactic acid, identified by its CAS number 65882-12-4, is a synthetic compound that features a combination of amino acids and acetyl groups. This substance is characterized by its structural complexity, which includes a lysine residue, two acetyl groups, and a lactic acid moiety. The presence of these functional groups suggests that it may exhibit both hydrophilic and hydrophobic properties, influencing its solubility and reactivity in various environments. Typically, compounds like this are studied for their potential applications in biochemistry and pharmaceuticals, particularly in drug design or as intermediates in the synthesis of more complex molecules. The diacetyl modification may enhance the stability or bioavailability of the compound, while the amino acid components could contribute to its biological activity. Overall, Na,ne-diacetyl-lys-D-ala-D-lactic acid represents a unique intersection of amino acid chemistry and synthetic organic chemistry, making it a subject of interest in various scientific fields.

Ac₂Lys-D-Ala-D-Lac-OH is a depsipeptide substrate for penicillin-sensitive D-alanine carboxypeptidases (DD-carboxypeptidases).

Ac-Lys(Ac)-D-Ala-D-lactic acid

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CAS 65882-12-4

na,ne-diacetyl-lys-D-ala-D-lactic acid

Ac-Lys(Ac)-D-Ala-D-lactic acid

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Ac-Lys(Ac)-D-Ala-D-lactic acid

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