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    | º¸°ü»ó ÁÖÀÇ | 
    
      
    	
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    | Á¶Á¦½Ã ÁÖÀÇ | 
    
      
    	
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    | DUR (ÀǾàǰ»ç¿ëÆò°¡) | 
    º´¿ë±Ý±â :
     
	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
	  [»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]										
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       [¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
       
       
        
        
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    | Mechanism of Action | 
    
       Oxybutynin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Oxybutynin exerts a direct antispasmodic effect on smooth muscle and inhibits the muscarinic action of acetylcholine on smooth muscle. No blocking effects occur at skeletal neuromuscular junctions or autonomic ganglia (antinicotinic effects). 
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    | Pharmacology | 
     
       Oxybutynin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Oxybutynin is an antispasmodic, anticholinergic agent indicated for the treatment of overactive bladder with symptoms of urge urinary incontinence, urgency, and frequency. Oxybutynin relaxes bladder smooth muscle. Oxybutynin exhibits only one-fifth of the anticholinergic activity of atropine on the rabbit detrusor muscle, but four to ten times the antispasmodic activity. Antimuscarinic activity resides predominantly in the R-isomer. 
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    | Metabolism | 
    
       Oxybutynin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4) 
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    | Protein Binding | 
    
       Oxybutynin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 91%-93% 
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    | Half-life | 
    
       Oxybutynin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 12.4-13.2 hours 
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    | Absorption | 
    
       Oxybutynin¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed from gastrointestinal tract. 
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    | Pharmacokinetics | 
    
       Oxybutynin HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
- ÀÛ¿ë¹ßÇö½Ã°£ : 30-60 ºÐ
 
 - ÃÖ´ëÈ¿°ú ¹ßÇö½Ã°£ : 3-6 ½Ã°£
 
 - ÀÛ¿ëÁö¼Ó½Ã°£ : 6-10 ½Ã°£
 
 - Èí¼ö : °æ±¸ : ½Å¼ÓÈ÷ Àß Èí¼öµÊ
 
 - »ýü³»ÀÌ¿ë·ü : °æ±¸ : 6 %
 
 - ´ë»ç : °£´ë»ç
 
	´ë»çü : N-desethyloxybutynin
  
 - ¹Ý°¨±â : 
 
	Parent drug : 1.1-2.3 ½Ã°£ 
 
		controlled-release formulation : ½ÄÈÄ 12½Ã°£, °øº¹½Ã 16 ½Ã°£
  
	N-desethyloxybutynin : ½ÄÈÄ 4½Ã°£, °øº¹½Ã 10½Ã°£ 
  
 - ÃÖ°íÇ÷Áß³óµµ µµ´Þ½Ã°£ : 1 ½Ã°£
 
 - ¼Ò½Ç : ÁÖ·Î ´¢·Î ¹è¼³µÊ
 
  
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    | Biotransformation | 
    
       Oxybutynin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic, primarily by CYP3A4 
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    | Toxicity | 
    
       Oxybutynin¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=1220 mg/kg (Orally in rats, Goldenthal) 
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    | Drug Interactions | 
    
       Oxybutynin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Carbamazepine	Oxybutynin may cause carbamazepine toxicityDonepezil	Possible antagonism of actionGalantamine	Possible antagonism of actionRivastigmine	Possible antagonism of action 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Oxybutynin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take with food. 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Oxybutynin¿¡ ´ëÇÑ Description Á¤º¸ Oxybutynin is an anticholinergic medication used to relieve urinary and bladder difficulties, including frequent urination and inability to control urination, by decreasing muscle spasms of the bladder. It competitively antagonizes the M1, M2, and M3 subtypes of the muscarinic acetylcholine receptor. 
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    | Dosage Form | 
    
       Oxybutynin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Patch	TransdermalSyrup	OralTablet	OralTablet, extended release	Oral 
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    | Drug Category | 
    
       Oxybutynin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anticholinergic AgentsAntispasmodicsGenitourinary Smooth Muscle RelaxantsMuscarinic AntagonistsParasympatholytics 
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    | Smiles String Canonical | 
    
       Oxybutynin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN(CC)CC 
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    | Smiles String Isomeric | 
    
       Oxybutynin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN(CC)CC 
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    | InChI Identifier | 
    
       Oxybutynin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H31NO3/c1-3-23(4-2)17-11-12-18-26-21(24)22(25,19-13-7-5-8-14-19)20-15-9-6-10-16-20/h5,7-8,13-14,20,25H,3-4,6,9-10,15-18H2,1-2H3 
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    | Chemical IUPAC Name | 
    
       Oxybutynin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-diethylaminobut-2-ynyl 2-cyclohexyl-2-hydroxy-2-phenylacetate 
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                ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2023-03-15
              
 
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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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