<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(1)</volume><submitter>Khan BA</submitter><pubmed_abstract>New &lt;i>S&lt;/i>-alkyl phthalimide &lt;b>5a&lt;/b>-&lt;b>f&lt;/b> and &lt;i>S&lt;/i>-benzyl &lt;b>6a&lt;/b>-&lt;b>d&lt;/b> analogs of 5-(2-phenylquinolin-4-yl)-1,3,4-oxadiazole-2-thiol (&lt;b>4&lt;/b>) were prepared by reacting &lt;b>4&lt;/b> with &lt;i>N&lt;/i>-bromoalkylphthalimide and CF&lt;sub>3&lt;/sub>-substituted benzyl bromides in excellent yields. Spectroscopic techniques were employed to elucidate the structures of the synthesized molecules. The inhibition activity of newly synthesized molecules toward MAO-A, MAO-B, and AChE enzymes, was also assessed. All these compounds showed activity in the submicromolar range against all enzymes. Compounds &lt;b>5a&lt;/b> and &lt;b>5f&lt;/b> were found to be the most potent compounds against MAO-A (IC&lt;sub>50&lt;/sub> = 0.91 ± 0.15 nM) and MAO-B (IC&lt;sub>50&lt;/sub> = 0.84 ± 0.06 nM), while compound &lt;b>5c&lt;/b> showed t</pubmed_abstract><journal>Pharmaceuticals (Basel, Switzerland)</journal><pagination>11</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9865589</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and Evaluation of Novel &lt;i>S&lt;/i>-alkyl Phthalimide- and &lt;i>S&lt;/i>-benzyl-oxadiazole-quinoline Hybrids as Inhibitors of Monoamine Oxidase and Acetylcholinesterase.</pubmed_title><pmcid>PMC9865589</pmcid><pubmed_authors>Khan BA</pubmed_authors><pubmed_authors>Shawky AM</pubmed_authors><pubmed_authors>Iqbal J</pubmed_authors><pubmed_authors>Ibrahim MAA</pubmed_authors><pubmed_authors>Alqahtani AM</pubmed_authors><pubmed_authors>Gabr GA</pubmed_authors><pubmed_authors>Sidhom PA</pubmed_authors><pubmed_authors>Hamdani SS</pubmed_authors><pubmed_authors>Jalil S</pubmed_authors><pubmed_authors>Ejaz SA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and Evaluation of Novel &lt;i>S&lt;/i>-alkyl Phthalimide- and &lt;i>S&lt;/i>-benzyl-oxadiazole-quinoline Hybrids as Inhibitors of Monoamine Oxidase and Acetylcholinesterase.</name><description>New &lt;i>S&lt;/i>-alkyl phthalimide &lt;b>5a&lt;/b>-&lt;b>f&lt;/b> and &lt;i>S&lt;/i>-benzyl &lt;b>6a&lt;/b>-&lt;b>d&lt;/b> analogs of 5-(2-phenylquinolin-4-yl)-1,3,4-oxadiazole-2-thiol (&lt;b>4&lt;/b>) were prepared by reacting &lt;b>4&lt;/b> with &lt;i>N&lt;/i>-bromoalkylphthalimide and CF&lt;sub>3&lt;/sub>-substituted benzyl bromides in excellent yields. Spectroscopic techniques were employed to elucidate the structures of the synthesized molecules. The inhibition activity of newly synthesized molecules toward MAO-A, MAO-B, and AChE enzymes, was also assessed. All these compounds showed activity in the submicromolar range against all enzymes. Compounds &lt;b>5a&lt;/b> and &lt;b>5f&lt;/b> were found to be the most potent compounds against MAO-A (IC&lt;sub>50&lt;/sub> = 0.91 ± 0.15 nM) and MAO-B (IC&lt;sub>50&lt;/sub> = 0.84 ± 0.06 nM), while compound &lt;b>5c&lt;/b> showed t</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-04-08T14:07:41.009Z</modification><creation>2024-10-16T17:13:37.836Z</creation></dates><accession>S-EPMC9865589</accession><cross_references><pubmed>36678507</pubmed><doi>10.3390/ph16010011</doi></cross_references></HashMap>