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    | Mechanism of Action | 
    
       Dobutamine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Dobutamine directly stimulates beta-1 receptors of the heart to increase myocardial contractility and stroke volume, resulting in increased cardiac output. 
     | 
   
  
   
    | Pharmacology | 
     
       Dobutamine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Dobutamine is a direct-acting inotropic agent whose primary activity results from stimulation of the beta-adrenoceptors of the heart while producing comparatively mild chronotropic, hypertensive, arrhythmogenic, and vasodilative effects. Dobutamine acts primarily on beta-1 adrenergic receptors, with little effect on beta-2 or alpha receptors. It does not cause the release of endogenous norepinephrine, as does dopamine. Dobutamine is indicated when parenteral therapy is necessary for inotropic support in the short-term treatment of patients with cardiac decompensation due to depressed contractility resulting either from organic heart disease or from cardiac surgical procedures. 
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    | Metabolism | 
    
       Dobutamine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Catechol O-methyltransferase (COMT) 
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    | Protein Binding | 
    
       Dobutamine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available 
     | 
   
  
   
    | Half-life | 
    
       Dobutamine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2 minutes 
     | 
   
  
   
    | Absorption | 
    
       Dobutamine¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available 
     | 
   
  
   
    | Biotransformation | 
    
       Dobutamine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available 
     | 
   
  
   
    | Toxicity | 
    
       Dobutamine¿¡ ´ëÇÑ Toxicity Á¤º¸ Not Available 
     | 
   
  
   
    | Drug Interactions | 
    
       Dobutamine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
     | 
   
  
   
    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
     | 
   
  
   
    | Drug Target | 
    
      
      [Drug Target]
     | 
   
  
   
    | Description | 
    
       Dobutamine¿¡ ´ëÇÑ Description Á¤º¸ A beta-2 agonist catecholamine that has cardiac stimulant action without evoking vasoconstriction or tachycardia. It is proposed as a cardiotonic after myocardial infarction or open heart surgery. [PubChem] 
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    | Drug Category | 
    
       Dobutamine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic beta-AgonistsCardiotonic AgentsSympathomimeticSympathomimetics 
     | 
   
  
   
    | Smiles String Canonical | 
    
       Dobutamine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(CCC1=CC=C(O)C=C1)NCCC1=CC(O)=C(O)C=C1 
     | 
   
  
   
    | Smiles String Isomeric | 
    
       Dobutamine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H](CCC1=CC=C(O)C=C1)NCCC1=CC(O)=C(O)C=C1 
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    | InChI Identifier | 
    
       Dobutamine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C18H23NO3/c1-13(2-3-14-4-7-16(20)8-5-14)19-11-10-15-6-9-17(21)18(22)12-15/h4-9,12-13,19-22H,2-3,10-11H2,1H3 
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    | Chemical IUPAC Name | 
    
       Dobutamine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-[2-[4-(4-hydroxyphenyl)butan-2-ylamino]ethyl]benzene-1,2-diol 
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