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@ARTICLE{Klika:167329,
author = {K. Klika$^*$ and C. Da Pieve and K. Kopka and G. Smith and
A. Makarem$^*$},
title = {{S}ynthesis and application of a thiol-reactive {HBED}-type
chelator for development of easy-to-produce
{G}a-radiopharmaceutical kits and imaging probes.},
journal = {Organic $\&$ biomolecular chemistry},
volume = {19},
number = {8},
issn = {1477-0539},
address = {Cambridge},
publisher = {Royal Society of Chemistry},
reportid = {DKFZ-2021-00277},
pages = {1722-1726},
year = {2021},
note = {#EA:A390#LA:E030# /Division of Radiopharmaceutical
Chemistry,2021 Mar 4;19(8):1722-1726},
abstract = {In radiopharmaceutical syntheses, maleimide is commonly
used for linking thiol-bearing bioactive molecules to
metal-complexing ligands (chelators). However, due to
instability of the resulting linkage, phenyloxadiazolyl
methylsulfone (PODS) was developed as an alternative to
maleimide. This coupling strategy has never been attempted
with HBED which is a powerful chelator for
gallium-radiolabeling especially at ambient temperature.
Here we present HBED-CC-PODS as a bifunctional chelator
scaffold for the site-selective conjugation of thiol-bearing
vectors and [68Ga]Ga-radiolabeling.},
cin = {A390 / E030},
ddc = {540},
cid = {I:(DE-He78)A390-20160331 / I:(DE-He78)E030-20160331},
pnm = {315 - Bildgebung und Radioonkologie (POF4-315)},
pid = {G:(DE-HGF)POF4-315},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:33527964},
doi = {10.1039/D0OB02513E},
url = {https://inrepo02.dkfz.de/record/167329},
}