N-9-fluorenylmethoxycarbonyl-Se-4-methoxybenzylselenocysteine

• CAT Number: M096630
• CAS Number: 150308-80-8
• Molecular Formula: C26H25NO5Se
• Molecular Weight: 510.46
• Purity: ≥95%
• Storage: -20°C
• IUPAC Name: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(4-methoxyphenyl)methylselanyl]propanoic acid
• InChI: InChI=1S/C26H25NO5Se/c1-31-18-12-10-17(11-13-18)15-33-16-24(25(28)29)27-26(30)32-14-23-21-8-4-2-6-19(21)20-7-3-5-9-22(20)23/h2-13,23-24H,14-16H2,1H3,(H,27,30)(H,28,29)/t24-/m0/s1
• InChIKey: XCPAYIZRJRMXBI-DEOSSOPVSA-N
• SMILES: COC1=CC=C(C=C1)C[Se]CC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

N-9-Fluorenylmethoxycarbonyl-Se-4-methoxybenzylselenocysteine（Cat No.:M096630） is a complex amino acid derivative incorporating selenium, designed for specialized biochemical and medicinal applications. The molecule features an N-9-fluorenyl methoxycarbonyl (Fmoc) protective group, commonly used in peptide synthesis to protect the amino group during chain assembly. The Se-4-methoxybenzyl group protects the selenium-containing side chain, enhancing the compound’s stability and reactivity. This selenocysteine derivative is particularly interesting in the study of proteins that naturally contain selenium, as it allows for the exploration of the role of selenium in biological systems and the design of novel antioxidants or therapeutic agents.