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    <registrant>UJPR</registrant>
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      <journal_metadata>
        <full_title>Universal Journal of Pharmaceutical Research</full_title>
        <abbrev_title>Univ J Pharm Res</abbrev_title>
        <issn media_type="electronic">2456-8058</issn>
      </journal_metadata>
      <journal_issue>
        <publication_date media_type="online">
          <month>04</month>
          <day>11</day>
          <year>2018</year>
        </publication_date>
      </journal_issue>
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        <titles>
          <title>SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL IMIDAZOLE BASED COMPOUNDS</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <given_name>Bipin Kumar</given_name>
            <surname>Verma</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Sunil</given_name>
            <surname>Kapoor</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Umesh</given_name>
            <surname>Kumar</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Savita</given_name>
            <surname>Pandey</surname>
          </person_name>
          <person_name contributor_role="author" sequence="first">
            <given_name>Priti</given_name>
            <surname>Arya</surname>
          </person_name>
        </contributors>
        <jats:abstract xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1">
          <jats:p>Some new imidazole derivatives (3i-xii) were synthesized as per design synthetic protocol scheme. The structures of newly prepared compounds were confirmed by modern analytical technique and elemental analysis. All the synthetic compounds were screened for their antimicrobial activity against bacterial results showed good to remarkable activity. The MIC (minimum inhibitory concentration) values were determined by comparison to ciprofloxacin (anti-bacterial) and fluconazole (anti-fungal) as standard drug. Among them, compound 3iv and 3x exhibited notable antimicrobial activity. These compounds may be used as new template for the searching of potential antimicrobial agents.&#13;
Google Scholar</jats:p>
        </jats:abstract>
        <publication_date media_type="online">
          <month>01</month>
          <day>01</day>
          <year>2017</year>
        </publication_date>
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          <doi>10.22270/ujpr.v2i1.R5</doi>
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