Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer Agents

Several novel 6-aryl-5-cyano thiouracil derivatives were synthesized and explored for their activities as antibacterial, antifungal and anticancer agents. The antimicrobial evaluation revealed that compounds <strong>7b</strong> and <strong>7c</strong&...

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Main Authors: Sahar Mahmoud Abou-Seri, Azza Taher Taher
Format: Article
Language:English
Published: MDPI AG 2012-08-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/17/8/9868
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spelling doaj-ee5642d4c01b4517a4da627a67cdd4402020-11-24T22:56:47ZengMDPI AGMolecules1420-30492012-08-011789868988610.3390/molecules17089868Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer AgentsSahar Mahmoud Abou-SeriAzza Taher TaherSeveral novel 6-aryl-5-cyano thiouracil derivatives were synthesized and explored for their activities as antibacterial, antifungal and anticancer agents. The antimicrobial evaluation revealed that compounds <strong>7b</strong> and <strong>7c</strong> possessed superior antibacterial activity against the Gram positive bacteria <em>S. aureus</em> and <em>B. subtilis</em> compared to the reference drug amoxicillin. Moreover, compound <strong>4i</strong> was found to be a broad spectrum antimicrobial agent and it also exhibited the highest antifungal activity against <em>C. albicans</em>, even higher than the reference drug amphotericin B (MIC = 2.34, 3.00 μg/mL respectively). Selected compounds were tested for <em>in vitro</em> cytotoxicity at a single 10<sup>−5</sup> M concentration in accordance to the NCI (USA) protocol. The preliminary screening results showed that most of the compounds had limited cytotoxic activity against renal cancer UO-31 and/or A498 cell lines. Nevertheless, compounds <strong>6d</strong> and <strong>6i</strong> displayed potent growth inhibitory effect toward non-small cell lung cancer HOP-92 and leukemia MOLT-4 cell lines, respectively.http://www.mdpi.com/1420-3049/17/8/98686-aryl-5-cyano thiouracilsantibacterialantifungalanticancer
collection DOAJ
language English
format Article
sources DOAJ
author Sahar Mahmoud Abou-Seri
Azza Taher Taher
spellingShingle Sahar Mahmoud Abou-Seri
Azza Taher Taher
Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer Agents
Molecules
6-aryl-5-cyano thiouracils
antibacterial
antifungal
anticancer
author_facet Sahar Mahmoud Abou-Seri
Azza Taher Taher
author_sort Sahar Mahmoud Abou-Seri
title Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer Agents
title_short Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer Agents
title_full Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer Agents
title_fullStr Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer Agents
title_full_unstemmed Synthesis and Bioactivity Evaluation of New 6-Aryl-5-cyano Thiouracils as Potential Antimicrobial and Anticancer Agents
title_sort synthesis and bioactivity evaluation of new 6-aryl-5-cyano thiouracils as potential antimicrobial and anticancer agents
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2012-08-01
description Several novel 6-aryl-5-cyano thiouracil derivatives were synthesized and explored for their activities as antibacterial, antifungal and anticancer agents. The antimicrobial evaluation revealed that compounds <strong>7b</strong> and <strong>7c</strong> possessed superior antibacterial activity against the Gram positive bacteria <em>S. aureus</em> and <em>B. subtilis</em> compared to the reference drug amoxicillin. Moreover, compound <strong>4i</strong> was found to be a broad spectrum antimicrobial agent and it also exhibited the highest antifungal activity against <em>C. albicans</em>, even higher than the reference drug amphotericin B (MIC = 2.34, 3.00 μg/mL respectively). Selected compounds were tested for <em>in vitro</em> cytotoxicity at a single 10<sup>−5</sup> M concentration in accordance to the NCI (USA) protocol. The preliminary screening results showed that most of the compounds had limited cytotoxic activity against renal cancer UO-31 and/or A498 cell lines. Nevertheless, compounds <strong>6d</strong> and <strong>6i</strong> displayed potent growth inhibitory effect toward non-small cell lung cancer HOP-92 and leukemia MOLT-4 cell lines, respectively.
topic 6-aryl-5-cyano thiouracils
antibacterial
antifungal
anticancer
url http://www.mdpi.com/1420-3049/17/8/9868
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AT azzatahertaher synthesisandbioactivityevaluationofnew6aryl5cyanothiouracilsaspotentialantimicrobialandanticanceragents
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