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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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      °í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
      
       [¿¬·É´ë±Ý±â»ó¼¼°Ë»ö]
       
       
        
        
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    | µ¶¼ºÁ¤º¸ | 
    Digoxin¿¡ ´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 | 
    
       Digoxin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Digoxin inhibits the Na-K-ATPase membrane pump, resulting in an increase in intracellular sodium and calcium concentrations. Increased intracellular concentrations of calcium may promote activation of contractile proteins (e.g., actin, myosin). Digoxin also acts on the electrical activity of the heart, increasing the slope of phase 4 depolarization, shortening the action potential duration, and decreasing the maximal diastolic potential. 
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    | Pharmacology | 
     
       Digoxin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Digoxin, a cardiac glycoside similar to digitoxin, is used to treat congestive heart failure and supraventricular arrhythmias due to reentry mechanisms, and to control ventricular rate in the treatment of chronic atrial fibrillation. 
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    | Metabolism | 
    
       Digoxin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 11A1 (CYP11A1) 
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    | Protein Binding | 
    
       Digoxin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 25% 
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    | Half-life | 
    
       Digoxin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 3.5 to 5 days 
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    | Absorption | 
    
       Digoxin¿¡ ´ëÇÑ Absorption Á¤º¸ Absorption of digoxin from the elixir pediatric formulation has been demonstrated to be 70% to 85% complete (90% to 100% from the capsules, and 60% to 80% for tablets). 
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    | Biotransformation | 
    
       Digoxin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic (but not dependent upon the cytochrome P-450 system). The end metabolites, which include 3 b-digoxigenin, 3-keto-digoxigenin, and their glucuronide and sulfate conjugates, are polar in nature and are postulated to be formed via hydrolysis, oxidation, and conjugation. 
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    | Toxicity | 
    
       Digoxin¿¡ ´ëÇÑ Toxicity Á¤º¸ Toxicity includes ventricular tachycardia or ventricular fibrillation, or progressive bradyarrhythmias, or heart block. LD50 = 7.8 mg/kg (orally in mice). 
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    | Drug Interactions | 
    
       Digoxin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Acarbose	Acarbose decreases the effect of digoxinAlprazolam	The benzodiazepine increases the effect of digoxinAmiodarone	Amiodarone increases the effect of digoxinBendroflumethiazide	Possible electrolyte variations and arrhythmiasBenzthiazide	Possible electrolyte variations and arrhythmiasBleomycin	The antineoplasic agent decreases the effect of digoxinBumetanide	Possible electrolyte variations and arrhythmiasCarmustine	The antineoplasic agent decreases the effect of digoxinCarvedilol	Carvedilol increases levels/effect of digoxinChlorothiazide	Possible electrolyte variations and arrhythmiasChlorthalidone	Possible electrolyte variations and arrhythmiasCholestyramine	The resin decreases the effect of digoxinClarithromycin	The macrolide increases the effect of digoxin in 10% of patientsColestipol	The resin decreases the effect of digoxinCyclophosphamide	The antineoplasic agent decreases the effect of digoxinCyclosporine	Cyclosporine increases the effect of digoxinCyclothiazide	Possible electrolyte variations and arrhythmiasCytarabine	The antineoplasic agent decreases the effect of digoxinDemeclocycline	The tetracycline increases the effect of digoxin in 10% of patientsDextrothyroxine	The thyroid hormone decreases the effect of digoxinDiazepam	The benzodiazepine increases the effect of digoxinDihydroquinidine barbiturate	Quinine/quinidine increases the effect of digoxinDoxorubicin	The antineoplasic agent decreases the effect of digoxinDoxycycline	The tetracycline increases the effect of digoxin in 10% of patientsErythromycin	The macrolide increases the effect of digoxin in 10% of patientsEthacrynic acid	Possible electrolyte variations and arrhythmiasFurosemide	Possible electrolyte variations and arrhythmiasGatifloxacin	Gatifloxacin increases the effect of digoxinGinseng	Changes in digoxin serum levelsHydrochlorothiazide	Possible electrolyte variations and arrhythmiasHydroflumethiazide	Possible electrolyte variations and arrhythmiasItraconazole	Itraconazole increases the effect of digoxinIndapamide	Possible electrolyte variations and arrhythmiasJosamycin	The macrolide increases the efect of digoxin in 10% of patientsLevothyroxine	The thyroid hormones decreases the effect of digoxinLiothyronine	The thyroid hormones decreases the effect of digoxinMethacycline	The tetracycline increases the effect of digoxin in 10% of patientsMethimazole	The antithyroid agent increases the effect of digoxinMethyclothiazide	Possible electrolyte variations and arrhythmiasMetolazone	Possible electrolyte variations and arrhythmiasMinocycline	The tetracycline increases the effect of digoxin in 10% of patientsOxytetracycline	The tetracycline increases the effect of digoxin in 10% of patientsPenicillamine	Penicillamine decreases the effect of digoxinPolythiazide	Possible electrolyte variations and arrhythmiasPrazosin	Prazosin increases the effect of digoxinProcarbazine	The antineoplasic agent decreases the effect of digoxinPropafenone	Propafenone increases the effect of digoxinPropylthiouracil	The antithyroid agent increases the effect of digoxinQuinethazone	Possible electrolyte variations and arrhythmiasQuinidine	Quinine/quinidine increases the effect of digoxinQuinidine barbiturate	Quinine/quinidine increases the effect of digoxinRabeprazole	Rabeprazole increases the effect of digoxinRanolazine	Ranolazine increases digoxin's levelsRitonavir	Ritonavir increases levels/effect of digoxinRolitetracycline	The tetracycline increases the effect of digoxin in 10% of patientsSpironolactone	Increased digoxin levels and decreased effect in presence of spironolactoneSt. John's Wort	St. John's Wort decreases the effect of digoxinSulfasalazine	Sulfasalazine decreases the effect of digoxinTelithromycin	Telithromycin may increase levels of digoxinTelmisartan	Telmisartan increases the effect of digoxinTetracycline	The tetracycline increases the effect of digoxin in 10% of patientsTolbutamide	Tolbutamide increases the effect of digoxinTrichlormethiazide	Possible electrolyte variations and arrhythmiasVerapamil	Verapamil increases the effect of digoxinVincristine	The antineoplasic agent decreases the effect of digoxinMethotrexate	The antineoplasic agent decreases the effect of digoxinHydroxychloroquine	Hydroxychloroquine increases the effect of digoxinLiotrix	The thyroid hormone decreases the effect of digoxinThyroglobulin	The thyroid hormone decreases the effect of digoxinQuinine	Quinine/quinidine increases the effect of digoxin 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Digoxin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid bran and high fiber foods within 2 hours of taking this medication.Avoid excess salt/sodium unless otherwise instructed by your physician.Avoid salt substitutes containing potassium.Avoid milk, calcium containing dairy products, iron, antacids, or aluminum salts 2 hours before or 6 hours after using antacids while on this medication.Limit garlic, ginger, gingko, and horse chestnut.Avoid avocado. 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       Digoxin¿¡ ´ëÇÑ Description Á¤º¸ A cardiotonic glycoside obtained mainly from Digitalis lanata; it consists of three sugars and the aglycone digoxigenin. Digoxin has positive inotropic and negative chronotropic activity. It is used to control ventricular rate in atrial fibrillation and in the management of congestive heart failure with atrial fibrillation. Its use in congestive heart failure and sinus rhythm is less certain. The margin between toxic and therapeutic doses is small. (From Martindale, The Extra Pharmacopoeia, 30th ed, p666) 
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    | Dosage Form | 
    
       Digoxin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Liquid	IntravenousPowder, for solution	IntravenousSolution	OralTablet	Oral 
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    | Drug Category | 
    
       Digoxin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Arrhythmia AgentsAntiarrhythmic AgentsCardiotonic AgentsEnzyme Inhibitors 
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    | Smiles String Canonical | 
    
       Digoxin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1OC(CC(O)C1O)OC1C(O)CC(OC1C)OC1C(O)CC(OC2CCC3(C)C(CCC4C3CC(O)C3(C)C(CCC43O)C3=CC(=O)OC3)C2)OC1C 
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    | Smiles String Isomeric | 
    
       Digoxin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H]1O[C@H](C[C@H](O)[C@@H]1O)O[C@H]1[C@@H](O)C[C@@H](O[C@@H]1C)O[C@H]1[C@@H](O)C[C@H](O[C@H]2CC[C@@]3(C)[C@H](CC[C@@H]4[C@@H]3C[C@@H](O)[C@]3(C)[C@H](CC[C@]43O)C3=CC(=O)OC3)C2)O[C@@H]1C 
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    | InChI Identifier | 
    
       Digoxin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25?,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1 
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    | Chemical IUPAC Name | 
    
       Digoxin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-[(3S,5R,8R,9S,10S,12R,13S,14S)-3-[(2R,4S,5S,6R)-5-[(2S,4S,5S,6R)-5-[(2S,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-6-methyloxan-2-yl]oxy-4-hydroxy-6-methyloxan-2-yl]oxy-12,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-5H-furan-2-one 
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    | Drug-Induced Toxicity Related Proteins | 
    
      DIGOXIN ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Caspase-3  Drug:digoxin Toxicity:oncogenesis.  [¹Ù·Î°¡±â] Replated Protein:Sodium/potassium-transporting ATPase Drug:digoxin Toxicity:mitochondrial dysfunction .  [¹Ù·Î°¡±â] Replated Protein:3-hydroxy-3-methylglutaryl-coenzyme A reductase  Drug:digoxin Toxicity:mitochondrial dysfunction .  [¹Ù·Î°¡±â] Replated Protein:Multidrug resistance protein 1 (MDR1) Drug:Digoxin Toxicity:myelosuppression.  [¹Ù·Î°¡±â] 
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