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      °í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
      
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    Mechanism of Action 
    
      Terbinafine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Terbinafine is hypothesized to act by inhibiting squalene epoxidase, thus blocking the biosynthesis of ergosterol, an essential component of fungal cell membranes. 
     
   
  
   
    Pharmacology 
     
      Terbinafine¿¡ ´ëÇÑ Pharmacology Á¤º¸  Terbinafine is an allylamine antifungal agent and acts by inhibiting squalene epoxidase, thus blocking the biosynthesis of ergosterol, an essential component of fungal cell membranes. in vitro , mammalian squalene epoxidase is only inhibited at higher (4000 fold) concentrations than is needed for inhibition of the dermatophyte enzyme. Depending on the concentration of the drug and the fungal species test in vitro , Terbinafine may be fungicidal. However, the clinical significance of in vitro  data is unknown. 
     
   
  
   
    Metabolism 
    
      Terbinafine¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2D6 (CYP2D6) 
     
   
  
   
    Protein Binding 
    
      Terbinafine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  >99% 
     
   
  
   
    Half-life 
    
      Terbinafine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  36 hours 
     
   
  
   
    Absorption 
    
      Terbinafine¿¡ ´ëÇÑ Absorption Á¤º¸  Readily absorbed from gastrointestinal tract. 
     
   
  
   
    Pharmacokinetics 
    
      Terbinafine HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
Èí¼ö : ¿Ü¿ë : °ÅÀÇ Èí¼öµÇÁö ¾Ê´Â´Ù. 
 ¼Ò½Ç : Èí¼öµÈ ¾çÀÇ 75%±îÁö ½Å¹è¼³µÈ´Ù. Åõ¿©·®ÀÇ 3.5%°¡ ¿ä¿Í º¯À¸·Î ¹è¼³µÈ´Ù.  
 
	 
	
     
   
  
   
    Biotransformation 
    
      Terbinafine¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic 
     
   
  
   
    Toxicity 
    
      Terbinafine¿¡ ´ëÇÑ Toxicity Á¤º¸  Not Available 
     
   
  
   
    Drug Interactions 
    
      Terbinafine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Terbinafine¿¡ ´ëÇÑ Description Á¤º¸  Terbinafine hydrochloride (Lamisil) is a synthetic allylamine antifungal. It is highly lipophilic in nature and tends to accumulate in skin, nails, and fatty tissues. Like other allylamines, terbinafine inhibits ergosterol synthesis by inhibiting the fungal squalene epoxidase, an enzyme that is part of the fungal cell wall synthesis pathway. 
     
   
  
   
    Drug Category 
    
      Terbinafine¿¡ ´ëÇÑ Drug_Category Á¤º¸  AllylaminesAntifungal AgentsAntifungalsEnzyme InhibitorsTrypanocidal Agents 
     
   
  
   
    Smiles String Canonical 
    
      Terbinafine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CN(CC=CC 
     
   
  
   
    Smiles String Isomeric 
    
      Terbinafine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CN(C\C=C\C 
     
   
  
   
    InChI Identifier 
    
      Terbinafine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C21H25N/c1-21(2,3)15-8-5-9-16-22(4)17-19-13-10-12-18-11-6-7-14-20(18)19/h5-7,9-14H,16-17H2,1-4H3 
     
   
  
   
    Chemical IUPAC Name 
    
      Terbinafine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  N,6,6-trimethyl-N-(naphthalen-1-ylmethyl)hept-2-en-4-yn-1-amine 
     
   
    
 
    
     
  
    
       
      
        
          
            
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2025-11-03
               
              
                
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  The database contains the following fields:
The generic name of each chemical
For module A10 (liver enzyme composite module):
Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method)
Number of endpoints at which each compound is marginally active (M)
Number of endpoints at which each compound is active (A)
For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively):
Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method)
Number of ADR reports for each compound, given as <4 or ¡Ã4
Reporting Index value for each compound, except where no shipping units were available (NSU)
Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period.
TERBINAFINE [GGT Increase] [Composite Activity] (Score)   I  (Marginal)   1 (Active)   0 [Alkaline Phosphatase Increase] (Activity Score)   I  (Number of Rpts)   ¡Ã4 (Index value)   1.1 [SGOT Increase] (Activity Score)   M  (Number of Rpts)   ¡Ã4 (Index value)   3.1 [SGPT Increase] (Activity Score)   I  (Number of Rpts)   ¡Ã4 (Index value)   2.8 [LDH Increase] (Activity Score)   I  (Number of Rpts)   ¡Ã4 (Index value)   1.1 [GGT Increase] (Activity Score)   I  (Number of Rpts)   ¡Ã4 (Index value)   2.6 
 
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