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    Testosterone ¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸  : Á¤º¸º¸±â  
  Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do  
   
  
   
    Mechanism of Action 
    
      Testosterone¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  The effects of testosterone in humans and other vertebrates occur by way of two main mechanisms: by activation of the androgen receptor (directly or as DHT), and by conversion to estradiol and activation of certain estrogen receptors. Free testosterone (T) is transported into the cytoplasm of target tissue cells, where it can bind to the androgen receptor, or can be reduced to 5¥á-dihydrotestosterone (DHT) by the cytoplasmic enzyme 5¥á-reductase. DHT binds to the same androgen receptor even more strongly than T, so that its androgenic potency is about 2.5 times that of T. The T-receptor or DHT-receptor complex undergoes a structural change that allows it to move into the cell nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects. 
     
   
  
   
    Pharmacology 
     
      Testosterone¿¡ ´ëÇÑ Pharmacology Á¤º¸  Testosterone is a steroid hormone from the androgen group. Testosterone is primarily secreted in the testes of males and the ovaries of females although small amounts are secreted by the adrenal glands. It is the principal male sex hormone and an anabolic steroid. In both males and females, it plays key roles in health and well-being. Examples include enhanced libido, energy, immune function, and protection against osteoporosis. On average, the adult male body produces about twenty times the amount of testosterone than an adult female's body does. 
     
   
  
   
    Metabolism 
    
      Testosterone¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)Cytochrome P450 19 (Aromatase)Monoamine oxidase type A (MAO-A)Cytochrome P450 11A1 (CYP11A1) 
     
   
  
   
    Absorption 
    
      Testosterone¿¡ ´ëÇÑ Absorption Á¤º¸  Approximately 10% of the testosterone dose applied on the skin surface is absorbed into systemic circulation 
     
   
  
   
    Toxicity 
    
      Testosterone¿¡ ´ëÇÑ Toxicity Á¤º¸  Side effects include amnesia, anxiety, discolored hair, dizziness, dry skin, hirsutism, hostility, impaired urination, paresthesia, penis disorder, peripheral edema, sweating, and vasodilation. 
     
   
  
   
    Drug Interactions 
    
      Testosterone¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Not Available 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸]  
     
   
  
   
    Food Interaction 
    
      Testosterone¿¡ ´ëÇÑ Food Interaction Á¤º¸  Not Available 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Testosterone¿¡ ´ëÇÑ Description Á¤º¸  A potent androgenic steroid and major product secreted by the leydig cells of the testis. Its production is stimulated by luteinizing hormone from the pituitary gland. In turn, testosterone exerts feedback control of the pituitary LH and FSH secretion. Depending on the tissues, testosterone can be further converted to dihydrotestosterone or estradiol. [PubChem] 
     
   
  
   
    Dosage Form 
    
      Testosterone¿¡ ´ëÇÑ Dosage_Form Á¤º¸  Capsule	OralGel	TopicalLiquid	IntramuscularPatch	TransdermalSolution	Intramuscular 
     
   
  
   
    Drug Category 
    
      Testosterone¿¡ ´ëÇÑ Drug_Category Á¤º¸  Androgens 
     
   
  
   
    Smiles String Canonical 
    
      Testosterone¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CC12CCC3C(CCC4=CC(=O)CCC34C)C1CCC2O 
     
   
  
   
    Smiles String Isomeric 
    
      Testosterone¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2O 
     
   
  
   
    InChI Identifier 
    
      Testosterone¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3/t14-,15-,16-,17-,18-,19-/m0/s1 
     
   
  
   
    Chemical IUPAC Name 
    
      Testosterone¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  (8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 
     
   
    
 
    
     
  
    
       
      
        
          
            
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2025-10-13
               
              
                
                 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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                      µå·°ÀÎÆ÷ ÀǾàÇмúÁ¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×, Çмú¹®Çå, Á¦¾àȸ»ç Á¦°øÁ¤º¸ µîÀ» ±Ù°Å·Î ÀÛ¼ºµÈ Âü°í Á¤º¸ÀÔ´Ï´Ù. 
                          Á¤º¸ÀÇ Á¤È®¼ºÀ» À§ÇØ ³ë·ÂÇϰí ÀÖÀ¸³ª ÆíÁý»óÀÇ ¿À·ù, Çã°¡»çÇ× º¯°æ, Ãß°¡ÀûÀÎ Çмú¿¬±¸ ¶Ç´Â Àӻ󿬱¸ ¹ßÇ¥ µîÀ¸·Î ÀÎÇØ ¹ß»ýÇÏ´Â ¹®Á¦¿¡ ´ëÇØ µå·°ÀÎÆ÷´Â 
                          Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡± ¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
                            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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