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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>2015-01-22</publicationDate>
    
        <volume>1</volume>
        <issue>2</issue>

 
    <startPage>257</startPage>
    <endPage>264</endPage>

	    <publisherRecordId>2429</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Synthesis of penicillin derivatives and study of their biological antibacterial activities</title>

    <authors>
	 


      <author>
       <name>Lakhdar Sekhri</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Mohammed Lazhar Kadri</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Choula Samira </name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Moussa Senigra</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Chemistry, Faculty of Sciences, University of Kasdi Merbah, Ouargla</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">The novel penicillin derivatives Amp-1 and Amx-1 have been synthesised via diazotising aniline with sodium nitrite in a medium of hydrochloric acid and the resulting phenyldiazonium chloride couples to ampicillin and amoxicillin. Esterification of ampicillin and amoxicillin with ethanol and isopropanol yielded the penicillin derivatives Amp-2, Amp-3, Amx-2, and Amx-3. The penicillin derivative Oxa-1 was successfully synthesized by nitration of oxacillin. These penicillin derivatives (except Oxa-1) showed significant activity against all the bacteria tested, Escherichia Coli, Streptococcus pneumonia, Protius, Staphylococcus aureus and Pseudomonas.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol1no2/synthesis-of-penicillin-derivatives-and-study-of-their-biological-antibacterial-activities/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Penicilin derivatives Amp-1</keyword>
      

      
        <keyword> Amx-1</keyword>
      

      
        <keyword> Antibacterial activity</keyword>
      
</keywords>
  </record>
</records>