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  <record>
    <language>eng</language>
    <publisher>Ansari Education and Research Society</publisher>
    <journalTitle>Journal of Ultra Chemistry</journalTitle>
    <issn>0973-3450</issn>
    <eissn>2319-8036</eissn>
    <publicationDate>December 2007</publicationDate>
    <volume>3</volume>
    <issue>1</issue>
    <startPage>1</startPage>
    <endPage>6</endPage>
    <doi>juc</doi>
    <publisherRecordId>779</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis of 4-thiazolidinone derivatives for potential antifungal activity</title>
    <authors>
      <author>
        <name>Anees A. Siddiqui,</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Aftab</name>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>M. Islam</name>
        <affiliationId>1</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Hamdard University, New Delhi - 110062 (INDIA)</affiliationName>
    </affiliationsList>
    <abstract language="eng">&lt;p style="text-align: justify;"&gt;The final 4-thiazolidinone derivatives (4a-r) were synthesized from methyl acrylate/methmethyl acrylate and studied in vitro for antifungal activity against &lt;em&gt;A. niger, C. albicans, A. flavus, T. rubrum, A. fumigatus&lt;/em&gt; and &lt;em&gt;P. citrinium&lt;/em&gt; at the concentration of 40, 80 and 160 &amp;micro;g/ml. These compounds showed good antifungal activity. Compound 4a with p-chloro substitution at both the phenyl ring showed activity even better than the used standard drug, Voriconazole.&lt;/p&gt;&#xD;
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</abstract>
    <fullTextUrl format="html">https://journalofchemistry.org/paper/779/</fullTextUrl>
    <keywords>
      <keyword language="eng">antifungal activity</keyword>
    </keywords>
    <keywords>
      <keyword language="eng">thiazolidinone</keyword>
    </keywords>
  </record>
</records>
