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    | Mechanism of Action | 
    
       Metoclopramide¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Metoclopramide inhibits gastric smooth muscle relaxation produced by dopamine, therefore increasing cholinergic response of the gastrointestinal smooth muscle. It accelerates intestinal transit and gastric emptying by preventing relaxation of gastric body and increasing the phasic activity of antrum. Simultaneously, this action is accompanied by relaxation of the upper small intestine, resulting in an improved coordination between the body and antrum of the stomach and the upper small intestine. Metoclopramide also decreases reflux into the esophagus by increasing the resting pressure of the lower esophageal sphincter and improves acid clearance from the esophagus by increasing amplitude of esophageal peristaltic contractions. Metoclopramide's dopamine antagonist action raises the threshold of activity in the chemoreceptor trigger zone and decreases the input from afferent visceral nerves. Studies have also shown that high doses of metoclopramide can antagonize 5-hydroxytryptamine (5-HT) receptors in the peripheral nervous system in animals. 
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    | Pharmacology | 
     
       Metoclopramide¿¡ ´ëÇÑ Pharmacology Á¤º¸ Metoclopramide, although chemically related to procainamide, does not possess local anesthetic or antiarrhythmic properties. Metoclopramide is used to enhance GI motility, to treat diabetic gastroparesis, as an antinauseant, and to facilitate intubation of the small bowel during radiologic examination. Metoclopramide may be used to treat chemotherapy-induced emesis and as a radiosensitizing agents in the treatment of non-small cell lung carcinoma and glioblastomas in the future. 
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    | Absorption | 
    
       Metoclopramide¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly and well absorbed (oral bioavailability 80¡¾15.5%). 
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    | Pharmacokinetics | 
    
       Metoclopramide HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
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    | Toxicity | 
    
       Metoclopramide¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral, mouse LD50: 280 mg/kg. Signs of overdose include drowsiness, disorientation, and extrapyramidal reactions. 
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    | Drug Interactions | 
    
       Metoclopramide¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Atovaquone	The agent decreases the effect of atovaquoneCyclosporine	Metoclopramide increases serum levels of cyclosporineLevodopa	Levodopa decreases the effect of metoclopramideSuccinylcholine	The agent increases the effect of succinylcholineVenlafaxine	Possible serotoninergic syndrome with this combination 
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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 | 
    
       Metoclopramide¿¡ ´ëÇÑ Description Á¤º¸ A dopamine D2 antagonist that is used as an antiemetic. [PubChem] 
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    | Dosage Form | 
    
       Metoclopramide¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Liquid	IntramuscularLiquid	IntravenousLiquid	OralTablet	Oral 
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    | Drug Category | 
    
       Metoclopramide¿¡ ´ëÇÑ Drug_Category Á¤º¸ AntiemeticsDopamine AntagonistsProkinetic Agents 
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    | Smiles String Canonical | 
    
       Metoclopramide¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN(CC)CCNC(=O)C1=CC(Cl)=C(N)C=C1OC 
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    | Smiles String Isomeric | 
    
       Metoclopramide¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN(CC)CCNC(=O)C1=CC(Cl)=C(N)C=C1OC 
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    | InChI Identifier | 
    
       Metoclopramide¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C14H22ClN3O2/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3/h8-9H,4-7,16H2,1-3H3,(H,17,19)/f/h17H 
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    | Chemical IUPAC Name | 
    
       Metoclopramide¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-amino-5-chloro-N-(2-diethylaminoethyl)-2-methoxybenzamide 
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