Reagents for Peptide Synthesis

Fmoc protected N-trimethyl lysineApplicationFmoc-Lys(Me)3-OH chloride is one of the common N-terminal protected reagents used in the peptide synthesis. Some of the reported examples are:Synthesis of peptide linkers for monoclonal antibody-auristatin

Fmoc protected N-trimethyl lysineApplicationFmoc-Lys(Me)3-OH chloride is one of the common N-terminal protected reagents used in the peptide synthesis. Some of the reported examples are:Synthesis of peptide linkers for monoclonal antibody-auristatin

Fmoc protected N-trimethyl lysineApplicationFmoc-Lys(Me)3-OH chloride is one of the common N-terminal protected reagents used in the peptide synthesis. Some of the reported examples are:Synthesis of peptide linkers for monoclonal antibody-auristatin

Fmoc protected N-trimethyl lysineApplicationFmoc-Lys(Me)3-OH chloride is one of the common N-terminal protected reagents used in the peptide synthesis. Some of the reported examples are:Synthesis of peptide linkers for monoclonal antibody-auristatin

Fmoc protected N-trimethyl lysineApplicationFmoc-Lys(Me)3-OH chloride is one of the common N-terminal protected reagents used in the peptide synthesis. Some of the reported examples are:Synthesis of peptide linkers for monoclonal antibody-auristatin

DescriptionA novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS [1, 2]. Coupling can be carried out using any standard activation method. Removal of the Boc protecting group occurs during the course of the TFA-mediated

DescriptionA novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS [1, 2]. Coupling can be carried out using any standard activation method. Removal of the Boc protecting group occurs during the course of the TFA-mediated

DescriptionA novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS [1, 2]. Coupling can be carried out using any standard activation method. Removal of the Boc protecting group occurs during the course of the TFA-mediated

DescriptionA novel derivative for the introduction of monomethyl-lysine during Fmoc SPPS [1, 2]. Coupling can be carried out using any standard activation method. Removal of the Boc protecting group occurs during the course of the TFA-mediated

Fmoc-Lys-OH

Fmoc-Lys-OH

Fmoc-Lys-OH