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  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2024-06-25</publicationDate>
    
        <volume>17</volume>
        <issue>2</issue>

 
    <startPage>1103</startPage>
    <endPage>1114</endPage>

	 
      <doi>10.13005/bpj/2926</doi>
        <publisherRecordId>57840</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Screening of Phosphoinositide-3 Kinase Inhibitors from Argemone mexicana Leaves</title>

    <authors>
	 


      <author>
       <name>Sowmya Priya Manoharan</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Sangilimuthu Alagar Yadav</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Gnanaselvan Suvathika</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Priyadharshini  Anandhan</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	 


      <author>
       <name>Balamurugan Pandiyan</name>

		
	<affiliationId>1</affiliationId>
      </author>
    


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Biotechnology, Karpagam Academy of Higher Education, Coimbatore, Tamil Nadu.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">Background: Phosphoinositide 3 kinase belongs to the enzyme family which is responsible for the development of cellular trafficking and uncontrolled cellular division which in turn to cancer metastasis. Activation of the PI3k-Akt-mTOR pathway tends to promote oncogenesis in Lung Cancer and its mutation leads to resistance in EGFR tyrosine kinase inhibitors. Objective: Inhibition of the initial PI3k receptor through natural bioactive phytocompounds from <em>Argemone mexicana</em> that may prevent the side effects caused by the synthetic medication and improve the patient's life quality as natural medicine. Method: According to the previous research we did the Bioactive phytochemical screening from the methanol extract (AME) and powder (AMP) of <em>A. mexicana</em> leaf by analysing the GC-MS (Agilent), UPLC-QTOF-ESI-MS (Waters India Pvt Limited). Analyzed phytochemicals from the studies were subjected to molecular docking analysis using SeeSAR 9.2 software against PI3K (PDP ID: 4FA6) receptor. Result: GC-MS revealed 40 compounds including Cryptopine (17.5), beta-sitosterol (9.57), and Protopine (8.6) were found as major compounds. LC-MS analysis showed the presence of major compounds with 13 elements compared to the literature survey in both positive and negative ESI ranges. 29 compounds from the GC-MS and LC-MS were selected for analyzing the interaction between the cancer receptor-ligand complex according to the binding strategy. Conclusion: Phytoconstituents such as Galactitol, Succinic acid and N-feruloyltryamine from <em>A. mexicana</em> showed good binding affinity range and maximised hydrogen bonding that may assure possessing anticancer effect by controlling the PI3K pathway. This study would lead a major role in the preliminary screening of Drug Targets against the PI3K receptor.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol17no2/screening-of-phosphoinositide-3-kinase-inhibitors-from-argemone-mexicana-leaves/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Argemone mexicana</keyword>
      

      
        <keyword> GC-MS</keyword>
      

      
        <keyword> Lung Cancer</keyword>
      

      
        <keyword> Molecular docking</keyword>
      

      
        <keyword> PI3Kreceptor</keyword>
      

      
        <keyword> UPLC-Q-TOF-MS</keyword>
      
</keywords>
  </record>
</records>