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8) µå¹°°Ô ÁßÁõÀÇ ½É±Ùº´Áõ, ¿ïÇ÷¼º ½ÉºÎÀü ¶Ç´Â ÃÖ±Ù ½É±Ù°æ»öÁõÀ» °ÞÀº ȯÀÚ°¡ ÀÌ ¾à°ú ÇÔ²² Á¤¸ÆÅõ¿©¿ë ¥â-¾Æµå·¹³¯¸° Â÷´ÜÁ¦ ¶Ç´Â À̼ÒÇǶó¹Ìµå¸¦ Åõ¿©¹ÞÀº °æ¿ì, ½É°¢ÇÑ ºÎÀÛ¿ëÀÌ ¹ß»ýÇß´Ù. ¾Æµå·¹³¯¸° ÀÛ¿ëÀ» °¨¼Ò½ÃŰ´Â ¾à¹°°ú ÇÔ²² ÀÌ ¾àÀ» º´¿ëÅõ¿©½Ã °úµµÇÑ ÀúÇ÷¾Ð ¹ÝÀÀÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.  
9) ½Ã¸ÞƼµò : ½Ã¸ÞƼµòÀº ÀÌ ¾àÀÇ µ¿·ÂÇп¡´Â ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê´Â´Ù. 
10) ´Ü¹éÁú °áÇÕ ¾à¹° : ÀÌ ¾àÀº Ç÷Àå ´Ü¹éÁú¿¡ °ÇÏ°Ô °áÇÕÇϹǷÎ, ´Ù¸¥ ´Ü¹éÁú °áÇÕ ¾à¹°À» Åõ¿©¹Þ´Â ȯÀÚ¿¡°Ô´Â ÁÖÀÇÇÏ¿© Åõ¿©ÇÑ´Ù. 
11) ÈíÀÔ ¸¶ÃëÁ¦ : ÈíÀÔ ¸¶ÃëÁ¦¿Í ÇÔ²² ÀÌ ¾à°ú °°Àº Ä®½· ±æÇ×Á¦¸¦ º´¿ëÅõ¿©½Ã °úµµÇÑ ½ÉÇ÷°ü ¾ïÁ¦¸¦ ÇÇÇϱâ À§ÇØ ÁÖÀÇÇÏ¿© °¢°¢ÀÇ ¾à¹° ¿ë·®À» Á¶ÀýÇÑ´Ù. 
12) ½Å°æ±ÙÂ÷´ÜÁ¦ : ÀÓ»ó ½ÇÇè ¹× µ¿¹° ½ÇÇè¿¡¼ ÀÌ ¾àÀº ½Å°æ±ÙÂ÷´ÜÁ¦(Å¥¶ó·¹ °°Àº Å»ºÐ±Ø¼º ¾à¹°)ÀÇ È°µ¿À» Áõ°½Ãų ¼öµµ ÀÖ´Ù°í º¸°íµÇ¾î Áö°í ÀÖ´Ù. º´¿ëÅõ¿©½Ã ÀÌ ¾à ¹×/¶Ç´Â ½Å°æ±ÙÂ÷´ÜÁ¦ÀÇ ¿ë·®À» °¨·®ÇÏ´Â °ÍÀÌ ÇÊ¿äÇÏ´Ù. 
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15) ½ÎÀÌŬ·Î½ºÆ÷¸° : ÀÌ ¾àÀº ½ÎÀÌŬ·Î½ºÆ÷¸°ÀÇ Ç÷Áß ³óµµ¸¦ Áõ°¡½Ãų ¼ö ÀÖ´Ù. 
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    Verapamil¿¡ ´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 | 
    
       Verapamil¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Possibly by deforming the channel, inhibiting ion-control gating mechanisms, and/or interfering with the release of calcium from the sarcoplasmic reticulum, verapamil, like diltiazem, inhibits the influx of extracellular calcium across both the myocardial and vascular smooth muscle cell membranes. The resultant inhibition of the contractile processes of the myocardial smooth muscle cells leads to dilation of the coronary and systemic arteries,improved oxygen delivery to the myocardial tissue, and decreased total peripheral resistance, systemic blood pressure, and afterload. 
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    | Pharmacology | 
     
       Verapamil¿¡ ´ëÇÑ Pharmacology Á¤º¸ Verapamil, a class IV antiarrhythmic agent, is used as a calcium-channel blocking (CCB) agent for the treatment of angina, hypertension, and for supraventricular tachyarrhythmias. 
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    | Metabolism | 
    
       Verapamil¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A2 (CYP1A2)Cytochrome P450 3A5 (CYP3A5) 
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    | Protein Binding | 
    
       Verapamil¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 90% 
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    | Half-life | 
    
       Verapamil¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2.8-7.4 hours 
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    | Absorption | 
    
       Verapamil¿¡ ´ëÇÑ Absorption Á¤º¸ 90% 
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    | Pharmacokinetics | 
    
       Verapamil HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
	- °æ±¸¿ë ºñ¼¹æÇü Á¤Á¦ 
	
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	 - ´Ü¹é°áÇÕ : 90%
	
 - ´ë»ç : °£¿¡¼ ´ë»çµÇ¸ç ÃÊȸÅë°úÈ¿°ú Å.
	
 - »ýü³»ÀÌ¿ëÀ² : °æ±¸ : 20-30%
	
 - ¹Ý°¨±â  
	
		-  ¿µ¾Æ : 4.4-6.9 ½Ã°£
		
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	 - ¼Ò½Ç : ¿ë·®ÀÇ 70%°¡ ´¢¸¦ ÅëÇØ (3-4%´Â ¹Ìº¯Èü·Î), 16%´Â ´ëº¯À¸·Î ¹è¼³µÊ.
  
 
	 
	 
	
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    | Biotransformation | 
    
       Verapamil¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available 
     | 
   
  
   
    | Toxicity | 
    
       Verapamil¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=8 mg/kg (i.v. in mice) 
     | 
   
  
   
    | Drug Interactions | 
    
       Verapamil¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
     | 
   
  
   
    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] Verapamil¿¡ ´ëÇÑ P450 table
  SUBSTRATES 
CYP 3A4/3A5/3A7 
Macrolide antibiotics: 
clarithromycin 
erythromycin 
NOT azithromycin 
telithromycin 
Anti-arrhythmics: 
quinidine 
Benzodiazepines: 
alprazolam 
diazepam 
midazolam 
triazolam 
Immune Modulators: 
cyclosporine 
tacrolimus (FK506) 
HIV Protease Inhibitors: 
indinavir 
ritonavir 
saquinavir 
Prokinetic: 
cisapride 
Antihistamines: 
astemizole 
chlorpheniramine 
Calcium Channel Blockers: 
amlodipine 
diltiazem 
felodipine 
nifedipine 
nisoldipine 
nitrendipine 
**verapamil** 
HMG CoA Reductase Inhibitors: 
atorvastatin 
cerivastatin 
lovastatin 
NOT pravastatin 
simvastatin 
aripiprazole 
buspirone 
gleevec 
haloperidol (in part) 
methadone 
pimozide 
quinine 
NOT rosuvastatin 
sildenafil 
tamoxifen 
trazodone 
vincristine 
 INHIBITORS 
CYP 3A4/3A5/3A7 
HIV Protease Inhibitors: 
indinavir 
nelfinavir 
ritonavir 
amiodarone 
NOT azithromycin 
cimetidine 
clarithromycin 
diltiazem 
erythromycin 
fluvoxamine 
grapefruit juice 
itraconazole 
ketoconazole 
mibefradil 
nefazodone 
troleandomycin 
**verapamil** 
 INDUCERS 
CYP 3A4/3A5/3A7 
carbamazepine 
phenobarbital 
phenytoin 
rifabutin 
rifampin 
St. John's wort 
troglitazone 
  SUBSTRATES 
CYP 3A4/3A5/3A7 
Macrolide antibiotics: 
clarithromycin 
erythromycin 
NOT azithromycin 
telithromycin 
Anti-arrhythmics: 
quinidine 
Benzodiazepines: 
alprazolam 
diazepam 
midazolam 
triazolam 
Immune Modulators: 
cyclosporine 
tacrolimus (FK506) 
HIV Protease Inhibitors: 
indinavir 
ritonavir 
saquinavir 
Prokinetic: 
cisapride 
Antihistamines: 
astemizole 
chlorpheniramine 
Calcium Channel Blockers: 
amlodipine 
diltiazem 
felodipine 
nifedipine 
nisoldipine 
nitrendipine 
**verapamil** 
HMG CoA Reductase Inhibitors: 
atorvastatin 
cerivastatin 
lovastatin 
NOT pravastatin 
simvastatin 
aripiprazole 
buspirone 
gleevec 
haloperidol (in part) 
methadone 
pimozide 
quinine 
NOT rosuvastatin 
sildenafil 
tamoxifen 
trazodone 
vincristine 
 INHIBITORS 
CYP 3A4/3A5/3A7 
HIV Protease Inhibitors: 
indinavir 
nelfinavir 
ritonavir 
amiodarone 
NOT azithromycin 
cimetidine 
clarithromycin 
diltiazem 
erythromycin 
fluvoxamine 
grapefruit juice 
itraconazole 
ketoconazole 
mibefradil 
nefazodone 
troleandomycin 
**verapamil** 
 INDUCERS 
CYP 3A4/3A5/3A7 
carbamazepine 
phenobarbital 
phenytoin 
rifabutin 
rifampin 
St. John's wort 
troglitazone 
     | 
   
  
   
    | Food Interaction | 
    
       Verapamil¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take with food.Avoid excessive quantities of coffee or tea (Caffeine).Avoid taking with grapefruit juice.Avoid natural licorice. 
     | 
   
  
   
    | Drug Target | 
    
      
      [Drug Target]
     | 
   
  
   
    | Description | 
    
       Verapamil¿¡ ´ëÇÑ Description Á¤º¸ A calcium channel blocker that is a class IV anti-arrhythmia agent. [PubChem] 
     | 
   
  
   
    | Dosage Form | 
    
       Verapamil¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule, extended release	OralLiquid	IntravenousSolution	IntravenousTablet	OralTablet, extended release	Oral 
     | 
   
  
   
    | Drug Category | 
    
       Verapamil¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Arrhythmia AgentsAntiarrhythmic AgentsCalcium Channel BlockersCalcium-channel blocking agentsVasodilator Agents 
     | 
   
  
   
    | Smiles String Canonical | 
    
       Verapamil¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC1=C(OC)C=C(CCN(C)CCCC(C 
     | 
   
  
   
    | Smiles String Isomeric | 
    
       Verapamil¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ COC1=C(OC)C=C(CCN(C)CCC[C@@](C 
     | 
   
  
   
    | InChI Identifier | 
    
       Verapamil¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C27H38N2O4/c1-20(2)27(19-28,22-10-12-24(31-5)26(18-22)33-7)14-8-15-29(3)16-13-21-9-11-23(30-4)25(17-21)32-6/h9-12,17-18,20H,8,13-16H2,1-7H3 
     | 
   
  
   
    | Chemical IUPAC Name | 
    
       Verapamil¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-(3,4-dimethoxyphenyl)-5-[2-(3,4-dimethoxyphenyl)ethyl-methylamino]-2-propan-2-ylpentanenitrile 
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                          ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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