Fmoc-O-(benzylphospho)-L-serine

• CAT Number: M095289
• CAS Number: 158171-14-3
• Molecular Formula: C25H24NO8P
• Molecular Weight: 497.44
• Purity: ≥95%
• Storage: -20°C
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[hydroxy(phenylmethoxy)phosphoryl]oxypropanoic acid
• InChI: InChI=1S/C25H24NO8P/c27-24(28)23(16-34-35(30,31)33-14-17-8-2-1-3-9-17)26-25(29)32-15-22-20-12-6-4-10-18(20)19-11-5-7-13-21(19)22/h1-13,22-23H,14-16H2,(H,26,29)(H,27,28)(H,30,31)/t23-/m0/s1
• InChIKey: ZBPUWGDUVAAWJY-QHCPKHFHSA-N
• SMILES: C1=CC=C(C=C1)COP(=O)(O)OCC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

Fmoc-O-(benzylphospho)-L-serine（Cat No.:M095289）, is a specialized compound used in peptide synthesis and biochemistry research. It belongs to the family of Fmoc (Fluorenylmethyloxycarbonyl) amino acids, which are crucial building blocks for creating peptides and proteins. This particular compound features a phosphodiester modification with a benzyl-protecting group, allowing for precise and controlled incorporation of phosphoserine into peptide sequences. Phosphorylated amino acids like this play essential roles in signal transduction and protein function. Researchers use Fmoc-O-(benzylphospho)-L-serine to study the effects of phosphorylation on protein structure and function and to develop novel peptides and biomolecules for various applications in biology and medicine.