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    Ketoprofen ¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸  : Á¤º¸º¸±â  
  Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do  
   
  
   
    Mechanism of Action 
    
      Ketoprofen¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Ketoprofen is a nonsteroidal anti-inflammatory drug with analgesic and antipyretic properties. Its antiinflammatory effects are believed to be due to inhibition of both cylooxygenase-1 (COX-1) and cylooxygenase-2 (COX-2) which leads to the inhibition of prostaglandin synthesis, and leukotriene synthesis, to have antibrady-kinin activity, as well as to have lysosomal membrane-stabilizing action. Antipyretic effects may be due to action on the hypothalamus, resulting in an increased peripheral blood flow, vasodilation, and subsequent heat dissipation. 
     
   
  
   
    Pharmacology 
     
      Ketoprofen¿¡ ´ëÇÑ Pharmacology Á¤º¸  Ketoprofen is a nonsteroidal antiinflammatory drug (NSAID) with analgesic and antipyretic properties. Ketoprofen has pharmacologic actions similar to those of other prototypical NSAIDs, that is thought to be associated with the inhibition of prostaglandin synthesis. Ketoprofen is used to treat rheumatoid arthritis, osteoarthritis, dysmenorrhea, and to alleviate moderate pain. 
     
   
  
   
    Metabolism 
    
      Ketoprofen¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Not Available 
     
   
  
   
    Protein Binding 
    
      Ketoprofen¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  99% 
     
   
  
   
    Half-life 
    
      Ketoprofen¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  2-2.5 hours 
     
   
  
   
    Absorption 
    
      Ketoprofen¿¡ ´ëÇÑ Absorption Á¤º¸  Ketoprofen is rapidly and well-absorbed orally, with peak plasma levels occurring within 0.5 to 2 hours. 
     
   
  
   
    Biotransformation 
    
      Ketoprofen¿¡ ´ëÇÑ Biotransformation Á¤º¸  Not Available 
     
   
  
   
    Toxicity 
    
      Ketoprofen¿¡ ´ëÇÑ Toxicity Á¤º¸  LD50 =62.4 mg/kg (rat, oral) Adverse effects from overdose include breathing difficulty, coma, convulsions, drowsiness, high blood pressure, kidney failure, low blood pressure, nausea, sluggishness, stomach and intestinal bleeding, stomach pain, vomiting. 
     
   
  
   
    Drug Interactions 
    
      Ketoprofen¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Alendronate	Increased risk of gastric toxicityMethotrexate	The NSAID increases the effect and toxicity of methotrexateCyclosporine	Monitor for nephrotoxicityAnisindione	The NSAID increases the anticoagulant effectAcenocoumarol	The NSAID increases the anticoagulant effectDicumarol	The NSAID increases the anticoagulant effectWarfarin	The NSAID increases the anticoagulant effect 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Ketoprofen¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take with food to reduce irritation, avoid alcohol. 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Ketoprofen¿¡ ´ëÇÑ Description Á¤º¸  An ibuprofen-type anti-inflammatory analgesic and antipyretic. It is used in the treatment of rheumatoid arthritis and osteoarthritis. [PubChem] 
     
   
  
   
    Dosage Form 
    
      Ketoprofen¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Capsule	OralSuppository	RectalTablet, coated	OralTablet, extended release	Oral 
     
   
  
   
    Drug Category 
    
      Ketoprofen¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti-Inflammatory Agents, Non-SteroidalCyclooxygenase Inhibitors 
     
   
  
   
    Smiles String Canonical 
    
      Ketoprofen¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CC(C(O)=O)C1=CC(=CC=C1)C(=O)C1=CC=CC=C1 
     
   
  
   
    Smiles String Isomeric 
    
      Ketoprofen¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  C[C@@H](C(O)=O)C1=CC(=CC=C1)C(=O)C1=CC=CC=C1 
     
   
  
   
    InChI Identifier 
    
      Ketoprofen¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)/f/h18H 
     
   
  
   
    Chemical IUPAC Name 
    
      Ketoprofen¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  2-[3-(benzoyl)phenyl]propanoic acid 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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