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	    º¹¾àÀ̹ÌÁöÀÇ Ç¥½Ã¿©ºÎ´Â ½ÇÁ¦ ¾à¹°º¹¿ë½Ã Á߿䵵¿¡ µû¸¥°ÍÀº ¾Æ´Ï¸ç ´Ü¼øÈ÷ Çã°¡Á¤º¸»ó Ű¿öµå¸¦ ±âÁØÀ¸·Î µî·ÏµÇ¾ú½À´Ï´Ù. | 
	   
	  
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	    ±ÍÇϰ¡ º¹¾àÀ̹ÌÁö Á¤º¸¸¦ ½Å·ÚÇÔÀº ÀüÀûÀ¸·Î ±ÍÇÏÀÇ Ã¥ÀÓÀÔ´Ï´Ù. µå·°ÀÎÆ÷´Â ÀÌ¿¡ ´ëÇÑ ¾î¶°ÇÑ º¸Áõµµ ÇÏÁö ¾Ê½À´Ï´Ù. | 
	   
	   
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    | º¸°ü»ó ÁÖÀÇ | 
    
      
    	
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	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
	  [»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]										
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       [¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
       
       
        
        
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    | Mechanism of Action | 
    
       Ceftibuten¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Ceftibuten exerts its bactericidal action by binding to essential target proteins of the bacterial cell wall. This binding leads to inhibition of cell-wall synthesis. 
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    | Pharmacology | 
     
       Ceftibuten¿¡ ´ëÇÑ Pharmacology Á¤º¸ Ceftibuten is a third-generation cephalosporin antibiotic. 
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    | Protein Binding | 
    
       Ceftibuten¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Ceftibuten is 65% bound to plasma proteins. The protein binding is independent of plasma ceftibuten concentration. 
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    | Half-life | 
    
       Ceftibuten¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available 
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    | Absorption | 
    
       Ceftibuten¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed following oral administration. 
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    | Pharmacokinetics | 
    
       CeftibutenÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
- Èí¼ö : °æ±¸ : 
	
	-   ½Å¼ÓÇÏ°Ô Èí¼öµÈ´Ù.  
	
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 - ¹Ý°¨±â : 2½Ã°£
 - Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 2-3 ½Ã°£
 - ¼Ò½Ç : ½Å¹è¼³
  
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    | Biotransformation | 
    
       Ceftibuten¿¡ ´ëÇÑ Biotransformation Á¤º¸ A study with radiolabeled ceftibuten administered to 6 healthy adult male volunteers demonstrated that cis-ceftibuten is the predominant component in both plasma and urine. About 10% of ceftibuten is converted to the trans-isomer is approximately 1/8 as antimicrobially potent as the cis-isomer. 
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    | Toxicity | 
    
       Ceftibuten¿¡ ´ëÇÑ Toxicity Á¤º¸ Overdosage of cephalosporins can cause cerebral irritation leading to convulsions. 
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    | Drug Interactions | 
    
       Ceftibuten¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Ceftibuten¿¡ ´ëÇÑ Description Á¤º¸ Ceftibuten is a third-generation cephalosporin antibiotic. It is an orally-administered agent. Cefalexin is used to treat acute bacterial exacerbations of chronic bronchitis (ABECB), acute bacterial otitis media, pharyngitis, and tonsilitis. 
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    | Dosage Form | 
    
       Ceftibuten¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule	OralSuspension	Oral 
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    | Drug Category | 
    
       Ceftibuten¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsCephalosporins 
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    | Smiles String Canonical | 
    
       Ceftibuten¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ O.O.NC1=NC(=CS1)C(=CCC(O)=O)C(=O)NC1C2SCC=C(N2C1=O)C(O)=O 
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    | Smiles String Isomeric | 
    
       Ceftibuten¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ O.O.NC1=NC(=CS1)\C(=C\CC(O)=O)C(=O)N[C@H]1[C@H]2SCC=C(N2C1=O)C(O)=O 
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    | InChI Identifier | 
    
       Ceftibuten¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H14N4O6S2.2H2O/c16-15-17-7(5-27-15)6(1-2-9(20)21)11(22)18-10-12(23)19-8(14(24)25)3-4-26-13(10)19;;/h1,3,5,10,13H,2,4H2,(H2,16,17)(H,18,22)(H,20,21)(H,24,25);2*1H2/b6-1-;;/t10-,13-;;/m1../s1/f/h18,20,24H,16H2;; 
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    | Chemical IUPAC Name | 
    
       Ceftibuten¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (6R,7R)-7-[[(Z)-2-(2-amino-1,3-thiazol-4-yl)-5-hydroxy-5-oxopent-2-enoyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid dihydrate 
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2013-09-02
              
 
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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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                            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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