<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(46)</volume><submitter>Yıldırım H</submitter><pubmed_abstract>Our previous studies have revealed that the aminated 1,4-quinone scaffold can be used for the development of novel antibacterial and/or antifungal agents. In this study, the aminated quinolinequinones (&lt;b>AQQ1-9&lt;/b>) were designed, synthesized, and evaluated for their antimicrobial activity against a panel of seven bacterial strains (three Gram-positive and four Gram-negative bacteria) and three fungal strains. The structure-activity relationship (SAR) for the QQs was also summarized. The antibacterial activity results indicated that the two aminated QQs (&lt;b>AQQ6&lt;/b> and &lt;b>AQQ9&lt;/b>) were active against &lt;i>Enterococcus faecalis&lt;/i> (ATCC 29212) with a MIC value of 78.12 μg/mL. Besides, the two aminated QQs (&lt;b>AQQ8&lt;/b> and &lt;b>AQQ9&lt;/b>) were active against &lt;i>Staphylococcus aureus&lt;/i> (ATCC</pubmed_abstract><journal>ACS omega</journal><pagination>41915-41928</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9685608</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aminated Quinolinequinones as Privileged Scaffolds for Antibacterial Agents: Synthesis, &lt;i>In Vitro&lt;/i> Evaluation, and Putative Mode of Action.</pubmed_title><pmcid>PMC9685608</pmcid><pubmed_authors>Yıldırım H</pubmed_authors><pubmed_authors>Jayaprakash V</pubmed_authors><pubmed_authors>Korkmaz S</pubmed_authors><pubmed_authors>Mataracı-Kara E</pubmed_authors><pubmed_authors>Bayrak N</pubmed_authors><pubmed_authors>Yıldız M</pubmed_authors><pubmed_authors>TuYuN AF</pubmed_authors><pubmed_authors>Shilkar D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aminated Quinolinequinones as Privileged Scaffolds for Antibacterial Agents: Synthesis, &lt;i>In Vitro&lt;/i> Evaluation, and Putative Mode of Action.</name><description>Our previous studies have revealed that the aminated 1,4-quinone scaffold can be used for the development of novel antibacterial and/or antifungal agents. In this study, the aminated quinolinequinones (&lt;b>AQQ1-9&lt;/b>) were designed, synthesized, and evaluated for their antimicrobial activity against a panel of seven bacterial strains (three Gram-positive and four Gram-negative bacteria) and three fungal strains. The structure-activity relationship (SAR) for the QQs was also summarized. The antibacterial activity results indicated that the two aminated QQs (&lt;b>AQQ6&lt;/b> and &lt;b>AQQ9&lt;/b>) were active against &lt;i>Enterococcus faecalis&lt;/i> (ATCC 29212) with a MIC value of 78.12 μg/mL. Besides, the two aminated QQs (&lt;b>AQQ8&lt;/b> and &lt;b>AQQ9&lt;/b>) were active against &lt;i>Staphylococcus aureus&lt;/i> (ATCC</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-04T19:51:38.495Z</modification><creation>2025-04-04T19:51:38.495Z</creation></dates><accession>S-EPMC9685608</accession><cross_references><pubmed>36440112</pubmed><doi>10.1021/acsomega.2c03193</doi></cross_references></HashMap>