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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>2026-09-30</publicationDate>
    
        <volume>19</volume>
        <issue>3</issue>

 
    <startPage>2610</startPage>
    <endPage>2621</endPage>

	 
      <doi>10.13005/bpj/3519</doi>
        <publisherRecordId>73237</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Cytotoxic Constituents from the Stem Bark and Leaves of Cinnamomum Bejolghota: Isolation, Structure Elucidation, and Molecular Docking Studies</title>

    <authors>
	 


      <author>
       <name>Le Thi Phuong</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Lam Hoang</name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	 


      <author>
       <name>Nguyen Duc Hieu</name>

		
	<affiliationId>3</affiliationId>
      </author>
    

	 


      <author>
       <name>Do Dang Truc An</name>

		
	<affiliationId>4</affiliationId>
      </author>
    


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Vietnam Academy of Science and Technology, Hanoi, 10000, Vietnam</affiliationName>
    

		
		<affiliationName affiliationId="2">University of California Santa Cruz, Santa Cruz, CA, 95064, USA</affiliationName>
    
		
		<affiliationName affiliationId="3">Edulight Education - Communication Joint Stock Company, Hanoi, 10000, Vietnam</affiliationName>
    
		
		<affiliationName affiliationId="4">Hanoi - Amsterdam High School for the Gifted, Hanoi, 10000, Vietnam</affiliationName>
    
		
		
	  </affiliationsList>






    <abstract language="eng">The genus <em>Cinnamomum</em> (Lauraceae) is a rich source of bioactive metabolites, yet the Vietnamese species <em>Cinnamomum bejolghota</em> remains incompletely characterised. This study aimed to characterise the constituents of the stem bark and leaves of <em>C. bejolghota</em>, evaluate their cytotoxicity, and explore their molecular targets by docking. Compounds were isolated by chromatographic methods and identified by spectroscopic analysis. Cytotoxicity was assessed against KB, HepG2, MCF-7 and SK-LU-1 cell lines using the MTT assay. Molecular docking against five protein targets and <em>in silico</em> ADME profiling were performed. Sixteen compounds were obtained, including the steroid ergosta-4,6,8(14),22-tetraen-3-one and the flavonol glycoside afzelin, both reported for the first time in this species. Of the 16 compounds, 14 had been reported by our group in two preliminary communications; only the steroid and the flavonol glycoside are newly described from this species. The bis(dimethoxyphenyl)pyridine alkaloid showed moderate cytotoxicity (IC<sub>50</sub> 31.1 to 45.9 µM), whereas the steroid was weakly active. Docking indicated that the active alkaloid bound topoisomerase IIα and tubulin more strongly than its inactive analogue, and the β-carboline alkaloid bound monoamine oxidase A as strongly as harmine. <em>C. bejolghota</em> produces a structurally diverse set of metabolites; the integrated cytotoxicity, docking and ADME data provide a rationale for the observed bioactivities and candidates for further study.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol19no3/cytotoxic-constituents-from-the-stem-bark-and-leaves-of-cinnamomum-bejolghota-isolation-structure-elucidation-and-molecular-docking-studies/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Alkaloids</keyword>
      

      
        <keyword> Cinnamomum bejolghota</keyword>
      

      
        <keyword> Cytotoxicity</keyword>
      

      
        <keyword> Molecular docking</keyword>
      

      
        <keyword> Phytochemistry</keyword>
      
</keywords>
  </record>
</records>