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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">AJPTR025400</article-id>
      <title-group>
        <article-title>Synthesis and In Vitro Antimicrobial Evaluation of Pyrazole Clubbed Quinoline</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Parikh</surname>
            <given-names>Kalpesh S</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Patel</surname>
            <given-names>Rakesh P</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Joshi</surname>
            <given-names>Deepkumar S</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
      </contrib-group>
      <aff id="aff1">Chemistry Department, Sheth M N Science College, Patan, Gujarat, India 384265</aff>
      <pub-date pub-type="epub" iso-8601-date="2012-10-01">
        <month>10</month>
        <day>01</day>
        <year>2012</year>
      </pub-date>
      <volume>2</volume>
      <issue>5</issue>
      <abstract>
        <p>In present study, a novel series of 6-bromo-2,7,8-trichloro-3-(3’-phenyl-4’,5’-dihydro-1H-pyrazol-5’-yl)quinoline(a-i). These novel synthesized entities were elicited by IR, 1H NMR, 13C NMR, C,H,N Analyzer and mass spectra. The entities produced in laboratory were screened with strains of bacteria and fungi like Staphylococcus aureus, Bacillus Megaterium, Proteus vulgaris, Escherichia coli, and Aspergillus niger respectively. Out of nine different entities synthesized five derivatives showed excellent antibacterial activity and rest of them showed moderate antimicrobial activity.</p>
      </abstract>
      <kwd-group kwd-group-type="author">
        <kwd>antifungal agents</kwd>
        <kwd>pyrazolines</kwd>
        <kwd>antibacterial agents</kwd>
        <kwd>chalcones</kwd>
      </kwd-group>
    </article-meta>
  </front>
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