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                    ½ºÆÄÁø¿¥Ä°¼¿  SPAZIN M CAP[Aluminum magnesium metasilicate , Scopolamine N-butylbromide]  
                    
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    239  (±âŸÀÇ ¼Òȱâ°ü¿ë¾à                                             )
      
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    º´¿ë±Ý±â :
     
	 °í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
	 
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    Magnesium¿¡ ´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 | 
    
       magnesium¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Not Available
  Scopolamine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Scopolamine acts by interfering with the transmission of nerve impulses by acetylcholine in the parasympathetic nervous system (specifically the vomiting center). 
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    | Pharmacology | 
     
       Scopolamine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Scopolamine is a muscarinic antagonist structurally similar to the neurotransmitter acetylcholine and acts by blocking the muscarinic acetylcholine receptors and is thus classified as an anticholinergic. Scopolamine has many uses including the prevention of motion sickness. It is not clear how Scopolamine prevents nausea and vomiting due to motion sickness. The vestibular part of the ear is very important for balance. When a person becomes disoriented due to motion, the vestibule sends a signal through nerves to the vomiting center in the brain, and vomiting occurs. Acetylcholine is a chemical that nerves use to transmit messages to each other. It is believe that Scopolamine prevents communication between the nerves of the vestibule and the vomiting center in the brain by blocking the action of acetylcholine. Scopolamine also may work directly on the vomiting center. Scopolamine must be taken before the onset of motion sickness to be effective. 
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    | Metabolism | 
    
       Scopolamine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available 
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    | Protein Binding | 
    
       Scopolamine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available 
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    | Half-life | 
    
       Scopolamine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available 
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    | Absorption | 
    
       Scopolamine¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available 
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    | Pharmacokinetics | 
    
       Scopolamine N-butylbromideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
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    | Biotransformation | 
    
       Scopolamine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available 
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    | Toxicity | 
    
       Scopolamine¿¡ ´ëÇÑ Toxicity Á¤º¸ Not Available 
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    | Drug Interactions | 
    
       magnesium¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Alendronate	Formation of non-absorbable complexesCiprofloxacin	Formation of non-absorbable complexesClodronate	Formation of non-absorbable complexesDemeclocycline	Formation of non-absorbable complexesDoxycycline	Formation of non-absorbable complexesEnoxacin	Formation of non-absorbable complexesEtidronic acid	Formation of non-absorbable complexesGatifloxacin	Formation of non-absorbable complexesGemifloxacin	Formation of non-absorbable complexesGrepafloxacin	Formation of non-absorbable complexesIbandronate	Formation of non-absorbable complexesLevofloxacin	Formation of non-absorbable complexesLomefloxacin	Formation of non-absorbable complexesMethacycline	Formation of non-absorbable complexesMinocycline	Formation of non-absorbable complexesMoxifloxacin	Formation of non-absorbable complexesNorfloxacin	Formation of non-absorbable complexesOfloxacin	Formation of non-absorbable complexesOxytetracycline	Formation of non-absorbable complexesPefloxacin	Formation of non-absorbable complexesRisedronate	Formation of non-absorbable complexesTrovafloxacin	Formation of non-absorbable complexesTetracycline	Formation of non-absorbable complexesTemafloxacin	Formation of non-absorbable complexesAmprenavir	The antiacid decreases the absorption of amprenavirChloroquine	The antiacid decreases the absorption of chloroquineAtazanavir	This gastric pH modifier decreases the levels/effects of atazanavirDelavirdine	The antiacid decreases the absorption of delavirdineDihydroquinidine barbiturate	The antiacid decreases the absorption of quinidineFosamprenavir	The antiacid decreases the absorption of amprenavirIndinavir	The antiacid decreases the absorption of indinavirQuinidine	The antiacid decreases the absorption of quindineQuinidine barbiturate	The antiacid decreases the absorption of quinidinePolystyrene sulfonate	Risk of alkalosis in renal impairmentRosuvastatin	The antiacid decreases the absorption of rosuvastatin
  Scopolamine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Drug Target | 
    
      
      [Drug Target]
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    | Description | 
    
       magnesium¿¡ ´ëÇÑ Description Á¤º¸ Magnesium hydroxide is used primarily in "Milk of Magnesia", a white aqueous, mildly alkaline suspension of magnesium hydroxide formulated at about 8%w/v. Milk of magnesia is primarily used to alleviate constipation, but can also be used to relieve indigestion and heartburn. When taken internally by mouth as a laxative, the osmotic force of the magnesia suspension acts to draw fluids from the body and to retain those already within the lumen of the intestine, serving to distend the bowel, thus stimulating nerves within the colon wall, inducing peristalsis and resulting in evacuation of colonic contents.
  Scopolamine¿¡ ´ëÇÑ Description Á¤º¸ An alkaloid from Solanaceae, especially Datura metel L. and Scopola carniolica. Scopolamine and its quaternary derivatives act as antimuscarinics like atropine, but may have more central nervous system effects. Among the many uses are as an anesthetic premedication, in urinary incontinence, in motion sickness, as an antispasmodic, and as a mydriatic and cycloplegic. [PubChem] 
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    | Dosage Form | 
    
       magnesium¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol	OralCapsule	OralLiquid	IntramuscularLiquid	IntravenousLiquid	OralOintment	TopicalPellet	OralPowder	OralSolution	IntramuscularSolution	IntravenousSolution	OralSolution / drops	OralSuspension	OralSyrup	OralTablet	Oral
  Scopolamine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Disc	TransdermalLiquid	IntravenousSolution	IntramuscularSolution	IntravenousTablet	Oral 
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    | Drug Category | 
    
       magnesium¿¡ ´ëÇÑ Drug_Category Á¤º¸ Not Available
  Scopolamine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AdjuvantsAdjuvants, AnesthesiaAntimuscarinicsAntispasmodicsCholinergic AntagonistsMuscarinic AntagonistsMydriatics 
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    | Smiles String Canonical | 
    
       magnesium¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ [Mg++]
  Scopolamine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1C2CC(CC1C1OC21)OC(=O)C(CO)C1=CC=CC=C1 
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    | Smiles String Isomeric | 
    
       magnesium¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ [Mg++]
  Scopolamine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1[C@H]2C[C@H](C[C@@H]1[C@H]1O[C@@H]21)OC(=O)[C@@H](CO)C1=CC=CC=C1 
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    | InChI Identifier | 
    
       magnesium¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/Mg/q+2
  Scopolamine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C17H21NO4/c1-18-13-7-11(8-14(18)16-15(13)22-16)21-17(20)12(9-19)10-5-3-2-4-6-10/h2-6,11-16,19H,7-9H2,1H3 
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    | Chemical IUPAC Name | 
    
       magnesium¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ magnesium(+2) cation
  Scopolamine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ Not Available 
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    | Drug-Induced Toxicity Related Proteins | 
    
      SILICA ÀÇ Drug-Induced Toxicity Related ProteinÁ¤º¸ Replated Protein:Nuclear factor NF-kappa-B Drug:SIlica Toxicity:pulmonary inflammation.  [¹Ù·Î°¡±â] 
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