<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(19)</volume><submitter>Barmak A</submitter><funding>Research Council, Persian Gulf University</funding><pubmed_abstract>A series of new quinazoline derivatives were designed and synthesized via a one-pot condensation reaction between isatoic anhydride and aromatic aldehydes with anilines using aluminum sulfate as a catalyst in refluxing ethanol. Their structures were confirmed by their physical, IR, &lt;sup>1&lt;/sup>H NMR, &lt;sup>13&lt;/sup>C NMR, and mass spectroscopy data and evaluated for some biological effects, including the antioxidant and α-glucosidase inhibitory activities as well as some in vivo hematological parameters. The ability of synthesized compounds in the inhibition of α-glucosidase was also investigated through the in silico study. The significant and important changes in some hematological tests were perceived. Notably, compound &lt;b>4h&lt;/b> showed more reducing effects on cholesterol and triglycerid</pubmed_abstract><journal>ACS omega</journal><pagination>18087-18099</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6843711</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis, Structural Studies, and α-Glucosidase Inhibitory, Antidiabetic, and Antioxidant Activities of 2,3-Dihydroquinazolin-4(1&lt;i>H&lt;/i>)-ones Derived from Pyrazol-4-carbaldehyde and Anilines.</pubmed_title><pmcid>PMC6843711</pmcid><pubmed_authors>Barmak A</pubmed_authors><pubmed_authors>Niknam K</pubmed_authors><pubmed_authors>Mohebbi G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis, Structural Studies, and α-Glucosidase Inhibitory, Antidiabetic, and Antioxidant Activities of 2,3-Dihydroquinazolin-4(1&lt;i>H&lt;/i>)-ones Derived from Pyrazol-4-carbaldehyde and Anilines.</name><description>A series of new quinazoline derivatives were designed and synthesized via a one-pot condensation reaction between isatoic anhydride and aromatic aldehydes with anilines using aluminum sulfate as a catalyst in refluxing ethanol. Their structures were confirmed by their physical, IR, &lt;sup>1&lt;/sup>H NMR, &lt;sup>13&lt;/sup>C NMR, and mass spectroscopy data and evaluated for some biological effects, including the antioxidant and α-glucosidase inhibitory activities as well as some in vivo hematological parameters. The ability of synthesized compounds in the inhibition of α-glucosidase was also investigated through the in silico study. The significant and important changes in some hematological tests were perceived. Notably, compound &lt;b>4h&lt;/b> showed more reducing effects on cholesterol and triglycerid</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2025-04-21T20:38:45.263Z</modification><creation>2020-05-21T18:35:45Z</creation></dates><accession>S-EPMC6843711</accession><cross_references><pubmed>31720511</pubmed><doi>10.1021/acsomega.9b01906</doi></cross_references></HashMap>