Fmoc-N'-Acetyl-L-lysine

• CAT Number: M035533
• CAS Number: 159766-56-0
• Molecular Formula: C23H26N2O5
• Molecular Weight: 410.47
• Purity: ≥95%
• Storage: Desiccate at -20℃
• IUPAC Name: (2S)-6-acetamido-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
• InChI: InChI=1S/C23H26N2O5/c1-15(26)24-13-7-6-12-21(22(27)28)25-23(29)30-14-20-18-10-4-2-8-16(18)17-9-3-5-11-19(17)20/h2-5,8-11,20-21H,6-7,12-14H2,1H3,(H,24,26)(H,25,29)(H,27,28)/t21-/m0/s1
• InChIKey: HQLBYVWJOXITAM-NRFANRHFSA-N
• SMILES: CC(=O)NCCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Fmoc-N’-Acetyl-L-lysine (Cat No.: M035533) is a protected derivative of the amino acid L-lysine, where the α-amino group is blocked with a 9-fluorenylmethyloxycarbonyl (Fmoc) group and the ε-amino side chain is acetylated. This structure is widely used in solid-phase peptide synthesis (SPPS) to incorporate post-translational modifications such as lysine acetylation, which is important in epigenetics and protein regulation. It enables the study of histone modifications, protein–protein interactions, and biological pathways involving acetylated lysine residues in biochemical and pharmaceutical research.