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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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       [Salmeterol] CAS number/89365-50-4 ATC code/R03AC12 PubChem/5152 DrugBank/APRD00277 Formula/C25H37NO4 Mol. mass/415.57 Bioavailability/ ? Metabolism/hepatic CYP3A4 Excretion/ ? Pregnancy cat./
? Legal status/
Prescription Only (S4)(AU) POM(UK) ℞-only(US) Routes/Inhalation Protein binding/96% 
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    | Mechanism of Action | 
    
       Salmeterol¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Salmeterol's long, lipophilic side chain binds to exosites near beta(2)-receptors in the lungs and on bronchiolar smooth muscle, allowing the active portion of the molecule to remain at the receptor site, continually binding and releasing. Beta(2)-receptor stimulation in the lung causes relaxation of bronchial smooth muscle, bronchodilation, and increased bronchial airflow. 
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    | Pharmacology | 
     
       Salmeterol¿¡ ´ëÇÑ Pharmacology Á¤º¸ Salmeterol is a long acting beta2-adrenoceptor agonist (LABA), usually only prescribed for severe persistent asthma following previous treatment with a short-acting beta agonist such as salbutamol and is prescribed concurrently with a corticosteroid, such as beclometasone. The primary noticable difference of salmeterol to salbutamol is that the duration of action lasts approximately 12 hours in comparison with 4-6 hours of salbutamol. When used regularly every day as presecribed, inhaled salmeterol decreases the number and severity of asthma attacks. However, it is not for use for relieving an asthma attack that has already started. Inhaled salmeterol works like other beta 2-agonists, causing bronchodilatation by relaxing the smooth muscle in the airway so as to treat the exacerbation of asthma. Salmeterol is similar in action to formoterol, however formoterol has been demonstrated to have a faster onset of action than salmeterol as a result of a lower lipophilicity, and has also been demonstrated to be more potent - a 12 µg dose of formoterol has been demonstrated to be equivalent to a 50 µg dose of salmeterol. 
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    | Metabolism | 
    
       Salmeterol¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
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    | Protein Binding | 
    
       Salmeterol¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 96% 
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    | Half-life | 
    
       Salmeterol¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 5.5 hours 
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    | Absorption | 
    
       Salmeterol¿¡ ´ëÇÑ Absorption Á¤º¸ Because of the small therapeutic dose, systemic levels of salmeterol are low or undetectable after inhalation of recommended doses. 
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    | Pharmacokinetics | 
    
       SalmeterolÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
	- È¿°ú ¹ßÇö½Ã°£ : 5-20ºÐ (Æò±Õ 10ºÐ)
	
 - ÃÖ°íÈ¿°ú ¹ßÇö½Ã°£ : 2-4½Ã°£
	
 - ÀÛ¿ëÁö¼Ó½Ã°£ : 12 ½Ã°£ 	
	
 - ´Ü¹é°áÇÕ : 94-98%
	
 - ´ë»ç : °£¿¡¼ hydroxylation µÊ
	
 - ¹Ý°¨±â : 3-4 ½Ã°£ 
  
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    | Biotransformation | 
    
       Salmeterol¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic, metabolized by hydroxylation via CYP3A4 
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    | Toxicity | 
    
       Salmeterol¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include angina (chest pain), dizziness, dry mouth, fatigue, flu-like symptoms, headache, heart irregularities, high or low blood pressure, high blood sugar, insomnia, muscle cramps, nausea, nervousness, rapid heartbeat, seizures, and tremor. By the oral route, no deaths occurred in rats at 1,000 mg/kg (approximately 81,000 times the maximum recommended daily inhalation dose in adults and approximately 38,000 times the maximum recommended daily inhalation dose in children on a mg/m2 basis). 
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    | Drug Interactions | 
    
       Salmeterol¿¡ ´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 | 
    
       Salmeterol¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Salmeterol¿¡ ´ëÇÑ Description Á¤º¸ Salmeterol is a long-acting beta2-adrenergic receptor agonist drug that is currently prescribed for the treatment of asthma and chronic obstructive pulmonary disease COPD. 
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    | Drug Category | 
    
       Salmeterol¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic beta-AgonistsBronchodilator AgentsSympathomimetic 
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    | Smiles String Canonical | 
    
       Salmeterol¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ OCC1=C(O)C=CC(=C1)C(O)CNCCCCCCOCCCCC1=CC=CC=C1 
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    | Smiles String Isomeric | 
    
       Salmeterol¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ OCC1=C(O)C=CC(=C1)[C@@H](O)CNCCCCCCOCCCCC1=CC=CC=C1 
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    | InChI Identifier | 
    
       Salmeterol¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C25H37NO4/c27-20-23-18-22(13-14-24(23)28)25(29)19-26-15-7-1-2-8-16-30-17-9-6-12-21-10-4-3-5-11-21/h3-5,10-11,13-14,18,25-29H,1-2,6-9,12,15-17,19-20H2 
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    | Chemical IUPAC Name | 
    
       Salmeterol¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-(hydroxymethyl)-4-[1-hydroxy-2-[6-(4-phenylbutoxy)hexylamino]ethyl]phenol 
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    | Drug-Induced Toxicity Related Proteins | 
    
      SALMETEROL ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Beta-2 adrenergic receptor Drug:Salmeterol  Toxicity:desensitization, cardiovascular effects.  [¹Ù·Î°¡±â] 
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