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       Trimethobenzamide¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The mechanism of action of trimethobenzamide as determined in animals is obscure, but may involve the chemoreceptor trigger zone (CTZ), an area in the medulla oblongata through which emetic impulses are conveyed to the vomiting center; direct impulses to the vomiting center apparently are not similarly inhibited. 
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       Trimethobenzamide¿¡ ´ëÇÑ Pharmacology Á¤º¸ Trimethobenzamide is a novel antiemetic which prevents nausea and vomiting in humans. Its actions are unclear but most likely involves the chemoreceptor trigger zone (CTZ). In dogs pretreated with trimethobenzamide HCl, the emetic response to apomorphine is inhibited, while little or no protection is afforded against emesis induced by intragastric copper sulfate. 
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    | Half-life | 
    
       Trimethobenzamide¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ The mean elimination half-life of trimethobenzamide is 7 to 9 hours. 
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    | Absorption | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Absorption Á¤º¸ The relative bioavailability of the capsule formulation compared to the solution is 100%. 
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    | Pharmacokinetics | 
    
       Trimethobenzamide HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
- ÀÛ¿ë¹ßÇö½Ã°£ : 
 
-    °æ±¸ : 10-40ºÐ À̳»
 
 -    ±ÙÀ°ÁÖ»ç : 15-35ºÐ À̳»
 
 
  - ÀÛ¿ëÁö¼Ó½Ã°£ : 3-4 ½Ã°£
 
 - Èí¼ö : Á÷Àå ÁÂÁ¦ : ¾à 60%
   
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    | Biotransformation | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic. 
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    | Toxicity | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral LD50 in mice is 1600 mg/kg. 
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    | Drug Interactions | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Description | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Description Á¤º¸ Trimethobenzamide is a novel antiemetic which prevents nausea and vomiting in humans. Its actions are unclear but most likely involves the chemoreceptor trigger zone (CTZ). In dogs pretreated with trimethobenzamide HCl, the emetic response to apomorphine is inhibited, while little or no protection is afforded against emesis induced by intragastric copper sulfate. 
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    | Dosage Form | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule	OralInjection, solution	IntramuscularSuppository	Rectal 
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    | Drug Category | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antiemetics 
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    | Smiles String Canonical | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC1=CC(=CC(OC)=C1OC)C(=O)NCC1=CC=C(OCCN(C)C)C=C1 
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    | Smiles String Isomeric | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ COC1=CC(=CC(OC)=C1OC)C(=O)NCC1=CC=C(OCCN(C)C)C=C1 
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    | InChI Identifier | 
    
       Trimethobenzamide¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C21H28N2O5/c1-23(2)10-11-28-17-8-6-15(7-9-17)14-22-21(24)16-12-18(25-3)20(27-5)19(13-16)26-4/h6-9,12-13H,10-11,14H2,1-5H3,(H,22,24)/f/h22H 
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    | Chemical IUPAC Name | 
    
       Trimethobenzamide¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ N-[[4-(2-dimethylaminoethoxy)phenyl]methyl]-3,4,5-trimethoxybenzamide 
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