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                      222[ÁøÇذŴãÁ¦                                                      ] 
                     
                    
                      
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669902800[A60658111]  \0 ¿ø/1g(2010.05.01) (ÇöÀç¾à°¡) \387 ¿ø/1g(2007.08.01) (º¯°æÀü¾à°¡) 
                         
                        
						     
						     
                         
                      
                     
                       
                     
                     
                    
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                      Theophylline  / R03DA04 
                     
                    
                    
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17) St John¡¯s Wort : ÀÌ ¾àÀÇ ´ë»ç°¡ ÃËÁøµÇ¾î Ç÷Áß³óµµ°¡ ÀúÇÏÇÒ À§ÇèÀÌ ÀÖÀ¸¹Ç·Î ÀÌ ¾àÀ» Åõ¿©ÇÏ´Â °æ¿ì St John¡¯s Wort¸¦ ¼·ÃëÇÏÁö ¾Êµµ·Ï ÁÖÀÇÇÑ´Ù.
 
   
  
  
  
   
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    Mechanism of Action 
    
      Theophylline¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Theophylline relaxes the smooth muscle of the bronchial airways and pulmonary blood vessels and reduces airway responsiveness to histamine, methacholine, adenosine, and allergen. Theophylline competitively inhibits type III and type IV phosphodiesterase (PDE), the enzyme responsible for breaking down cyclic AMP in smooth muscle cells, possibly resulting in bronchodilation. Theophylline also binds to the adenosine A2B receptor and blocks adenosine mediated bronchoconstriction. 
     
   
  
   
    Pharmacology 
     
      Theophylline¿¡ ´ëÇÑ Pharmacology Á¤º¸  Theophylline, an xanthine derivative chemically similar to caffeine and theobromine, is used to treat asthma and bronchospasm. Theophylline has two distinct actions in the airways of patients with reversible (asthmatic) obstruction; smooth muscle relaxation (i.e., bronchodilation) and suppression of the response of the airways to stimuli (i.e., non-bronchodilator prophylactic effects). 
     
   
  
   
    Protein Binding 
    
      Theophylline¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  40%, primarily to albumin. 
     
   
  
   
    Half-life 
    
      Theophylline¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  8 hours 
     
   
  
   
    Absorption 
    
      Theophylline¿¡ ´ëÇÑ Absorption Á¤º¸  Theophylline is rapidly and completely absorbed after oral administration in solution or immediate-release solid oral dosage form. 
     
   
  
   
    Pharmacokinetics 
    
      TheophyllineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
	Èí¼ö: °æ±¸ 
	
		 Oxtriphyline(64% theophylline) : Á¦Çü¿¡ µû¶ó 75-100%±îÁö º¯ÇÑ´Ù.
		  Theophylline : Á¦Çü¿¡ µû¶ó 100%±îÁö Èí¼öµÊ
	  
	
	
 ºÐÆ÷ 
	
		 Vd = 0.45L/kg
		  ¸ðÀ¯·Î °ÅÀÇ Ç÷Áß³óµµ¿Í °°Àº Á¤µµ·Î ºÐÆ÷Çϸç Źݵµ Åë°ú
	  
 
 
 
 
 
	  ´ë»ç : °£¿¡¼ demethylation, oxidation
	  ¹Ý°¨±â : ³ªÀÌ, °£ ±â´É, ½É ±â´É, Æó Áúȯ, Èí¿¬·Â¿¡ µû¶ó ¸Å¿ì ´Ù¾ç
	 ¼Ò½Ç : ¼Òº¯
	
		 ¼ºÀÎÀº 10%°¡ ¹Ìº¯Èü·Î ¹è¼³µÇ°í ½Å»ý¾Æ´Â ´õ ¸¹Àº ¾ç(50%±îÁö)ÀÌ ¹Ìº¯Èü·Î ½Å¹è¼³µÈ´Ù.
	  
   
	
     
   
  
   
    Biotransformation 
    
      Theophylline¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic. Biotransformation takes place through demethylation to 1-methylxanthine and 3-methylxanthine and hydroxylation to 1,3-dimethyluric acid. 1-methylxanthine is further hydroxylated, by xanthine oxidase, to 1-methyluric acid. About 6% of a theophylline dose is N-methylated to caffeine. Caffeine and 3-methylxanthine are the only theophylline metabolites with pharmacologic activity. 
     
   
  
   
    Toxicity 
    
      Theophylline¿¡ ´ëÇÑ Toxicity Á¤º¸  Symptoms of overdose include seizures, arrhythmias, and GI effects. 
     
   
  
   
    Drug Interactions 
    
      Theophylline¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] Theophylline¿¡ ´ëÇÑ P450 table SUBSTRATES  
CYP 1A2  
clozapine 
cyclobenzaprine 
imipramine 
mexiletine 
naproxen 
riluzole 
tacrine 
**theophylline**  
INHIBITORS  
CYP 1A2  
cimetidine 
fluoroquinolones 
fluvoxamine 
ticlopidine 
INDUCERS  
CYP 1A2  
tobacco 
 
     
   
  
   
    Description 
    
      Theophylline¿¡ ´ëÇÑ Description Á¤º¸  A methyl xanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervous system stimulant activities.  Theophylline inhibits the 3& 
     
   
  
   
    Drug Category 
    
      Theophylline¿¡ ´ëÇÑ Drug_Category Á¤º¸  Bronchodilator AgentsPhosphodiesterase InhibitorsRespiratory Smooth Muscle RelaxantsVasodilator Agents 
     
   
  
   
    Smiles String Canonical 
    
      Theophylline¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CN1C(=O)N(C)C2=C(NC=N2)C1=O 
     
   
  
   
    Smiles String Isomeric 
    
      Theophylline¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CN1C(=O)N(C)C2=C(NC=N2)C1=O 
     
   
  
   
    InChI Identifier 
    
      Theophylline¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C7H8N4O2/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13/h3H,1-2H3,(H,8,9)/f/h8H 
     
   
  
   
    Chemical IUPAC Name 
    
      Theophylline¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  1,3-dimethyl-7H-purine-2,6-dione 
     
   
  
   
    Drug-Induced Toxicity Related Proteins 
    
      THEOPHYLLINE   ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein  :Renin Drug  :theophylline Toxicity  :low blood pressure . [¹Ù·Î°¡±â] Replated Protein  :Acid sphingomyelinase-like phosphodiesteraseDrug  :Theophylline Toxicity  :emetic side effect. [¹Ù·Î°¡±â] Replated Protein  :Alanine aminotransferaseDrug  :theophylline  Toxicity  :metabolic acidosis. [¹Ù·Î°¡±â]  
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2023-10-04
               
              
                
                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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                            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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