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    | DUR (ÀǾàǰ»ç¿ëÆò°¡) | 
    º´¿ë±Ý±â :
     
	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
	  [»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]										
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      °í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
      
       [¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
       
       
        
        
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    | Mechanism of Action | 
    
       Clindamycin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Systemic/Vaginal-Clindamycin inhibits protein synthesis of bacteria by binding to the 50 S ribosomal subunits of the bacteria. Topical-Clindamycin reduces free fatty acid concentrations on the skin and to suppress the growth of Propionibacterium acnes (Corynebacterium acnes) , an anaerobe found in sebaceous glands and follicles. 
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    | Pharmacology | 
     
       Clindamycin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Clindamycin is an antibiotic, similar to and a derivative of lincomycin. Clindamycin can be used in topical or systemic treatment. It is effective as an anti-anaerobic antibiotic and antiprotozoal. 
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    | Metabolism | 
    
       Clindamycin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
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    | Protein Binding | 
    
       Clindamycin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 92-94% 
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    | Half-life | 
    
       Clindamycin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2.4 hours 
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    | Absorption | 
    
       Clindamycin¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed after oral administration. Absorption of an oral dose is virtually complete (90%), and the concomitant administration of food does not appreciably modify the serum concentrations; serum levels have been uniform and predictable from person to person and dose to dose. 
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    | Biotransformation | 
    
       Clindamycin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic 
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    | Toxicity | 
    
       Clindamycin¿¡ ´ëÇÑ Toxicity Á¤º¸ Orally and parenterally administered clindamycin has been associated with severe colitis (pseudomembranous colitis) which may result in patient death. Use of the topical formulation of clindamycin results in absorption of the antibiotic from the skin surface. Diarrhea, bloody diarrhea, and colitis (including pseudomembranous colitis) have been reported with the use of topical and systemic clindamycin. 
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    | Drug Interactions | 
    
       Clindamycin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Aluminium	The aluminium salt decreases the absorption of lincosamidesAtracurium	The agent increases the effect of muscle relaxantDihydroxyaluminium	The aluminium salt decreases the absorption of lincosamidesCyclosporine	Decreases the effect of cyclosporineDoxacurium	The agent increases the effect of muscle relaxantGallamine Triethiodide	The agent increases the effect of muscle relaxantMetocurine	The agent increases the effect of muscle relaxantMivacurium	The agent increases the effect of muscle relaxantPancuronium	The agent increases the effect of muscle relaxantPipecuronium	The agent increases the effect of muscle relaxantRocuronium	The agent increases the effect of muscle relaxantSuccinylcholine	The agent increases the effect of muscle relaxantTubocurarine	The agent increases the effect of muscle relaxantVecuronium	The agent increases the effect of muscle relaxantAttapulgite	The aluminium salt decreases the absorption of lincosamidesKaolin	The aluminium salt decreases the absorption of lincosamides 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Clindamycin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food. 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Clindamycin¿¡ ´ëÇÑ Description Á¤º¸ An antibacterial agent that is a semisynthetic analog of lincomycin. [PubChem] 
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    | Dosage Form | 
    
       Clindamycin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule	OralCream	IntravaginalCream	TopicalLiquid	IntramuscularLiquid	IntravenousPowder, for solution	OralSolution	IntravenousSolution	Topical 
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    | Drug Category | 
    
       Clindamycin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsLincomycinsProtein Synthesis Inhibitors 
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    | Smiles String Canonical | 
    
       Clindamycin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCCC1CC(N(C)C1)C(=O)NC(C(C)Cl)C1OC(SC)C(O)C(O)C1O 
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    | Smiles String Isomeric | 
    
       Clindamycin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@H](C)Cl)[C@H]1O[C@H](SC)[C@H](O)[C@@H](O)[C@H]1O 
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    | InChI Identifier | 
    
       Clindamycin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C18H33ClN2O5S/c1-5-6-10-7-11(21(3)8-10)17(25)20-12(9(2)19)16-14(23)13(22)15(24)18(26-16)27-4/h9-16,18,22-24H,5-8H2,1-4H3,(H,20,25)/t9?,10-,11+,12?,13+,14-,15-,16-,18-/m1/s1/f/h20H 
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    | Chemical IUPAC Name | 
    
       Clindamycin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S,4R)-N-[2-chloro-1-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methylsulfanyloxan-2-yl]propyl]-1-methyl-4-propylpyrrolidine-2-carboxamide 
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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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