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    ¸¸¼ºÈ£Èí±âÁúȯ¿¡ Àå±â Åõ¿©µÈ macrolide °è¿ Á¦Á¦¿¡ ´ëÇÏ¿© 
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    ÇöÀç macrolide°è¿(clarithromycin, erythromycin, roxithromycin, azithromycin) Á¦Á¦¸¦ ¸¸¼ºÈ£Èí±â Áúȯ¿¡¼ Àå±â Åõ¿©ÇÏ´Â »ç·Ê°¡ ¹ß»ýÇϰí ÀÖ¾î ÀÌÀÇ ÀÇÇÐÀû Ÿ´ç¼º¿¡ ´ëÇØ ½ÉÀÇÇÔ. 
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   ¡®¸¸¼ºÈ£Èí±âÁúȯ¿¡ Àú¿ë·® Àå±â Åõ¿©(low-dose, long-term therapy)µÈ macrolides°è¿ Á¦Á¦ÀÇ ÀÓ»óÀû À¯¿ë¼º ¹× ¾ÈÀü¼ºÀ» ÀÔÁõÇÒ ¸¸ÇÑ ±Ù°Å´Â ÇöÀç±îÁö ÃæºÐÇÏÁö ¾Ê´Ù°í ÆÇ´ÜµÈ´Ù.¡¯´Â EBH º¸°í¼¸¦ ÂüÁ¶½Ã Â÷ÈÄ macrolides°è Á¦Á¦ÀÇ Àú¿ë·® Àå±â Åõ¿©·Î ÀÎÇÑ ³»¼º±Õ ÃâÇöÀ̳ª ±Õ±³´ëÇö»ó µî ¾ÈÀü¼º ¹× À¯È¿¼º¿¡ ´ëÇÑ ÃæºÐÇÑ ±Ù°Å°¡ È®¸³µÉ ¶§±îÁö ¸¸¼ºÈ£Èí±âÁúȯ¿¡ macrolides°è¿ Á¦Á¦ÀÇ Àú¿ë·® Àå±âÅõ¿©´Â ÇöÇà´ë·Î ½Ä¾àû Çã°¡»çÇ×(¿ë¹ý¿ë·®) µîÀ» ÃʰúÇÑ °æ¿ì·Î º¸¾Æ ÀÎÁ¤ÇÏÁö ¾Æ´ÏÇÔ. 
[2010.06.07 Áø·á½É»çÆò°¡À§¿øÈ¸]  
      
   
  
  
   
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      [Roxithromycin] [Roxithromycin] CAS number  /80214-83-1 ATC code  /J01 FA06 PubChem  /444037 DrugBank  /APRD01305 Formula  /C 41 H 76 N 2 O 15 Mol. mass  /837.047 g/mol Bioavailability  / ? Metabolism  /Liver Excretion  / ? Pregnancy cat.  /
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    Mechanism of Action 
    
      Roxithromycin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Roxithromycin prevents bacteria from growing, by interfering with their protein synthesis. Roxithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Roxithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain gram-negative bacteria, particularly Legionella pneumophila . 
     
   
  
   
    Pharmacology 
     
      Roxithromycin¿¡ ´ëÇÑ Pharmacology Á¤º¸  Roxithromycin is a semi-synthetic macrolide antibiotic. It is very similar in composition, chemical structure and mechanism of action to erythromycin, azithromycin, or clarithromycin. Roxithromycin has the following antibacterial spectrum in vitro : Streptococcus agalactiae , Streptococcus pneumoniae  (Pneumococcus), Neisseria meningitides  (Meningococcus), Listeria monocytogenes , Mycoplasma pneumoniae , Chlamydia trachomatis , Ureaplasma urealyticum , Legionella pneumophila , Helicobacter  (Campylobacter), Gardnerella vaginalis , Bordetella pertussis , Moraxella catarrhalis  (Branhamella Catarrhalis ), and Haemophilus ducreyi . Roxithromycin is highly concentrated in polymorphonuclear leukocytes and macrophages, achieving intracellular concentrations greater than those outside the cell. Roxithromycin enhances the adhesive and chemotactic functions of these cells which in the presence of infection produce phagocytosis and bacterial lysis. Roxithromycin also possesses intracellular bactericidal activity. 
     
   
  
   
    Metabolism 
    
      Roxithromycin¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
     
   
  
   
    Protein Binding 
    
      Roxithromycin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  96%, mainly to alpha1-acid glycoproteins 
     
   
  
   
    Half-life 
    
      Roxithromycin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  12 hours 
     
   
  
   
    Absorption 
    
      Roxithromycin¿¡ ´ëÇÑ Absorption Á¤º¸  Very rapidly absorbed and diffused into most tissues and phagocytes. 
     
   
  
   
    Pharmacokinetics 
    
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		 10% Á¤µµ°¡ ¹Ìº¯Èü·Î ½Å¹è¼³µÈ´Ù. 
	   	  53%°¡ º¯¹è¼³ µÈ´Ù. 
   		  Renal clearance´Â 6 mL/minÀ̰í, nonrenal clearance´Â 43 mL/min ÀÌ´Ù. 
	  
  
     
   
  
   
    Biotransformation 
    
      Roxithromycin¿¡ ´ëÇÑ Biotransformation Á¤º¸  Hepatic. Roxithromycin is only partially metabolised, more than half the parent compound being excreted unchanged. Three metabolites have been identified in urine and faeces: the major metabolite is descladinose roxithromycin, with N-mono and N-di-demethyl roxithromycin as minor metabolites. The respective percentage of roxithromycin and these three metabolites is similar in urine and faeces. 
     
   
  
   
    Toxicity 
    
      Roxithromycin¿¡ ´ëÇÑ Toxicity Á¤º¸  Most common side-effects are gastrointestinal; diarrhoea, nausea, abdominal pain and vomiting. Less common side-effects include headaches, rashes, abnormal liver function values and alteration in senses of smell and taste. 
     
   
  
   
    Drug Interactions 
    
      Roxithromycin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Roxithromycin¿¡ ´ëÇÑ Description Á¤º¸  Roxithromycin is a semi-synthetic macrolide antibiotic. It is very similar in composition, chemical structure and mechanism of action to erythromycin, azithromycin, or clarithromycin. Roxithromycin prevents bacteria from growing, by interfering with their protein synthesis. Roxithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Roxithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain gram-negative bacteria, particularly Legionella pneumophila. It can treat respiratory tract, urinary and soft tissue infections. 
     
   
  
   
    Drug Category 
    
      Roxithromycin¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti-Bacterial Agents 
     
   
  
   
    Smiles String Canonical 
    
      Roxithromycin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=NOCOCCOC)C(C)C(O)C1(C)O 
     
   
  
   
    Smiles String Isomeric 
    
      Roxithromycin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)C[C@@H]([C@H]2O)N(C)C)[C@](C)(O)C[C@@H](C)\C(=N\OCOCCOC)C(C)[C@@H](O)[C@]1(C)O 
     
   
  
   
    InChI Identifier 
    
      Roxithromycin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C41H76N2O15/c1-15-29-41(10,49)34(45)24(4)31(42-53-21-52-17-16-50-13)22(2)19-39(8,48)36(58-38-32(44)28(43(11)12)18-23(3)54-38)25(5)33(26(6)37(47)56-29)57-30-20-40(9,51-14)35(46)27(7)55-30/h22-30,32-36,38,44-46,48-49H,15-21H2,1-14H3/t22-,23-,24+,25+,26-,27+,28+,29-,30+,32-,33+,34-,35+,36-,38+,39-,40-,41-/m1/s1 
     
   
  
   
    Chemical IUPAC Name 
    
      Roxithromycin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R)-6-[(2S,3R,4S,6R)-4-dimethylamino-3-hydroxy-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-(2-methoxyethoxymethoxyimino)-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecan-2-one 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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