{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,4]],"date-time":"2026-02-04T20:40:38Z","timestamp":1770237638070,"version":"3.49.0"},"reference-count":52,"publisher":"Walter de Gruyter GmbH","issue":"11-12","funder":[{"DOI":"10.13039\/king","name":"King Saud University, Riyadh, Saudi Arabia","doi-asserted-by":"publisher","award":["RSP2025R388"],"award-info":[{"award-number":["RSP2025R388"]}],"id":[{"id":"10.13039\/king","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,11,25]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Alzheimer\u2019s disease is a serious neurological disorder, and traditional therapies for Alzheimer\u2019s, like radiation and surgical procedures, as well as chemotherapeutics, are usually linked with multiple negative consequences. Finding a novel therapeutic anti-Alzheimer agent with high efficacy and minimal side effects, we have designed and synthesized benzothiazolidinone-derived thiadiazole-based Schiff base derivatives (\n                    <jats:bold>1\u201315<\/jats:bold>\n                    ). Biological assessment of these compounds was carried out against acetylcholinesterase and butyrylcholinesterase, and all the derivatives showed varying degrees of inhibitory activity. Analog\n                    <jats:bold>8<\/jats:bold>\n                    (IC\n                    <jats:sub>50<\/jats:sub>\n                    \u00a0=\u00a0\n                    <jats:bold>3.60\u00a0\u00b1\u00a00.20<\/jats:bold>\n                    and\n                    <jats:bold>4.10\u00a0\u00b1\u00a00.20\u202f\u03bcM<\/jats:bold>\n                    for acetylcholinesterase and butyrylcholinesterase, respectively) demonstrated spellbinding efficacy in contrast to standard donepezil (IC\n                    <jats:sub>50<\/jats:sub>\n                    \u00a0=\u00a0\n                    <jats:bold>50\u00a0\u00b1\u00a00.10<\/jats:bold>\n                    and\n                    <jats:bold>8.10\u00a0\u00b1\u00a00.20\u202f\u03bcM<\/jats:bold>\n                    ). The surpassing inhibition of analog\n                    <jats:bold>8<\/jats:bold>\n                    is due to highly reactive CF\n                    <jats:sub>3<\/jats:sub>\n                    moiety at the\n                    <jats:italic>para<\/jats:italic>\n                    -position, inhibiting the enzymes via strong hydrogen bond. Analog\n                    <jats:bold>7<\/jats:bold>\n                    with IC\n                    <jats:sub>50<\/jats:sub>\n                    value of\n                    <jats:bold>5.70\u00a0\u00b1\u00a00.10<\/jats:bold>\n                    and\n                    <jats:bold>6.20\u00a0\u00b1\u00a00.40\u202f\u03bcM<\/jats:bold>\n                    was also found with strong therapeutic potential than standard drug. The strong inhibition potential of lead compounds was also evaluated under enzyme kinetics and spellbinding potential was observed. Biological effectiveness of potent compounds was validated by visualizing the binding interactions via\n                    <jats:italic>in silico<\/jats:italic>\n                    molecular docking study and prediction of drug-likeness via ADME analysis. All the synthesized compounds were analyzed for their structural confirmation via\n                    <jats:sup>1<\/jats:sup>\n                    HNMR,\n                    <jats:sup>13<\/jats:sup>\n                    CNMR, and HREI-MS.\n                  <\/jats:p>","DOI":"10.1515\/znc-2024-0243","type":"journal-article","created":{"date-parts":[[2025,3,21]],"date-time":"2025-03-21T02:49:15Z","timestamp":1742525355000},"page":"727-750","source":"Crossref","is-referenced-by-count":1,"title":["Insight the confirmation of benzothiazolidinone-derived thiadiazole scaffolds as promising antiurease and anti-Alzheimer agents: synthesis,\n                    <i>in\u00a0vitro<\/i>\n                    , and\n                    <i>in silico<\/i>\n                    investigations"],"prefix":"10.1515","volume":"80","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5404-0954","authenticated-orcid":false,"given":"Shoaib","family":"Khan","sequence":"first","affiliation":[{"name":"Department of Chemistry , 469633 Abbottabad University of Science and Technology , Abbottabad 22500 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tayyiaba","family":"Iqbal","sequence":"additional","affiliation":[{"name":"Department of Chemistry , 469633 Abbottabad University of Science and Technology , Abbottabad 22500 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tayyaba","family":"Zahoor","sequence":"additional","affiliation":[{"name":"Department of Chemistry , 469633 Abbottabad University of Science and Technology , Abbottabad 22500 , Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1945-681X","authenticated-orcid":false,"given":"Rafaqat","family":"Hussain","sequence":"additional","affiliation":[{"name":"College of Biology , Hunan University Changsha , Hunan 410082 , P.R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4612-5875","authenticated-orcid":false,"given":"Mohammad Shahidul","family":"Islam","sequence":"additional","affiliation":[{"name":"Department of Chemistry, College of Science , King Saud University , P.O. Box\u00a02455 , Riyadh 11451 , Saudi\u00a0Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kholood A.","family":"Dahlous","sequence":"additional","affiliation":[{"name":"Department of Chemistry, College of Science , King Saud University , P.O. Box\u00a02455 , Riyadh 11451 , Saudi\u00a0Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","published-online":{"date-parts":[[2025,3,21]]},"reference":[{"key":"2025110310023741153_j_znc-2024-0243_ref_001","doi-asserted-by":"crossref","unstructured":"Abid, O-U-R, Babar, TM, Ali, FI, Ahmed, S, Wadood, A, Rama, NH, et al.. 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