<?xml version="1.0" encoding="UTF-8"?>



<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2017-12-25</publicationDate>
    
        <volume>14</volume>
        <issue>4</issue>

 
    <startPage>1449</startPage>
    <endPage>1456</endPage>

	 
      <doi>10.13005/bbra/2590</doi>
        <publisherRecordId>28484</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Molecular Docking Studies of Phytocompounds from Aloe Vera (L.) Burm. F. Having Anticancer Property, Against an Antiapoptotic Bcl-2 Protein</title>

    <authors>
	 


      <author>
       <name>Dhanya Narayanan Nair</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>S. Padmavathy</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Bioinformatics, Nirmala College for Women, Redfields, Coimbatore, Tamil Nadu-641018, India.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">B-cell lymphocyte-2 (Bcl-2) is an antiapoptotic protein, which is an important member of Bcl-2  family. The current study involves molecular docking of  six antineoplastic phytocompounds from <em>Aloe vera</em> (L.) Burm.f. against the protein Bcl-2. Docetaxel, a known inhibitor of Bcl-2 was used as a control in this study. All the studied phytocompounds bound within the same binding pocket as that of Docetaxel and thus can be considered as potential inhibitors of Bcl-2 protein. Among the six phytocompounds studied, AVG4 showed the best docking result, with a minimum pharmacological energy, -198.9 kcal/mol, followed by AVG6 and AVG3 as the second and third best phytocompound while AVL3 has the maximum pharmacological energy -103.8 kcal/mol. AVL3 is involved in cation-pi interactions with the Tyr9 residue of the Bcl-2 protein which is not considered while calculating pharmacological energy scoring function. Calculation of energy due to cation-pi interactions may result in the increase in total binding energy of AVL3, which may significantly increase the pharmacological energy, <em>E<sub>Pharma</sub></em> by approximately -8 kcal/mol, resulting in another potential anticancer phytocompound.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol14no4/molecular-docking-studies-of-phytocompounds-from-aloe-vera-l-burm-f-having-anticancer-property-against-an-antiapoptotic-bcl-2-protein/</fullTextUrl>



      <keywords language="eng">
        <keyword><em>Aloe vera</em>; Antiapoptotic; Anticancer; Bcl-2; <em>Aloe vera</em> leaf skin; AVL: AVG:<em>Aloe vera</em> gel; Asp: Asparagine; Asn: Asparagine; Ala: Alanine; Bcl-2: B-cell lymphoma-2;Gly: Glycine; Gln: Glutamine; His: Histidine;Ile: Isoleucine; Molecular Docking; Phytocompounds; Tyr: Tyrosine; Thr: Threonine;  Trp: Tryptophan;</keyword>
      </keywords>

  </record>
</records>