<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(23)</volume><submitter>Doloczki S</submitter><pubmed_abstract>In this work, a series of fluorescent 2,1,3-benzothiadiazole derivatives with various &lt;i>N&lt;/i>-substituents in the 4-position was synthesized and photophysically characterized in various solvents. Three compounds emerged as excellent fluorescent probes for imaging lipid droplets in cancer cells. A correlation between their high lipophilicity and lipid droplet specificity could be found, with log &lt;i>P&lt;/i> ≥ 4 being characteristic for lipid droplet accumulation.</pubmed_abstract><journal>RSC advances</journal><pagination>14544-14550</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9101220</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Photophysical characterization and fluorescence cell imaging applications of 4-&lt;i>N&lt;/i>-substituted benzothiadiazoles.</pubmed_title><pmcid>PMC9101220</pmcid><pubmed_authors>Dyrager C</pubmed_authors><pubmed_authors>Swartling FJ</pubmed_authors><pubmed_authors>Doloczki S</pubmed_authors><pubmed_authors>Holmberg KO</pubmed_authors><pubmed_authors>Fdez Galvan I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Photophysical characterization and fluorescence cell imaging applications of 4-&lt;i>N&lt;/i>-substituted benzothiadiazoles.</name><description>In this work, a series of fluorescent 2,1,3-benzothiadiazole derivatives with various &lt;i>N&lt;/i>-substituents in the 4-position was synthesized and photophysically characterized in various solvents. Three compounds emerged as excellent fluorescent probes for imaging lipid droplets in cancer cells. A correlation between their high lipophilicity and lipid droplet specificity could be found, with log &lt;i>P&lt;/i> ≥ 4 being characteristic for lipid droplet accumulation.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-18T16:45:19.579Z</modification><creation>2024-11-12T01:37:39.61Z</creation></dates><accession>S-EPMC9101220</accession><cross_references><pubmed>35702197</pubmed><doi>10.1039/d2ra01404a</doi></cross_references></HashMap>