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    Drugs By Indication 
    
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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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	          »ó±â ÀÓºÎÅõ¿©¿¡ ´ëÇÑ Á¤º¸´Â Àü»êó¸® µÇ¸é¼ ÀÔ·Â ¿À·ù °¡´É¼ºÀÌ Á¸ÀçÇÕ´Ï´Ù. ¿À·ù °¡´É¼ºÀ» ÃÖ¼ÒÈÇϱâ À§ÇÏ¿© ¸¹Àº ³ë·ÂÀ» ±â¿ïÀ̰í ÀÖÀ¸³ª, ±× Á¤È®¼º¿¡ ´ëÇÏ¿© È®½ÅÀ» µå¸± ¼ö ¾ø½À´Ï´Ù. ÀÌ¿¡ ´ëÇØ ȸ»ç´Â Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. 
	         
	         
	      
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	          ¹Ýµå½Ã °ø½Å·Â ÀÖ´Â ¹®ÇåÀ» ´Ù½Ã Çѹø Âü°í  ÇϽñ⠹ٶó¸ç ÀÇ»ç ¶Ç´Â ¾à»çÀÇ ÆÇ´Ü¿¡ µû¶ó Åõ¿©¿©ºÎ°¡ °áÁ¤µÇ¾î¾ß ÇÕ´Ï´Ù. 
	         
	         
	      
	   
	 
      
     
   
  
  
  	   
  
  	   
  
  	   
  
  
     
      Pharmacokinetics 
      
       
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    DUR (ÀǾàǰ»ç¿ëÆò°¡) 
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	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
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    Mechanism of Action 
    
      Econazole¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Econazole interacts with 14-¥á demethylase, a cytochrome P-450 enzyme necessary to convert lanosterol to ergosterol. As ergosterol is an essential component of the fungal cell membrane, inhibition of its synthesis results in increased cellular permeability causing leakage of cellular contents. Econazole may also inhibit endogenous respiration, interact with membrane phospholipids, inhibit the transformation of yeasts to mycelial forms, inhibit purine uptake, and impair triglyceride and/or phospholipid biosynthesis.Triamcinolone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  The antiinflammatory actions of corticosteroids are thought to involve lipocortins, phospholipase A2 inhibitory proteins which, through inhibition of arachidonic acid, control the biosynthesis of prostaglandins and leukotrienes. The immune system is suppressed by corticosteroids due to a decrease in the function of the lymphatic system, a reduction in immunoglobulin and complement concentrations, the precipitation of lymphocytopenia, and interference with antigen-antibody binding. 
     
   
  
   
    Pharmacology 
     
      Econazole¿¡ ´ëÇÑ Pharmacology Á¤º¸  Econazole is an antifungal medication related to fluconazole (Diflucan), ketoconazole (Nizoral), itraconazole (Sporanox), and clotrimazole (Lotrimin, Mycelex). Econazole prevents fungal organisms from producing vital substances required for growth and function. This medication is effective only for infections caused by fungal organisms. It will not work for bacterial or viral infections.Triamcinolone¿¡ ´ëÇÑ Pharmacology Á¤º¸  Triamcinolone and its derivatives are synthetic glucocorticoids that are used for their antiinflammatory or immunosuppressive properties. 
     
   
  
   
    Metabolism 
    
      Econazole¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Not AvailableTriamcinolone¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Not Available 
     
   
  
   
    Absorption 
    
      Econazole¿¡ ´ëÇÑ Absorption Á¤º¸  After topical application to the skin of normal subjects, systemic absorption of econazole nitrate is extremely low. Although most of the applied drug remains on the skin surface, drug concentrations were found in the stratum corneum which, by far, exceeded the minimum inhibitory concentration for dermatophytes.Triamcinolone¿¡ ´ëÇÑ Absorption Á¤º¸  Rapid absorption following oral administration 
     
   
  
   
    Pharmacokinetics 
    
      Triamcinolone acetonideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
	ÀÛ¿ëÁö¼Ó½Ã°£ : °æ±¸ : 8¡12½Ã°£
	  Èí¼ö : ¿Ü¿ëÁ¦ : Àü½ÅÀûÀ¸·Î Èí¼öµÉ ¼öµµ ÀÖ´Ù.
	  ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : ±ÙÀ°ÁÖ»ç : 8¡10½Ã°£ À̳»
	 »ý¸®Àû ¹Ý°¨±â : 18¡36½Ã°£
  
Econazole NitrateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
Èí¼ö : ¿Ü¿ë : 10% ¹Ì¸¸ 
 ´ë»ç : °£¿¡¼ 20°³ ÀÌ»óÀÇ ´ë»çü·Î ´ë»çµÈ´Ù. 
 ¼Ò½Ç : Åõ¿©·®ÀÇ 1% ¹Ì¸¸ÀÌ ¹Ìº¯Èü·Î ½Å¹è¼³µÇ°Å³ª º¯¹è¼³µÈ´Ù.  
     
   
  
   
    Toxicity 
    
      Econazole¿¡ ´ëÇÑ Toxicity Á¤º¸  Overdosage of econazole in humans has not been reported to date. In mice, rats guinea pigs and dogs, the oral LD 50 values were found to be 462, 668, 272, and > 160 mg/kg, respectively.Triamcinolone¿¡ ´ëÇÑ Toxicity Á¤º¸  LD50 =>500mg/kg (in rats) 
     
   
  
   
    Drug Interactions 
    
      Econazole¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not AvailableTriamcinolone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Econazole¿¡ ´ëÇÑ Food Interaction Á¤º¸  Not AvailableTriamcinolone¿¡ ´ëÇÑ Food Interaction Á¤º¸  Not Available 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Econazole¿¡ ´ëÇÑ Description Á¤º¸  A broad spectrum antimycotic with some action against Gram positive bacteria. It is used topically in dermatomycoses also orally and parenterally. [PubChem]Triamcinolone¿¡ ´ëÇÑ Description Á¤º¸  A glucocorticoid given, as the free alcohol or in esterified form, orally, intramuscularly, by local injection, by inhalation, or applied topically in the management of various disorders in which corticosteroids are indicated. (From Martindale, The Extra Pharmacopoeia, 30th ed, p739) 
     
   
  
   
    Dosage Form 
    
      Econazole¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Suppository	IntravaginalTriamcinolone¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Aerosol, metered	NasalCream	TopicalLiquid	IntramuscularOintment	TopicalPaste	DentalSpray	NasalSuspension	Intra-articularSuspension	IntramuscularSuspension	Intrasynovial 
     
   
  
   
    Drug Category 
    
      Econazole¿¡ ´ëÇÑ Drug_Category Á¤º¸  Antifungal AgentsTriamcinolone¿¡ ´ëÇÑ Drug_Category Á¤º¸  Adrenergic AgentsAnti-inflammatory AgentsGlucocorticoids 
     
   
  
   
    Smiles String Canonical 
    
      Econazole¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  ClC1=CC=C(COC(CN2C=CN=C2)C2=C(Cl)C=C(Cl)C=C2)C=C1Triamcinolone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CC12CC(O)C3(F)C(CCC4=CC(=O)C=CC34C)C1CC(O)C2(O)C(=O)CO 
     
   
  
   
    Smiles String Isomeric 
    
      Econazole¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  ClC1=CC=C(CO[C@@H](CN2C=CN=C2)C2=C(Cl)C=C(Cl)C=C2)C=C1Triamcinolone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  C[C@]12C[C@H](O)[C@@]3(F)[C@@H](CCC4=CC(=O)C=C[C@]34C)[C@@H]1C[C@@H](O)[C@]2(O)C(=O)CO 
     
   
  
   
    InChI Identifier 
    
      Econazole¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C18H15Cl3N2O/c19-14-3-1-13(2-4-14)11-24-18(10-23-8-7-22-12-23)16-6-5-15(20)9-17(16)21/h1-9,12,18H,10-11H2Triamcinolone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C21H27FO6/c1-18-6-5-12(24)7-11(18)3-4-13-14-8-15(25)21(28,17(27)10-23)19(14,2)9-16(26)20(13,18)22/h5-7,13-16,23,25-26,28H,3-4,8-10H2,1-2H3/t13-,14-,15+,16-,18-,19-,20-,21-/m0/s1 
     
   
  
   
    Chemical IUPAC Name 
    
      Econazole¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  1-[2-[(4-chlorophenyl)methoxy]-2-(2,4-dichlorophenyl)ethyl]imidazoleTriamcinolone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  (8S,9R,10S,11S,13S,14S,16R,17S)-9-fluoro-11,16,17-trihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one 
     
   
  
   
    Drug-Induced Toxicity Related Proteins 
    
      TRIAMCINOLONE   ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein  :Serotransferrin Drug  :triamcinolone Toxicity  :stimulate growth of NEL-M1 human melanoma cells . [¹Ù·Î°¡±â] Replated Protein  :InsulinDrug  :triamcinolone Toxicity  :stimulate growth of NEL-M1 human melanoma cells . [¹Ù·Î°¡±â]  
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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                º» ¼öÁ¤ÀÏ Á¤º¸´Â Çã°¡Á¤º¸ ÀÌ¿ÜÀÇ ±âŸÁ¤º¸ ¼öÁ¤ÀÏÀ» ÀǹÌÇϹǷÎ, Çã°¡Á¤º¸¼öÁ¤ÀÏÀº º»¹®¿¡ Ç¥±âµÈ ³¯Â¥¸¦ ÂüÁ¶ÇϽñ⠹ٶø´Ï´Ù.
                 
                   
             
                         
      
           
          
                
                    
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                      µå·°ÀÎÆ÷ ÀǾàÇмúÁ¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×, Çмú¹®Çå, Á¦¾àȸ»ç Á¦°øÁ¤º¸ µîÀ» ±Ù°Å·Î ÀÛ¼ºµÈ Âü°í Á¤º¸ÀÔ´Ï´Ù. 
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                            ¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù. 
                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
 
                    
                  
 
               
  
  
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