<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Demoin DW</submitter><funding>NCI NIH HHS</funding><pagination>606-11</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5363724</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(10)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Chemokine receptor-4 (CXCR4, fusin, CD184) is expressed on several tissues involved in immune regulation and is upregulated in many diseases including malignant gliomas. A radiolabeled small molecule that readily crosses the blood-brain barrier can aid in identifying CXCR4-expressing gliomas and monitoring CXCR4-targeted therapy. In the current work, we have synthesized and evaluated an [(18)F]-labeled small molecule based on a pyrimidine-pyridine amine for its ability to target CXCR4.&lt;h4>Experimental&lt;/h4>The nonradioactive standards and the nitro precursor used in this study were prepared using established methods. An HPLC method was developed to separate the nitro-precursor from the nonradioactive standard and radioactive product. The nitro-precursor was radiolabeled</pubmed_abstract><journal>Nuclear medicine and biology</journal><pubmed_title>Synthesis and evaluation of an (18)F-labeled pyrimidine-pyridine amine for targeting CXCR4 receptors in gliomas.</pubmed_title><pmcid>PMC5363724</pmcid><funding_grant_id>R01 CA172546</funding_grant_id><funding_grant_id>P50 CA086438</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>R01 CA163980</funding_grant_id><pubmed_authors>Shindo M</pubmed_authors><pubmed_authors>Demoin DW</pubmed_authors><pubmed_authors>Pillarsetty NV</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Serganova I</pubmed_authors><pubmed_authors>Blasberg RG</pubmed_authors><pubmed_authors>Edwards KJ</pubmed_authors><pubmed_authors>Lewis JS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and evaluation of an (18)F-labeled pyrimidine-pyridine amine for targeting CXCR4 receptors in gliomas.</name><description>&lt;h4>Introduction&lt;/h4>Chemokine receptor-4 (CXCR4, fusin, CD184) is expressed on several tissues involved in immune regulation and is upregulated in many diseases including malignant gliomas. A radiolabeled small molecule that readily crosses the blood-brain barrier can aid in identifying CXCR4-expressing gliomas and monitoring CXCR4-targeted therapy. In the current work, we have synthesized and evaluated an [(18)F]-labeled small molecule based on a pyrimidine-pyridine amine for its ability to target CXCR4.&lt;h4>Experimental&lt;/h4>The nonradioactive standards and the nitro precursor used in this study were prepared using established methods. An HPLC method was developed to separate the nitro-precursor from the nonradioactive standard and radioactive product. The nitro-precursor was radiolabeled</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2025-04-04T09:00:49.75Z</modification><creation>2019-03-27T02:39:25Z</creation></dates><accession>S-EPMC5363724</accession><cross_references><pubmed>27485481</pubmed><doi>10.1016/j.nucmedbio.2016.05.005</doi></cross_references></HashMap>