Synthesis, crystal structure and evaluation of the cytotoxic, antimicrobial activity of some S- and N-derivatives of 5-phenyl-1,2,4-triazole-2,4-dihydro-3-thione
{"title":"Synthesis, crystal structure and evaluation of the cytotoxic, antimicrobial activity of some S- and N-derivatives of 5-phenyl-1,2,4-triazole-2,4-dihydro-3-thione","authors":"Abdukhakim Ziyaev , Sobirdjan Sasmakov , Rasul Okmanov , Utkir Makhmudov , Turdibek Toshmurodov , Мavluda Ziyaeva , Nigora Tosheva , Shakhnoz Azimova","doi":"10.1016/j.cdc.2025.101182","DOIUrl":null,"url":null,"abstract":"<div><div>In this work, we report the synthesis of several <em>S</em>- and <em>N</em>-derivatives of 5-phenyl-1,2,4-triazole-2,4-dihydro-3-thione (<strong>3</strong>–<strong>6</strong>). Methods for the preparation of these compounds were based on the alkylation and aminomethylation reactions of triazolethione (<strong>2</strong>). The target products were obtained in high (85–98%) yield. The structures of the synthesized compounds were confirmed by IR, <sup>1</sup>H and <sup>13</sup>C NMR spectroscopy, mass spectrometry, and selective X-ray diffraction analysis. All compounds were tested in vitro against four human cancer cells <em>(HeLa, HBL-100, HEp-2, CCRF-CEM),</em> gram-positive <em>(Staphylococcus aureus, Bacillus subtilis)</em> and gram-negative bacteria <em>(Escherichia coli, Pseudomonas aeruginosa),</em> as well as the opportunistic fungus <em>Candida albicans.</em></div></div>","PeriodicalId":269,"journal":{"name":"Chemical Data Collections","volume":"56 ","pages":"Article 101182"},"PeriodicalIF":2.2180,"publicationDate":"2025-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Data Collections","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405830025000047","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Chemistry","Score":null,"Total":0}
引用次数: 0
Abstract
In this work, we report the synthesis of several S- and N-derivatives of 5-phenyl-1,2,4-triazole-2,4-dihydro-3-thione (3–6). Methods for the preparation of these compounds were based on the alkylation and aminomethylation reactions of triazolethione (2). The target products were obtained in high (85–98%) yield. The structures of the synthesized compounds were confirmed by IR, 1H and 13C NMR spectroscopy, mass spectrometry, and selective X-ray diffraction analysis. All compounds were tested in vitro against four human cancer cells (HeLa, HBL-100, HEp-2, CCRF-CEM), gram-positive (Staphylococcus aureus, Bacillus subtilis) and gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa), as well as the opportunistic fungus Candida albicans.
期刊介绍:
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