FMOC-D-TYR(PO3H2)-OH, also known as FMOC-D-Tyrosine phosphate, is a derivative of the amino acid tyrosine that has been modified to include a phosphate group and a 9-fluorenylmethoxycarbonyl (FMOC) protecting group. This compound is characterized by its ability to participate in peptide synthesis, particularly in the formation of phosphopeptides, which are important in various biological processes. The FMOC group serves as a protective moiety that can be removed under mild basic conditions, allowing for selective deprotection during peptide synthesis. The phosphate group enhances the compound's solubility in polar solvents and contributes to its biological activity, as phosphorylation is a key post-translational modification in cellular signaling. FMOC-D-TYR(PO3H2)-OH is typically used in research and development within the fields of biochemistry and medicinal chemistry, particularly in studies involving protein interactions and signaling pathways. Its stability, reactivity, and ability to mimic natural phosphotyrosine residues make it a valuable tool in synthetic chemistry and bioconjugation applications.

FMOC-D-TYR(PO3H2)-OH

178432-30-9: FMOC-D-TYR(PO3H2)-OH, also known as FMOC-D-Tyrosine phosphate, is a derivative of the amino acid tyrosine that has been modified to include a phosphate group and a 9-fluorenylmethoxycarbonyl (FMOC) protecting group. This compound is characterized by its ability to participate in peptide synthesis, particularly in the formation of phosphopeptides, which are important in various biological processes. The FMOC group serves as a protective moiety that can be removed under mild basic conditions, allowing for selective deprotection during peptide synthesis. The phosphate group enhances the compound's solubility in polar solvents and contributes to its biological activity, as phosphorylation is a key post-translational modification in cellular signaling. FMOC-D-TYR(PO3H2)-OH is typically used in research and development within the fields of biochemistry and medicinal chemistry, particularly in studies involving protein interactions and signaling pathways. Its stability, reactivity, and ability to mimic natural phosphotyrosine residues make it a valuable tool in synthetic chemistry and bioconjugation applications.

CAS 178432-30-9

FMOC-D-TYR(PO3H2)-OH

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-O-phosphono-D-tyrosine

Ref: IN-DA00261J

Fmoc-D-Tyr(PO3H2)-OH

Ref: 7W-GM8258