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    Acetaminophen ¿¡ ´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 
    
      Acetaminophen¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸  Acetaminophen is thought to act primarily in the CNS, increasing the pain threshold by inhibiting both isoforms of cyclooxygenase, COX-1 and COX-2, enzymes involved in prostaglandin (PG) synthesis. Unlike NSAIDs, acetaminophen does not inhibit cyclooxygenase in peripheral tissues and, thus, has no peripheral anti-inflammatory affects. While aspirin acts as an irreversible inhibitor of COX and directly blocks the enzyme's active site, studies have found that acetaminophen indirectly blocks COX, and that this blockade is ineffective in the presence of peroxides. This might explain why acetaminophen is effective in the central nervous system and in endothelial cells but not in platelets and immune cells which have high levels of peroxides. Studies also report data suggesting that acetaminophen selectively blocks a variant of the COX enzyme that is different from the known variants COX-1 and COX-2. This enzyme is now referred to as COX-3. Its exact mechanism of action is still poorly understood, but future research may provide further insight into how it works. 
     
   
  
   
    Pharmacology 
     
      Acetaminophen¿¡ ´ëÇÑ Pharmacology Á¤º¸  Acetaminophen (USAN) or Paracetamol (INN) is a popular analgesic and antipyretic drug that is used for the relief of fever, headaches, and other minor aches and pains. It is a major ingredient in numerous cold and flu medications and many prescription analgesics. It is extremely safe in standard doses, but because of its wide availability, deliberate or accidental overdoses are not uncommon. Acetaminophen, unlike other common analgesics such as aspirin and ibuprofen, has no anti-inflammatory properties or effects on platelet function, and so it is not a member of the class of drugs known as non-steroidal anti-inflammatory drugs or NSAIDs. In normal doses acetaminophen does not irritate the lining of the stomach nor affect blood coagulation, the kidneys, or the fetal ductus arteriosus (as NSAIDs can). Like NSAIDs and unlike opioid analgesics, acetaminophen does not cause euphoria or alter mood in any way. Acetaminophen and NSAIDs have the benefit of being completely free of problems with addiction, dependence, tolerance and withdrawal. Acetaminophen is used on its own or in combination with pseudoephedrine, dextromethorphan, chlorpheniramine, diphenhydramine, doxylamine, codeine, hydrocodone, or oxycodone. 
     
   
  
   
    Metabolism 
    
      Acetaminophen¿¡ ´ëÇÑ Metabolism Á¤º¸  # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 2E1 (CYP2E1) 
     
   
  
   
    Half-life 
    
      Acetaminophen¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸  1 to 4 hours 
     
   
  
   
    Absorption 
    
      Acetaminophen¿¡ ´ëÇÑ Absorption Á¤º¸  Rapid and almost complete 
     
   
  
   
    Pharmacokinetics 
    
      AcetaminophenÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á  
	´Ü¹é°áÇÕ : 20-50%
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    Biotransformation 
    
      Acetaminophen¿¡ ´ëÇÑ Biotransformation Á¤º¸  Approximately 90 to 95% of a dose is metabolized in the liver via the cytochrome P450 enzyme pathways (primarily by conjugation with glucuronic acid, sulfuric acid, and cysteine). An intermediate metabolite is hepatotoxic and most likely nephrotoxic and can accumulate after the primary metabolic pathways have been saturated. 
     
   
  
   
    Toxicity 
    
      Acetaminophen¿¡ ´ëÇÑ Toxicity Á¤º¸  Oral, mouse: LD50  = 338 mg/kg; Oral, rat: LD50  = 1944 mg/kg. Acetaminophen is metabolized primarily in the liver, where most of it is converted to inactive compounds by conjugation with sulfate and glucuronide, and then excreted by the kidneys. Only a small portion is metabolized via the hepatic cytochrome P450 enzyme system. The toxic effects of acetaminophen are due to a minor alkylating metabolite (N-acetyl-p-benzo-quinone imine), not acetaminophen itself nor any of the major metabolites. This toxic metabolite reacts with sulfhydryl groups. At usual doses, it is quickly detoxified by combining irreversibly with the sulfhydryl group of glutathione to produce a non-toxic conjugate that is eventually excreted by the kidneys. The toxic dose of paracetamol is highly variable. In adults, single doses above 10 grams or 140 mg/kg have a reasonable likelihood of causing toxicity. In adults, single doses of more than 25 grams have a high risk of lethality. 
     
   
  
   
    Drug Interactions 
    
      Acetaminophen¿¡ ´ëÇÑ Drug_Interactions Á¤º¸  Anisindione	Acetaminophen  increases the anticoagulant effectWarfarin	Acetaminophen increases the anticoagulant effectImatinib	Increased hepatic toxicity of both agentsIsoniazid	Risk of hepatotoxicityDicumarol	Acetaminophen increases the anticoagulant effectDicumarol	Increases the anticoagulant effectAcenocoumarol	Increases the anticoagulant effect 
     
   
  
   
    CYP450  Drug Interaction 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] Acetaminophen¿¡ ´ëÇÑ P450 table SUBSTRATES  
CYP 2E1  
**acetaminophen**  
chlorzoxazone 
ethanol 
INHIBITORS  
CYP 2E1  
disulfiram 
INDUCERS  
CYP 2E1  
ethanol 
isoniazid 
 
     
   
  
   
    Food Interaction 
    
      Acetaminophen¿¡ ´ëÇÑ Food Interaction Á¤º¸  Take without regard to meals.Avoid alcohol (may increase risk of hepatotoxicity). 
     
   
  
   
    Drug Target 
    
      
      [Drug Target]  
     
   
  
   
    Description 
    
      Acetaminophen¿¡ ´ëÇÑ Description Á¤º¸  Analgesic antipyretic derivative of acetanilide. It has weak anti-inflammatory properties and is used as a common analgesic, but may cause liver, blood cell, and kidney damage. [PubChem] 
     
   
  
   
    Drug Category 
    
      Acetaminophen¿¡ ´ëÇÑ Drug_Category Á¤º¸  Analgesics, Non-NarcoticAntipyretics 
     
   
  
   
    Smiles String Canonical 
    
      Acetaminophen¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸  CC(=O)NC1=CC=C(O)C=C1 
     
   
  
   
    Smiles String Isomeric 
    
      Acetaminophen¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸  CC(=O)NC1=CC=C(O)C=C1 
     
   
  
   
    InChI Identifier 
    
      Acetaminophen¿¡ ´ëÇÑ InChI_Identifier Á¤º¸  InChI=1/C8H9NO2/c1-6(10)9-7-2-4-8(11)5-3-7/h2-5,11H,1H3,(H,9,10)/f/h9H 
     
   
  
   
    Chemical IUPAC Name 
    
      Acetaminophen¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸  N-(4-hydroxyphenyl)acetamide 
     
   
  
   
    Drug-Induced Toxicity Related Proteins 
    
      ACETAMINOPHEN   ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein  :Alpha-2A adrenergic receptor Drug  :acetaminophen Toxicity  :hepatic injury . [¹Ù·Î°¡±â] Replated Protein  :Myeloperoxidase Drug  :acetaminophen Toxicity  :respiratory burst. [¹Ù·Î°¡±â] Replated Protein  :Glucose-6-phosphate 1-dehydrogenaseDrug  :acetaminophen Toxicity  :drug-induced hemolysis. [¹Ù·Î°¡±â] Replated Protein  :Ornithine decarboxylaseDrug  :acetaminophen Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Lactate dehydrogenaseDrug  :acetaminophen Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Transcription factor AP-1(JUN)Drug  :acetaminophen Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Haptoglobin Drug  :acetaminophen Toxicity  :drug-induced hemolysis. [¹Ù·Î°¡±â] Replated Protein  :Alanine aminotransferaseDrug  :acetaminophen Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Beta-glucuronidase Drug  :acetaminophen Toxicity  :hepatotoxin-induced effects. [¹Ù·Î°¡±â] Replated Protein  :CYP2E1Drug  :Acetaminophen Toxicity  :idiosyncratic hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Cytochrome P450 2E1 Drug  :acetaminophen  Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Sulfotransferase family cytosolicDrug  :acetaminophen  Toxicity  :chronic hypoxia. [¹Ù·Î°¡±â] Replated Protein  :Cytochrome P450 3A4 Drug  :acetaminophen  Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Caspase recruitment domain-containing protein Drug  :acetaminophen  Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] Replated Protein  :Cytochrome P450 1A2 Drug  :acetaminophen  Toxicity  :hepatotoxicity. [¹Ù·Î°¡±â] ACETAMINOPHEN (APAP)   ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸Replated Protein  :Cytochrome P450Drug  :acetaminophen (APAP) Toxicity  :renal functional changes, strain-dependent histopathological changes. [¹Ù·Î°¡±â]  
     
   
    
 
	  
	   
	
	  
       
	    
	      
	        
            
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2025-04-08
               
              
                
                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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