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Syntheses of bifunctional 2,3-diamino propionic acid-based chelators as small and strong tripod ligands for the labelling of biomolecules with (99m)Tc.

Authors :
Liu Y
Oliveira BL
Correia JD
Santos IC
Santos I
Spingler B
Alberto R
Source :
Organic & biomolecular chemistry [Org Biomol Chem] 2010 Jun 21; Vol. 8 (12), pp. 2829-39. Date of Electronic Publication: 2010 May 06.
Publication Year :
2010

Abstract

The labelling of targeting biomolecules requires small and hydrophilic complexes in order to not affect the binding properties of the vectors. 2,3-Diamino propionic acid (dap) is a small and strong, albeit scarcely used, tripod ligand for the fac-[(99m)Tc(CO)(3)](+) moiety. We have introduced at the alpha-carbon atom in the basic dap structure various second functionalities such as carboxylato, amino and alpha-amino acid groups via various spacers in order to yield bifunctional chelators. These dap derivatives can be coupled to targeting molecules for application in molecular imaging. Full characterizations of the bifunctional chelators, X-ray structures of intermediates and of one rhenium complex, as well as labelling studies with (99m)Tc, are presented.

Details

Language :
English
ISSN :
1477-0539
Volume :
8
Issue :
12
Database :
MEDLINE
Journal :
Organic & biomolecular chemistry
Publication Type :
Academic Journal
Accession number :
20445942
Full Text :
https://doi.org/10.1039/c002796k