Ac-Lys(Ac)-D-Ala-D-Ala-OH

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.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

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;

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cGMP Peptide
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  • CMC information required for an IND
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M.F/Formula
C16H28N4O6
M.W/Mr.
372.42
Sequence
One Letter Code:XAA
Three Letter Code:Ac-Lys(Ac)-D-Ala-D-Ala-OH
InChI
InChI=1S/C16H28N4O6/c1-9(14(23)19-10(2)16(25)26)18-15(24)13(20-12(4)22)7-5-6-8-17-11(3)21/h9-10,13H,5-8H2,1-4H3,(H,17,21)(H,18,24)(H,19,23)(H,20,22)(H,25,26)/t9-,10-,13+/m1/s1
InChI Key
VIHGYLJIMMKSBR-BREBYQMCSA-N

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