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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">AJPTR44042</article-id>
      <title-group>
        <article-title>Anthelmintic and Anti-Bacterial Studies of Synthesized Azetidinones Derivatives of Quinazolinones</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Kandpal</surname>
            <given-names>Bhavna</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Meshram</surname>
            <given-names>Jyotsna</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Shaikh</surname>
            <given-names>Ambareen</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
      </contrib-group>
      <aff id="aff1">Department of chemistry, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur, Maharashtra, India.</aff>
      <pub-date pub-type="epub" iso-8601-date="2014-08-01">
        <month>08</month>
        <day>01</day>
        <year>2014</year>
      </pub-date>
      <volume>4</volume>
      <issue>4</issue>
      <abstract>
        <p>The present work deals with the synthesis of azetidinone derivatives of quinazolinones and  the structures of the compounds obtained have been established based on spectral (IR, 1H NMR,13C NMR and Mass) data. The present study also involves in vitro anthelmintic and antibacterial activity of the synthesized derivatives a few strains (gram positive and gram negative) of bacteria. All the compounds showed against moderate to satisfactory activities.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>Azetidinones</kwd>
        <kwd>Quinazolinones</kwd>
        <kwd>Anthelmintic</kwd>
        <kwd>Antibacterial.</kwd>
      </kwd-group>
    </article-meta>
  </front>
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