Ac-Lys(Ac)-D-Ala-D-Ala-OH includes D-residues and an acetylated lysine, altering stereochemistry and charge characteristics. The peptide provides a model for studying recognition of modified motifs. Its structure supports folding and interaction analyses. Applications include peptide engineering and structure-activity exploration.
CAT No: D1204
CAS No:24570-39-6
Synonyms/Alias:(Ac)2-L-Lys-D-Ala-D-Ala;24570-39-6;Ac-Lys(Ac)-D-Ala-D-Ala-OH;CHEBI:270;CHEMBL353896;(Ac)2-L-lysyl-D-alanyl-D-alanine;(2R)-2-[[(2R)-2-[[(2S)-2,6-diacetamidohexanoyl]amino]propanoyl]amino]propanoic acid;AC1L48UX;Nalpha,Nepsilon-Diacetyl-Lys-D-Ala-D-Ala;C03326;SCHEMBL838549;FA110847;Q27105287;Nalpha,Nepsilon-Diacetyl-Lys-D-Ala-D-Ala, carboxypeptidase substrate;(R)-2-((R)-2-((S)-2,6-Diacetamidohexanamido)propanamido)propanoicacid;
1. Cationic cell-penetrating peptides are potent furin inhibitors
5. TMEM16F and dynamins control expansive plasma membrane reservoirs
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