Ä«½ºÅÙÅ©¸²(Ŭ·ÎÆ®¸®¸¶Á¹)  [Clotrimazole]  
                    
                 
               
              
                
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                                          ÃëÇÏ                   
                                          
                              (2021.07.01) 
                                          
                       
                     
                    
                     
                        
	    				   BIT ¾àÈ¿ºÐ·ù 
                        
                          ¿Ü¿ë Ç×Áø±ÕÁ¦ (Antifungals : Skin & Mucous Membrane)
                         
                     
                    
                    
                      
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                      265[±â»ý¼º ÇǺÎÁúȯ¿ëÁ¦                                             ] 
                     
                    
                      
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646201760[A13350881]  \0 ¿ø/1g(2007.06.01) (ÇöÀç¾à°¡) \40 ¿ø/1g(2001.09.28) (º¯°æÀü¾à°¡) 
                         
                        
						     
						     
                         
                      
                     
                       
                     
                     
                    
                       ATCÄÚµå 
                      Clotrimazole  / D01AC01 
                     
                    
                    
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                        [Proprietary Name Search _ ƯÇãµî·Ï¸í,»óÇ¥¸íÀ¸·Î °Ë»ö]  
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	          ÀüüÀӽŠ±â°£º°·Î ¿©·¯µî±ÞÀÌ Á¸ÀçÇÒ ¼ö ÀÖÀ¸¸ç °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ º¸¿©Áý´Ï´Ù. ´Ü, º¹ÇÕÁ¦ÀÇ °æ¿ì ¸ðµç º¹ÇÕÁ¦¼ººÐ¿¡ ´ëÇÑ ÀÓºÎÅõ¿©µî±ÞÀÌ Ç¥½ÃµÈ°ÍÀº Àý´ë ¾Æ´Ï¸ç Ç¥½ÃµÈ°ÍÁß¿¡ °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ ³ªÅ¸³³´Ï´Ù. 
	          
	         
	      
	       
	   
	  
	      
	   
	  
	    
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				         (clotrimazole topical )
				        
	   
	  
	  
	  
	     
	     
	     
	     
	     
	     
	   
	 
	
	  
	      
	      
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    Mechanism of Action 
    
      Clotrimazole¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Clotrimazole interacts with yeast 14-¥á demethylase, a cytochrome P-450 enzyme that converts lanosterol to ergosterol, an essential component of the membrane. In this way, clotrimazole inhibits ergosterol synthesis, resulting in increased cellular permeability. Clotrimazole may also inhibit endogenous respiration, interact with membrane phospholipids, inhibit the transformation of yeasts to mycelial forms and the uptake of purine, impair triglyceride and/or phospholipid biosynthesis, and inhibit the movement of calcium and potassium ions across the cell membrane by blocking the ion transport pathway known as the Gardos channel. 
     
   
  
   
    Pharmacology 
     
      Clotrimazole¿¡ ´ëÇÑ Pharmacology Á¤º¸  Clotrimazole, an imidazole derivative with a broad spectrum of antimycotic activity, inhibits biosynthesis of the sterol ergostol, an important component of fungal cell membranes. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane. Betamethasone and clotrimazole are used together to treat cutaneous tinea infections. In studies in fungal cultures, the minimum fungicidal concentration of clotrimazole caused leakage of intracellular phosphorous compounds into the ambient medium with concomitant breakdown of cellular nucleic acids, and accelerated potassium etflux. Both of these events began rapidly and extensively after addition of the drug to the cultures. The primary action of clotrimazole is against dividing and growing organisms. 
     
   
  
   
    Metabolism 
    
      Clotrimazole¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 11A1 (CYP11A1)Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 2D6 (CYP2D6) 
     
   
  
   
    Protein Binding 
    
      Clotrimazole¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  90% 
     
   
  
   
    Half-life 
    
      Clotrimazole¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  2 hours 
     
   
  
   
    Absorption 
    
      Clotrimazole¿¡ ´ëÇÑ Absorption Á¤º¸  Poorly and erratically absorbed orally, minimal vaginal or topical absorption. 
     
   
  
   
    Pharmacokinetics 
    
      ClotrimazoleÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
Èí¼ö : ¿Ü¿ë : Á¤»ó ÇǺθ¦ ÅëÇØ¼´Â °ÅÀÇ Èí¼öµÇÁö ¾Ê´Â´Ù.
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	    Troches : Ÿ¾× ³óµµ : 3½Ã°£ À̳»
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    Biotransformation 
    
      Clotrimazole¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic (metabolized to inactive metabolites) 
     
   
  
   
    Toxicity 
    
      Clotrimazole¿¡ ´ëÇÑ Toxicity Á¤º¸  Symptoms of overdose include erythema, stinging, blistering, peeling, edema, pruritus, urticaria, burning, and general irritation of the skin, and cramps. 
     
   
  
   
    Drug Interactions 
    
      Clotrimazole¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Clotrimazole¿¡ ´ëÇÑ Food Interaction Á¤º¸  Not Available 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Clotrimazole¿¡ ´ëÇÑ Description Á¤º¸  An imidazole derivative with a broad spectrum of antimycotic activity. It inhibits biosynthesis of the sterol ergostol, an important component of fungal cell membranes. Its action leads to increased membrane permeability and apparent disruption of enzyme systems bound to the membrane. [PubChem] 
     
   
  
   
    Dosage Form 
    
      Clotrimazole¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Cream	IntravaginalCream	Topical 
     
   
  
   
    Drug Category 
    
      Clotrimazole¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti-Infective Agents, LocalAntifungal AgentsGrowth Inhibitors 
     
   
  
   
    Smiles String Canonical 
    
      Clotrimazole¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  ClC1=CC=CC=C1C(N1C=CN=C1)(C1=CC=CC=C1)C1=CC=CC=C1 
     
   
  
   
    Smiles String Isomeric 
    
      Clotrimazole¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  ClC1=CC=CC=C1C(N1C=CN=C1)(C1=CC=CC=C1)C1=CC=CC=C1 
     
   
  
   
    InChI Identifier 
    
      Clotrimazole¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C22H17ClN2/c23-21-14-8-7-13-20(21)22(25-16-15-24-17-25,18-9-3-1-4-10-18)19-11-5-2-6-12-19/h1-17H 
     
   
  
   
    Chemical IUPAC Name 
    
      Clotrimazole¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  1-[(2-chlorophenyl)-di(phenyl)methyl]imidazole 
     
   
    
 
    
     
  
    
       
      
        
          
            
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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
 
  
                  
 
               
  
  
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