902314

[CpRu(Fmoc-tyrosin)]CF₃CO₂

• Synonyme(s) : Fmoc-protected ruthenium tyrosine amino acid derivative, Peptide radiolabel precursor, [18F]Fluorophenylalanine peptide residue precursor
• Formule empirique (notation de Hill): C₃₁H₂₆F₃NO₇Ru
• Poids moléculaire : 682.61
• Code UNSPSC : 12352209
• Nomenclature NACRES : NA.26

Propriétés

• Forme: powder
• Capacité de réaction: reaction type: Fmoc solid-phase peptide synthesis
• Pf: >300 °C
• Application(s): peptide synthesis
• Groupe fonctionnel: Fmoc
• Température de stockage: 2-8°C
• Chaîne SMILES: O[C]1[CH][CH][C](CC(NC(OCC2C(C=CC=C3)=C3C4=C2C=CC=C4)=O)C(O)=O)[CH][CH]1.F[C-](F)F.O=C=O.[Ru+].c5cccc5

Description

Application

The Ritter lab has developed a new method for direct labeling of polypeptides with the [18F]fluoride radiolabel. This Fmoc-protected ruthenium tyrosine is first incorporated into peptides, which is amenable to standard solid-phase peptide synthesis (SPPS) and is tolerant of all 20 canonical amino acids. Subsequent replacement of a single hydrogen with fluorine-18, with only minimal perturbation of the peptide structure, results in a site-specific, radiolabeled peptide tracer for use with positron emission tomography (PET) imaging in the study of various biological applications.

Attention

Research quantities limited to 10 g.

Autres remarques

Site-SpecificDeoxyfluorination of Small Peptides with [18F]Fluoride

Informations légales

Patent Application EP18204755.5
This product is manufactured pursuant to a license with Studiengesellschaft Kohle mbH

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable