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ÀӽŠÁ¦ 3 »ïºÐ±â µ¿¾È Ç÷縣ºñÇÁ·ÎÆæÀ» Æ÷ÇÔÇÑ ÇÁ·Î½ºÅ¸±Û¶õµò ÇÕ¼ºÈ¿¼Ò ¾ïÁ¦Á¦¸¦ Àü½ÅÀûÀ¸·Î »ç¿ëÇϸé žƿ¡°Ô ½ÉÆó ¹× ½ÅÀå µ¶¼ºÀ» À¯¹ßÇÒ ¼ö ÀÖÀ¸¸ç, ÀӽЏ»±â¿¡´Â »ê¸ð¿Í ¾ÆÀÌ ¸ðµÎ ÃâÇ÷ ½Ã°£ÀÌ ±æ¾îÁö°í ÁøÅëÀÌ Áö¿¬µÉ ¼ö ÀÖ´Ù. µû¶ó¼ Ç÷縣ºñÇÁ·ÎÆæÀº ÀӽŠÈı⿡´Â Åõ¿©ÇÏÁö ¸¶½Ê½Ã¿À.
     
   
  
  
  
  
  
  
  
   
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    Àû¿ë»óÀÇ ÁÖÀÇ 
    1) ¼Õ»óµÈ ÇÇºÎ¿Í Á¡¸·¿¡´Â »ç¿ëÇÏÁö ¸¶½Ê½Ã¿À.
2) ½ÀÁø ¶Ç´Â ¹ßÁøºÎÀ§¿¡´Â »ç¿ëÇÏÁö ¸¶½Ê½Ã¿À.
3) Àû¿ëºÎÀ§ÀÇ ¶¡À» ´Û¾Æ³½ ÈÄ »ç¿ëÇϽʽÿÀ.
 
   
  
  
  
  
  
  		
  
  
   
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				         (flurbiprofen; )
				        
	   
	  
	  
	  
	     
	     
	     
	     
	     
	     
	   
	 
	
	  
	      
	      
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      Pharmacokinetics 
      
       
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    Mechanism of Action 
    
      Flurbiprofen¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  The antiinflammatory effect of flurbiprofen may result from the reversible inhibition of cyclooxygenase, causing the peripheral inhibition of prostaglandin synthesis. Flurbiprofen also inhibits the migration of leukocytes into sites of inflammation and prevents the formation of thromboxane A2, an aggregating agent, by the platelets. 
     
   
  
   
    Pharmacology 
     
      Flurbiprofen¿¡ ´ëÇÑ Pharmacology Á¤º¸  Flurbiprofen, a nonsteroidal antiinflammatory drug (NSAID) of the propionic acid class, is used for the relief of pain and inflammation associated with rheumatoid arthritis and osteoarthritis and for the inhibition of intraoperative miosis. Flurbiprofen exhibits antiinflammatory, analgesic, and antipyretic activities. 
     
   
  
   
    Metabolism 
    
      Flurbiprofen¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2C9 (CYP2C9) 
     
   
  
   
    Protein Binding 
    
      Flurbiprofen¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  > 99% 
     
   
  
   
    Half-life 
    
      Flurbiprofen¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  4.7-5.7 hours 
     
   
  
   
    Absorption 
    
      Flurbiprofen¿¡ ´ëÇÑ Absorption Á¤º¸  The mean oral bioavailability of flurbiprofen from tablets is 96% relative to an oral solution. 
     
   
  
   
    Pharmacokinetics 
    
      FlurbiprofenÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
	ÀÛ¿ë¹ßÇö½Ã°£ : 1-2 ½Ã°£ À̳»
  
     
   
  
   
    Biotransformation 
    
      Flurbiprofen¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic. Cytochrome P450 2C9 plays an important role in the metabolism of flurbiprofen to its major metabolite, 4¡¯-hydroxy-flurbiprofen. The 4¡¯-hydroxy-flurbiprofen metabolite showed little anti-inflammatory activity in animal models of inflammation. 
     
   
  
   
    Toxicity 
    
      Flurbiprofen¿¡ ´ëÇÑ Toxicity Á¤º¸  LD50 =10 mg/kg (orally in dogs). 
     
   
  
   
    Drug Interactions 
    
      Flurbiprofen¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Alendronate	Increased risk of gastric toxicityMethotrexate	The NSAID increases the effect and toxicity of methotrexateAnisindione	The NSAID increases the anticoagulant effectDicumarol	The NSAID increases the anticoagulant effectAcenocoumarol	The NSAID increases the anticoagulant effectWarfarin	The NSAID increases the anticoagulant effectCyclosporine	Monitor for nephrotoxicity 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Flurbiprofen¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take with food to reduce irritation.Avoid alcohol. 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Flurbiprofen¿¡ ´ëÇÑ Description Á¤º¸  An anti-inflammatory analgesic and antipyretic of the phenylalkynoic acid series. It has been shown to reduce bone resorption in periodontal disease by inhibiting carbonic anhydrase. [PubChem] 
     
   
  
   
    Dosage Form 
    
      Flurbiprofen¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Capsule, extended release	OralLiquid	OphthalmicTablet	Oral 
     
   
  
   
    Drug Category 
    
      Flurbiprofen¿¡ ´ëÇÑ Drug_Category Á¤º¸  AnalgesicsAnti-Inflammatory Agents, Non-SteroidalAnti-inflammatory AgentsCarbonic Anhydrase InhibitorsCyclooxygenase InhibitorsNonsteroidal Antiinflammatory Agents (NSAIDs) 
     
   
  
   
    Smiles String Canonical 
    
      Flurbiprofen¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CC(C(O)=O)C1=CC(F)=C(C=C1)C1=CC=CC=C1 
     
   
  
   
    Smiles String Isomeric 
    
      Flurbiprofen¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  C[C@@H](C(O)=O)C1=CC(F)=C(C=C1)C1=CC=CC=C1 
     
   
  
   
    InChI Identifier 
    
      Flurbiprofen¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)/f/h17H 
     
   
  
   
    Chemical IUPAC Name 
    
      Flurbiprofen¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  2-(3-fluoro-4-phenylphenyl)propanoic acid 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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