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                    ½ÅÀϸ»·¹ÀλêÆä´Ï¶ó¹ÎÁÖ»ç¾×  PHENIRAMINE SII AMP.[Pheniramine maleate]  
                    
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                     Àü¹®ÀǾàǰ | »èÁ¦ | ºÐ¾÷¿¹¿ÜÀǾàǰ(52)    
                        
                    	
                    
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    141  (Ç×È÷½ºÅ¸¹ÎÁ¦                                                    )
      
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	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
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       [¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
       
       
        
        
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    | Mechanism of Action | 
    
       Pheniramine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Antihistamines such as pheniramine appear to compete with histamine for histamine H1- receptor sites on effector cells. The antihistamines antagonize those pharmacological effects of histamine which are mediated through activation of H1- receptor sites and thereby reduce the intensity of allergic reactions and tissue injury response involving histamine release. 
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    | Pharmacology | 
     
       Pheniramine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pheniramine is an antihistamine used to treat allergic conditions such as hay fever or urticaria. It is generally sold in combination with other medications, rather than as a stand-alone drug. 
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       Pheniramine maleateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
 
- Èí¼ö : °æ±¸ Åõ¿©½Ã ½Å¼ÓÇÏ°Ô Àß Èí¼öµÊ
 
 - ÃÖ°íÇ÷Áß³óµµ µµ´Þ½Ã°£ : °æ±¸ : 1-2.5 ½Ã°£ 
 
 - ºÐÆ÷¿ëÀû : ¾à 150 L
 
 - ¹Ý°¨±â : 16-19 ½Ã°£
 
 - ´ë»ç : °£´ë»ç (chlorpheniramine, brompheniramineº¸´Ù´Â °£´ë»ç¸¦ ¹Þ´Â ºñÀ²ÀÌ ´õ ÀûÀ» °ÍÀ¸·Î ¿©°ÜÁü)
 
 - ¼Ò½Ç : 50-80%°¡ ´¢¸¦ ÅëÇØ (24-43%´Â ¹Ìº¯Èü·Î¼) ¹è¼³µÊ
 
   
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    | Biotransformation | 
    
       Pheniramine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic hydroxylation, demethylation and glucuronidation. 
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    | Toxicity | 
    
       Pheniramine¿¡ ´ëÇÑ Toxicity Á¤º¸ Not Available 
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    | Drug Interactions | 
    
       Pheniramine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Pheniramine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Pheniramine¿¡ ´ëÇÑ Description Á¤º¸ One of the histamine H1 antagonists with little sedative action. It is used in treatment of hay fever, rhinitis, allergic dermatoses, and pruritus. [PubChem] 
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    | Dosage Form | 
    
       Pheniramine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Powder	OralSolution	OralSolution / drops	OralTablet	Oral 
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    | Drug Category | 
    
       Pheniramine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Allergic AgentsAntipruritic AgentsAntipruriticsHistamine H1 Antagonists 
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    | Smiles String Canonical | 
    
       Pheniramine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN(C)CCC(C1=CC=CC=C1)C1=CC=CC=N1 
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    | Smiles String Isomeric | 
    
       Pheniramine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN(C)CC[C@H](C1=CC=CC=C1)C1=CC=CC=N1 
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    | InChI Identifier | 
    
       Pheniramine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C16H20N2/c1-18(2)13-11-15(14-8-4-3-5-9-14)16-10-6-7-12-17-16/h3-10,12,15H,11,13H2,1-2H3 
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    | Chemical IUPAC Name | 
    
       Pheniramine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ N,N-dimethyl-3-phenyl-3-pyridin-2-ylpropan-1-amine 
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    | Drug-Induced Toxicity Related Proteins | 
    
      MALEATE ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Intercellular adhesion molecule 1  Drug:maleate Toxicity:hepatic injury.  [¹Ù·Î°¡±â] 
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