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  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>American Journal of PharmTech Research</journal-title>
        <abbrev-journal-title abbrev-type="publisher">AJPTR</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2249-3387</issn>
      <publisher>
        <publisher-name>undefined</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">AJPTR33049</article-id>
      <title-group>
        <article-title>Synthesis and Antimicrobial Activity of Metal Chelates of 2-(8-Quinolinol-5-Yl)–Methyl Amino-5 -Phenyl-1, 3, 4-Thiadiazole Derivatives</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Patel</surname>
            <given-names>Divyesh K</given-names>
          </name>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Singh</surname>
            <given-names>Arun</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date pub-type="epub" iso-8601-date="2013-06-01">
        <month>06</month>
        <day>01</day>
        <year>2013</year>
      </pub-date>
      <volume>3</volume>
      <issue>3</issue>
      <abstract>
        <p>The novel metal chelates of 2-(8-quinolinol-5-yl)–methyl amino-5 -phenyl-1, 3, 4-thiadiazole (1) has been synthesized and their antimicrobial properties were evaluated. These compounds were synthesized by reaction of 2-(8-quinolinol-5-yl)–methyl amino-5 -phenyl-1, 3, 4-thiadiazole (1) with metal acetate and characterized using IR, 1H-NMR and elemental analysis. The synthesized compounds were screened for their in vitro antimicrobial activity against microorganism P. Expansum. B. Thiobromine, Nigras pora Sp. T. roseum, A. Niger, B. megaterium, S. aureus, P. aeruginosa and E. coli. All of the compounds are active against the microorganism in which some are exhibited moderate to good activity, whereas some were less active.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Metal chelates</kwd>
        <kwd>5-chloromethyl-8-quinolinol</kwd>
        <kwd>5-phenyl-1</kwd>
        <kwd>3</kwd>
        <kwd>4-thiadiazol-2-ylamine</kwd>
        <kwd>antifungal activity</kwd>
        <kwd>antibacterial activity</kwd>
      </kwd-group>
    </article-meta>
  </front>
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