<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hoerres R</submitter><funding>U.S. Nuclear Regulatory Commission</funding><pagination>20688-20698</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10732151</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(50)</volume><pubmed_abstract>Metal complexes with the general formula [M&lt;sup>I&lt;/sup>(CO)&lt;sub>3&lt;/sub>(k&lt;sup>3&lt;/sup>-L)]&lt;sup>+&lt;/sup>, where M = Re, &lt;sup>186&lt;/sup>Re, or &lt;sup>99m&lt;/sup>Tc and L = 1,4,7-triazacyclononane (TACN), NOTA, or NODAGA chelators, have previously been conjugated to peptide-based biological targeting vectors and investigated as potential theranostic radiopharmaceuticals. The promising results demonstrated by these bioconjugate complexes prompted our exploration of other TACN-based chelators for suitability for (radio)labeling with the [M(CO)&lt;sub>3&lt;/sub>]&lt;sup>+&lt;/sup> core. In this work, we investigated the role of the TACN pendant arms in complexation of the [M(CO)&lt;sub>3&lt;/sub>]&lt;sup>+&lt;/sup> core through (radio)labeling of TACN chelators bearing acid, ester, mixed acid-ester, or no pendant functional g</pubmed_abstract><journal>Inorganic chemistry</journal><pubmed_title>1,4,7-Triazacyclononane-Based Chelators for the Complexation of [&lt;sup>186&lt;/sup>Re]Re- and [&lt;sup>99m&lt;/sup>Tc]Tc-Tricarbonyl Cores.</pubmed_title><pmcid>PMC10732151</pmcid><funding_grant_id>31310021M0040</funding_grant_id><pubmed_authors>Hennkens HM</pubmed_authors><pubmed_authors>Hoerres R</pubmed_authors></additional><is_claimable>false</is_claimable><name>1,4,7-Triazacyclononane-Based Chelators for the Complexation of [&lt;sup>186&lt;/sup>Re]Re- and [&lt;sup>99m&lt;/sup>Tc]Tc-Tricarbonyl Cores.</name><description>Metal complexes with the general formula [M&lt;sup>I&lt;/sup>(CO)&lt;sub>3&lt;/sub>(k&lt;sup>3&lt;/sup>-L)]&lt;sup>+&lt;/sup>, where M = Re, &lt;sup>186&lt;/sup>Re, or &lt;sup>99m&lt;/sup>Tc and L = 1,4,7-triazacyclononane (TACN), NOTA, or NODAGA chelators, have previously been conjugated to peptide-based biological targeting vectors and investigated as potential theranostic radiopharmaceuticals. The promising results demonstrated by these bioconjugate complexes prompted our exploration of other TACN-based chelators for suitability for (radio)labeling with the [M(CO)&lt;sub>3&lt;/sub>]&lt;sup>+&lt;/sup> core. In this work, we investigated the role of the TACN pendant arms in complexation of the [M(CO)&lt;sub>3&lt;/sub>]&lt;sup>+&lt;/sup> core through (radio)labeling of TACN chelators bearing acid, ester, mixed acid-ester, or no pendant functional g</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-18T21:41:58.397Z</modification><creation>2025-02-19T02:33:51.172Z</creation></dates><accession>S-EPMC10732151</accession><cross_references><pubmed>37683190</pubmed><doi>10.1021/acs.inorgchem.3c01934</doi></cross_references></HashMap>