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	     FDA : Cµî±Þ 
				        
				         (prednicarbate; )
				        
	   
	  
	  
	  
	     
	     
	     
	     
	     
	     
	   
	 
	
	  
	      
	      
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    Mechanism of Action 
    
      Prednicarbate¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  In common with other topical corticosteroids, prednicarbate has anti-inflammatory, antipruritic, and vasoconstrictive properties. In general, the mechanism of the anti-inflammatory activity of topical steroids is unclear. However, corticosteroids are thought to act by the induction of phospholipase A2 inhibitory proteins, collectively called lipocortins. It is postulated that these proteins control the biosynthesis of potent mediators of inflammation such as prostaglandins and leukotrienes by inhibiting the release of their common precursor arachidonic acid. Arachidonic acid is released from membrane phospholipids by phospholipase A2. 
     
   
  
   
    Pharmacology 
     
      Prednicarbate¿¡ ´ëÇÑ Pharmacology Á¤º¸  Corticosteroids diffuse across cell membranes and complex with specific cytoplasmic receptors. These complexes then enter the cell nucleus, bind to DNA (chromatin), and stimulate transcription of messenger RNA (mRNA) and subsequent protein synthesis of various inhibitory enzymes responsible for the anti-inflammatory effects of topical corticosteroids. These anti-inflammatory effects include inhibition of early processes such as edema, fibrin deposition, capillary dilatation, movement of phagocytes into the area, and phagocytic activities. Later processes, such as capillary production, collagen deposition, and keloid formation also are inhibited by corticosteroids. 
     
   
  
   
    Protein Binding 
    
      Prednicarbate¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸  Not Available 
     
   
  
   
    Half-life 
    
      Prednicarbate¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  Not Available 
     
   
  
   
    Absorption 
    
      Prednicarbate¿¡ ´ëÇÑ Absorption Á¤º¸  Absorbed systemically across the stratum corneum. 
     
   
  
   
    Biotransformation 
    
      Prednicarbate¿¡ ´ëÇÑ Biotransformation Á¤º¸  Primarily in skin 
     
   
  
   
    Drug Interactions 
    
      Prednicarbate¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Atazanavir	This gastric pH  modifier decreases the levels/effects of atazanavirDasatinib	Possible decreased levels of dasatinibDigoxin	Rabeprazole increases the effect of digoxinEnoxacin	The agent decreases the absorption of enoxacinIndinavir	Omeprazole decreases the absorption of indinavirItraconazole	The proton pump inhibitor decreases the absorption of imidazoleKetoconazole	The proton pump inhibitor decreases the absorption of imidazole 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Prednicarbate¿¡ ´ëÇÑ Description Á¤º¸  Prednicarbate is a relatively new topical corticosteroid drug. It is similar in potency to hydrocortisone. It is used in the treatment of inflammatory skin diseases, such as atopic dermatitis. It has a favorable benefit-risk ratio, with an inflammatory action similar to that of a medium potency corticosteroid, but with a low potential to cause skin atrophy. The anti-inflammation action of corticosteroids is associated with the inhibition of the interleukin 1-alpha cytokine within keratinocytes. IL-1a is also found in fibroblasts, where it is responsible for proliferation, collagenase induction and IL-6 synthesis, which are related to skin thickness. 
     
   
  
   
    Drug Category 
    
      Prednicarbate¿¡ ´ëÇÑ Drug_Category Á¤º¸  Anti InflammatoryAnti-inflammatory AgentsCorticosteroidGlucocorticoidsSteroidal 
     
   
  
   
    Smiles String Canonical 
    
      Prednicarbate¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CCOC(=O)OC1(CCC2C3CCC4=CC(=O)C=CC4(C)C3C(O)CC12C)C(=O)COC(=O)CC 
     
   
  
   
    Smiles String Isomeric 
    
      Prednicarbate¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CCOC(=O)O[C@]1(CC[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@H]3[C@H](O)C[C@]12C)C(=O)COC(=O)CC 
     
   
  
   
    InChI Identifier 
    
      Prednicarbate¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C27H36O8/c1-5-22(31)34-15-21(30)27(35-24(32)33-6-2)12-10-19-18-8-7-16-13-17(28)9-11-25(16,3)23(18)20(29)14-26(19,27)4/h9,11,13,18-20,23,29H,5-8,10,12,14-15H2,1-4H3 
     
   
  
   
    Chemical IUPAC Name 
    
      Prednicarbate¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  [2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate 
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
 
                    
                  
 
               
  
  
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