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                              (2020.03.27) 
                                          
                       
                     
                    
                     
                        
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                      267[¸ð¹ß¿ëÁ¦                                                        ] 
                     
                    
                      
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      ¡¤ ³²¼ºÇü Å»¸ðÁõ(¾Èµå·ÎÁ¨Å»¸ðÁõ) ¹× ¿©¼ºÇü Å»¸ðÁõ(¾Èµå·ÎÁ¨Å»¸ðÁõ)ÀÇ Ä¡·á(2 %, 3 %¿¡ ÇÑÇÔ)
      
     
   
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
  
    
  
  
  
  
  
   
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	     FDA : Cµî±Þ 
				        
				         (minoxidil topical )
				        
	   
	  
	  
	  
	     
	     
	     
	     
	     
	     
	   
	 
	
	  
	      
	      
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      Pharmacokinetics 
      
       
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    DUR (ÀǾàǰ»ç¿ëÆò°¡) 
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	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
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    Mechanism of Action 
    
      Minoxidil¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Minoxidil is thought to promote the survival of human dermal papillary cells (DPCs) or hair cells by activating both extracellular signal-regulated kinase (ERK) and Akt and by preventing cell death by increasing the ratio of BCl- 2/Bax. Minoxidil may stimulate the growth of human hairs by prolonging anagen through these proliferative and anti-apoptotic effects on DPCs. Minoxidil, when used as a vasodilator, acts by opening adenosine triphosphate-sensitive potassium channels in vascular smooth muscle cells. This vasodilation may also improve the viability of hair cells or hair follicles. 
     
   
  
   
    Pharmacology 
     
      Minoxidil¿¡ ´ëÇÑ Pharmacology Á¤º¸  Minoxidil is an orally effective direct acting peripheral vasodilator that reduces elevated systolic and diastolic blood pressure by decreasing peripheral vascular resistance. Minoxidil is also used topically to treat androgenetic alopecia. Microcirculatory blood flow in animals is enhanced or maintained in all systemic vascular beds. In man, forearm and renal vascular resistance decline; forearm blood flow increases while renal blood flow and glomerular filtration rate are preserved. The predominant site of minoxidil action is arterial. Venodilation does not occur with minoxidil; thus, postural hypotension is unusual with its administration. The antihypertensive activity of minoxidil is due to its sulphate metabolite, minoxidil sulfate. 
     
   
  
   
    Absorption 
    
      Minoxidil¿¡ ´ëÇÑ Absorption Á¤º¸  Minoxidil is at least 90% absorbed from the GI tract in experimental animals and man. 
     
   
  
   
    Pharmacokinetics 
    
      MinoxidilÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
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    Toxicity 
    
      Minoxidil¿¡ ´ëÇÑ Toxicity Á¤º¸  Oral LD50  in rats has ranged from 1321-3492 mg/kg; in mice, 2456-2648 mg/kg. Side effects include cardiovascular effects associated with hypotension such as sudden weight gain, rapid heart beat, faintness or dizziness. 
     
   
  
   
    Drug Interactions 
    
      Minoxidil¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Minoxidil¿¡ ´ëÇÑ Description Á¤º¸  A potent direct-acting peripheral vasodilator (vasodilator agents) that reduces peripheral resistance and produces a fall in blood pressure. (From Martindale, The Extra Pharmacopoeia, 30th ed, p371) 
     
   
  
   
    Dosage Form 
    
      Minoxidil¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Liquid	TopicalSolution	TopicalTablet	Oral 
     
   
  
   
    Drug Category 
    
      Minoxidil¿¡ ´ëÇÑ Drug_Category Á¤º¸  Antihypertensive AgentsVasodilator Agents 
     
   
  
   
    Smiles String Canonical 
    
      Minoxidil¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  [H]N=C1N=C(C=C(N)N1O)N1CCCCC1 
     
   
  
   
    Smiles String Isomeric 
    
      Minoxidil¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  [H]\N=C1/N=C(C=C(N)N1O)N1CCCCC1 
     
   
  
   
    InChI Identifier 
    
      Minoxidil¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C9H15N5O/c10-7-6-8(12-9(11)14(7)15)13-4-2-1-3-5-13/h6,11,15H,1-5,10H2/b11-9+ 
     
   
  
   
    Chemical IUPAC Name 
    
      Minoxidil¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  3-hydroxy-2-imino-6-piperidin-1-ylpyrimidin-4-amine 
     
   
    
 
    
     
  
    
       
      
        
          
            
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2025-07-25
               
              
                
                 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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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
 
  
                  
 
               
  
  
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