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                      131[¾È°ú¿ëÁ¦                                                        ] 
                     
                    
                      
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      Ofloxacin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Ofloxacin acts on DNA gyrase, an enzyme which, like human topoisomerase, prevents the excessive supercoiling of DNA during replication or transcription. 
     
   
  
   
    Pharmacology 
     
      Ofloxacin¿¡ ´ëÇÑ Pharmacology Á¤º¸  Ofloxacin is a quinolone/fluoroquinolone antibiotic. Ofloxacin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase, which allows the untwisting required to replicate one DNA double helix into two. Notably the drug has 100 times higher affinity for bacterial DNA gyrase than for mammalian. Ofloxacin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria. 
     
   
  
   
    Metabolism 
    
      Ofloxacin¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2) 
     
   
  
   
    Protein Binding 
    
      Ofloxacin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  32% 
     
   
  
   
    Half-life 
    
      Ofloxacin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  9 hours 
     
   
  
   
    Absorption 
    
      Ofloxacin¿¡ ´ëÇÑ Absorption Á¤º¸  Bioavailability of ofloxacin in the tablet formulation is approximately 98% 
     
   
  
   
    Pharmacokinetics 
    
      OfloxacinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
Èí¼ö : Àß Èí¼öµÈ´Ù. À½½Ä¹°¿¡ ÀÇÇÑ ¿µÇâÀº ¹Ì¹ÌÇÏ´Ù.
 ºÐÆ÷ : ºÐÆ÷¿ëÀû : 2.4-3.5 L/kg
 ´Ü¹é°áÇÕ : 20%
 ¹Ý°¨±â : 5-7.5 ½Ã°£ 
 ¼Ò½Ç : ÁÖ·Î ¹Ìº¯Èü·Î ½Å¹è¼³
  
     
   
  
   
    Biotransformation 
    
      Ofloxacin¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic 
     
   
  
   
    Toxicity 
    
      Ofloxacin¿¡ ´ëÇÑ Toxicity Á¤º¸  LD50 =5450 mg/kg (orally in mice) 
     
   
  
   
    Drug Interactions 
    
      Ofloxacin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Aluminium	Formation of non-absorbable complexesBismuth	Formation of non-absorbable complexesCalcium	Formation of non-absorbable complexesIron	Formation of non-absorbable complexesMagnesium oxide	Formation of non-absorbable complexesMagnesium	Formation of non-absorbable complexesSucralfate	Formation of non-absorbable complexesZinc	Formation of non-absorbable complexesWarfarin	The quinolone increases the anticoagulant effectAcenocoumarol	The quinolone increases the anticoagulant effectDicumarol	The quinolone increases the anticoagulant effectAnisindione	The quinolone increases the anticoagulant effectDihydroquinidine barbiturate	Increased risk of cardiotoxicity and arrhythmiasQuinidine	Increased risk of cardiotoxicity and arrhythmiasQuinidine barbiturate	Increased risk of cardiotoxicity and arrhythmiasFoscarnet	Increased risk of convulsionsProcainamide	The quinolone increases the effect of procainamide 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Ofloxacin¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take without regard to meals.Avoid high doses of caffeine. 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Ofloxacin¿¡ ´ëÇÑ Description Á¤º¸  A synthetic fluoroquinolone (fluoroquinolones) antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication. [PubChem] 
     
   
  
   
    Drug Category 
    
      Ofloxacin¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti-Bacterial AgentsAnti-Infective Agents, UrinaryAnti-InfectivesNucleic Acid Synthesis InhibitorsQuinolones 
     
   
  
   
    Smiles String Canonical 
    
      Ofloxacin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CC1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N1CCN(C)CC1 
     
   
  
   
    Smiles String Isomeric 
    
      Ofloxacin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  C[C@H]1COC2=C3N1C=C(C(O)=O)C(=O)C3=CC(F)=C2N1CCN(C)CC1 
     
   
  
   
    InChI Identifier 
    
      Ofloxacin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C18H20FN3O4/c1-10-9-26-17-14-11(16(23)12(18(24)25)8-22(10)14)7-13(19)15(17)21-5-3-20(2)4-6-21/h7-8,10H,3-6,9H2,1-2H3,(H,24,25)/f/h24H 
     
   
  
   
    Chemical IUPAC Name 
    
      Ofloxacin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  (+/-)-9-fluoro-2, 3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1, 2, 3-de]-1, 4-benzoxazine-6-carboxylic acid 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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