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    Mechanism of Action 
    
      Albendazole¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Albendazole causes degenerative alterations in the tegument and intestinal cells of the worm by binding to the colchicine-sensitive site of tubulin, thus inhibiting its polymerization or assembly into microtubules. The loss of the cytoplasmic microtubules leads to impaired uptake of glucose by the larval and adult stages of the susceptible parasites, and depletes their glycogen stores. Degenerative changes in the endoplasmic reticulum, the mitochondria of the germinal layer, and the subsequent release of lysosomes result in decreased production of adenosine triphosphate (ATP), which is the energy required for the survival of the helminth. Due to diminished energy production, the parasite is immobilized and eventually dies. 
     
   
  
   
    Pharmacology 
     
      Albendazole¿¡ ´ëÇÑ Pharmacology Á¤º¸  Albendazole is a broad-spectrum anthelmintic. The principal mode of action for albendazole is by its inhibitory effect on tubulin polymerization which results in the loss of cytoplasmic microtubules. 
     
   
  
   
    Metabolism 
    
      Albendazole¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
     
   
  
   
    Protein Binding 
    
      Albendazole¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  70% bound to plasma protein 
     
   
  
   
    Half-life 
    
      Albendazole¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  Terminal elimination half-life ranges from 8 to 12 hours (single dose, 400mg). 
     
   
  
   
    Absorption 
    
      Albendazole¿¡ ´ëÇÑ Absorption Á¤º¸  Poorly absorbed from the gastrointestinal tract due to its low aqueous solubility. Oral bioavailability appears to be enhanced when coadministered with a fatty meal (estimated fat content 40 g) 
     
   
  
   
    Pharmacokinetics 
    
      AlbendazoleÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
Èí¼ö : °ÅÀÇ Èí¼öµÇÁö ¾Ê´Â´Ù. Áö¹æ½ÄÀÌ¿Í °°ÀÌ º¹¿ëÇϸé Èí¼ö°¡ Áõ°¡µÈ´Ù. 
 ´Ü¹é°áÇÕ : 70% 
 ´ë»ç : ´ëºÎºÐ °£´ë»çµÈ´Ù. 
 ¹Ý°¨±â : 8.5 ½Ã°£ 
  
     
   
  
   
    Biotransformation 
    
      Albendazole¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic. Rapidly converted in the liver to the primary metabolite, albendazole sulfoxide, which is further metabolized to albendazole sulfone and other primary oxidative metabolites that have been identified in human urine. 
     
   
  
   
    Toxicity 
    
      Albendazole¿¡ ´ëÇÑ Toxicity Á¤º¸  Symptoms of overdose include elevated liver enzymes, headaches, hair loss, low levels of white blood cells (neutropenia), fever, and itching. 
     
   
  
   
    Drug Interactions 
    
      Albendazole¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Albendazole¿¡ ´ëÇÑ Description Á¤º¸  A benzimidazole broad-spectrum anthelmintic structurally related to mebendazole that is effective against many diseases. (From Martindale, The Extra Pharmacopoeia, 30th ed, p38) 
     
   
  
   
    Drug Category 
    
      Albendazole¿¡ ´ëÇÑ Drug_Category Á¤º¸  AnthelminticsAnticestodal AgentsAntiprotozoal AgentsTubulin Modulators 
     
   
  
   
    Smiles String Canonical 
    
      Albendazole¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CCCSC1=CC2=C(C=C1)N=C(NC(=O)OC)N2 
     
   
  
   
    Smiles String Isomeric 
    
      Albendazole¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CCCSC1=CC2=C(C=C1)N=C(NC(=O)OC)N2 
     
   
  
   
    InChI Identifier 
    
      Albendazole¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C12H15N3O2S/c1-3-6-18-8-4-5-9-10(7-8)14-11(13-9)15-12(16)17-2/h4-5,7H,3,6H2,1-2H3,(H2,13,14,15,16)/f/h14-15H 
     
   
  
   
    Chemical IUPAC Name 
    
      Albendazole¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  methyl N-(6-propylsulfanyl-1H-benzimidazol-2-yl)carbamate 
     
   
    
 
    
     
  
    
       
      
        
          
            
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