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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2015-01-20</publicationDate>
    
        <volume>1</volume>
        <issue>1</issue>

 
    <startPage>195</startPage>
    <endPage>200</endPage>

	    <publisherRecordId>306</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis and Antimicrobial Activity of some Quinazolinone Derivatives</title>

    <authors>
	 


      <author>
       <name>Ambuj Singh</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>S. K. Prajapati</name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	 


      <author>
       <name>K. P. Namdeo</name>

		
	<affiliationId>2</affiliationId>
      </author>
    

	 


      <author>
       <name>V. K. Singh</name>

		
	<affiliationId>2</affiliationId>
      </author>
    


	 


      <author>
       <name>S. K. Verma</name>

		
	<affiliationId>2</affiliationId>
      </author>
    


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Institute of Pharmacy, Bundelkhand University, Jhansi </affiliationName>
    

		
		<affiliationName affiliationId="2">S. L. T. Institute of Pharmaceutical Sciences, G.G.U., Bilaspur, Chhatisgarh</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Synthesis of six 2,3,6-trisubstituted Quinazolin-4-one is reported. All six compounds contain a bromine atom at position 6, phenylimino thiazolidinone group at position 2 and 3 different derivatives has been synthesized by changing X (A-1: benzaldehyde, A-2: m-chlorobenzaldehyde, A-3: o-hydroxybenzaldehyde, A-4: p-methoxybenzaldehyde, A-5: o-nitrobenzaldehyde, A-6: m-nitrobenzaldehyde). All the synthesized compounds work evaluated for their antimicrobial (against two gram positive and two gram negative microorganism) and antifungal activity (against A. niger and C. albicans).</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol1no1/synthesis-and-antimicrobial-activity-of-some-quinazolinone-derivatives/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Antimicrobial activity</keyword>
      

      
        <keyword> Quinazolinone derivatives</keyword>
      
</keywords>
  </record>
</records>