کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1397943 | 1501201 | 2009 | 6 صفحه PDF | دانلود رایگان |

Several 5-arylidene-4-thioxo-thiazolidine-2-ones (3a–n) were synthesized and evaluated as antimicrobial agents against representative strains, including multidrug-resistant strains of clinical isolates. Also, the antiproliferative activity was evaluated against two human carcinoma cell lines (NCI-H292 and HEp-2). The compounds containing the 5-arylidene subunit presented greater antimicrobial activities against Gram positive bacteria, including the multidrug-resistant clinical isolates, than the 4-thioxo-thiazolidine-2-one. Important SAR information was also gathered, such as the contribution of thiocarbonyl attached at 4-position on the thiazolidine heterocyclic for antimicrobial properties. None of the derivatives exhibited significant antiproliferative activity against the human carcinoma cell lines.
New antimicrobial structures: 5-arylidene-4-thioxo-thiazolidine-2-ones represent a compound class that are antimicrobial agents, and viewed with the capacity to inhibit the proliferation of representative strains, including multidrug-resistant isolates. Important SAR information was also gathered, and is different from previously reported SARs of this scaffold.Figure optionsDownload as PowerPoint slide
Journal: European Journal of Medicinal Chemistry - Volume 44, Issue 5, May 2009, Pages 2038–2043