Publication:

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

Date

Date

Date
2010
Journal Article
Published version
cris.lastimport.scopus2025-07-14T03:41:41Z
cris.lastimport.wos2025-08-05T01:38:28Z
cris.virtual.orcidhttps://orcid.org/0000-0003-3402-2016
cris.virtual.orcidhttps://orcid.org/0000-0001-5978-3394
cris.virtualsource.orcid0aba17af-b4fc-4715-a5a7-6236ee495ce1
cris.virtualsource.orcidb2df8e24-7f16-4248-a74b-93c141285dab
dc.contributor.institutionUniversity of Zurich
dc.date.accessioned2011-02-23T17:24:44Z
dc.date.available2011-02-23T17:24:44Z
dc.date.issued2010
dc.description.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-Tc-99m(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 Tc-99m, are presented.

dc.identifier.doi10.1039/c002796k
dc.identifier.issn1477-0520
dc.identifier.otherISI:000278964600020
dc.identifier.scopus2-s2.0-77953176831
dc.identifier.urihttps://www.zora.uzh.ch/handle/20.500.14742/59830
dc.identifier.wos000278964600020
dc.language.isoeng
dc.subject.ddc540 Chemistry
dc.title

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

dc.typearticle
dcterms.accessRightsinfo:eu-repo/semantics/closedAccess
dcterms.bibliographicCitation.journaltitleOrganic & Biomolecular Chemistry
dcterms.bibliographicCitation.number12
dcterms.bibliographicCitation.originalpublishernameRoyal Society of Chemistry
dcterms.bibliographicCitation.originalpublisherplaceTHOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND
dcterms.bibliographicCitation.pageend2839
dcterms.bibliographicCitation.pagestart2829
dcterms.bibliographicCitation.pmid20445942
dcterms.bibliographicCitation.volume8
dspace.entity.typePublicationen
uzh.contributor.affiliationUniversity of Zurich
uzh.contributor.affiliationInstituto Tecnológico E Nuclear
uzh.contributor.affiliationInstituto Tecnológico E Nuclear
uzh.contributor.affiliationInstituto Tecnológico E Nuclear
uzh.contributor.affiliation#PLACEHOLDER_PARENT_METADATA_VALUE#
uzh.contributor.affiliationUniversity of Zurich
uzh.contributor.affiliationUniversity of Zurich
uzh.contributor.authorLiu, Y
uzh.contributor.authorOliveira, B L
uzh.contributor.authorCorreia, J D G
uzh.contributor.authorSantos, I C
uzh.contributor.authorSantos, I
uzh.contributor.authorSpingler, B
uzh.contributor.authorAlberto, R
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceNo
uzh.contributor.correspondenceYes
uzh.document.availabilityno_document
uzh.eprint.datestamp2011-02-23 17:24:44
uzh.eprint.lastmod2025-08-05 01:52:52
uzh.eprint.statusChange2011-02-23 17:24:44
uzh.harvester.ethNo
uzh.harvester.nbNo
uzh.jdb.eprintsId17017
uzh.oastatus.unpaywallclosed
uzh.oastatus.zoraClosed
uzh.publication.citationLiu, Y; Oliveira, B L; Correia, J D G; Santos, I C; Santos, I; Spingler, B; Alberto, R (2010). Syntheses of bifunctional 2,3-diamino propionic acid-based chelators as small and strong tripod ligands for the labelling of biomolecules with (99m)Tc. Organic & Biomolecular Chemistry, 8(12):2829-2839.
uzh.publication.originalworkoriginal
uzh.publication.publishedStatusfinal
uzh.scopus.impact13
uzh.scopus.subjectsBiochemistry
uzh.scopus.subjectsPhysical and Theoretical Chemistry
uzh.scopus.subjectsOrganic Chemistry
uzh.workflow.eprintid46264
uzh.workflow.fulltextStatusnone
uzh.workflow.revisions54
uzh.workflow.rightsCheckkeininfo
uzh.workflow.statusarchive
uzh.wos.impact13
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