| Ç׸ñ |
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
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[»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]
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|
| µ¶¼ºÁ¤º¸ |
Glycerin¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Nitroglycerin¿¡ ´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 |
Nitroglycerin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Similar to other nitrites and organic nitrates, nitroglycerin is converted to nitric oxide (NO), an active intermediate compound which activates the enzyme guanylate cyclase. This stimulates the synthesis of cyclic guanosine 3',5'-monophosphate (cGMP) which then activates a series of protein kinase-dependent phosphorylations in the smooth muscle cells, eventually resulting in the dephosphorylation of the myosin light chain of the smooth muscle fiber. The subsequent release of calcium ions results in the relaxation of the smooth muscle cells and vasodilation.
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| Pharmacology |
Nitroglycerin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Nitroglycerin, an organic nitrate, is available in many forms as a vasodilator. Nitroglycerin is used in the treatement of angina pectoris and perioperative hypertension, to produce controlled hypotension during surgical procedures, to treat hypertensive emergencies, and to treat congestive heart failure associated with myocardial infarction.
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| Metabolism |
Nitroglycerin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Nitroglycerin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Nitroglycerin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 3 minutes
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| Absorption |
Nitroglycerin¿¡ ´ëÇÑ Absorption Á¤º¸ Not Available
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| Pharmacokinetics |
NitroglycerinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ë¹ßÇö½Ã°£ ¹× ÀÛ¿ëÁö¼Ó½Ã°£ : Á¦Çü¿¡ µû¶ó ´Ù¸§

- ´Ü¹é°áÇÕ : 60%
- ´ë»ç : ÃÊȸÅë°úÈ¿°ú Å
- ¹Ý°¨±â : 1-4ºÐ
- ¼Ò½Ç : ´¢¸¦ ÅëÇØ ºñȰ¼ºÇü ´ë»çü·Î ¹è¼³
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| Biotransformation |
Nitroglycerin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic, cytochrome P450 (P450) is a key enzyme of organic nitrate biotransformation
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| Toxicity |
Nitroglycerin¿¡ ´ëÇÑ Toxicity Á¤º¸ Increased intracranial pressure, with any or all of persistent throbbing headache, confusion, and moderate fever; Vertigo; Palpitations; Visual disturbances; Nausea and vomiting (possibly with colic and even bloody diarrhea); Syncope (especially in the upright posture); Air hunger and dyspnea, later followed by reduced ventilatory effort; Diaphoresis, with the skin either flushed or cold and clammy; Heart block and bradycardia; Paralysis; Coma; Seizures; Death.
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| Drug Interactions |
Nitroglycerin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Alteplase IV nitroglycerin decreases the effect of alteplaseDihydroergotamine Possible antagonism of actionDihydroergotoxine Possible antagonism of actionErgonovine Possible antagonism of actionErgotamine Possible antagonism of actionMethylergonovine Possible antagonism of actionMethysergide Possible antagonism of actionSildenafil Possible significant hypotension with this combinationTadalafil Possible significant hypotension with this combinationVardenafil Possible significant hypotension with this combination
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Nitroglycerin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take on empty stomach: 1 hour before or 2 hours after meals.Dissolve under the tongue.
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| Drug Target |
[Drug Target]
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| Description |
Nitroglycerin¿¡ ´ëÇÑ Description Á¤º¸ A volatile vasodilator which relieves angina pectoris by stimulating guanylate cyclase and lowering cytosolic calcium. [PubChem]
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| Drug Category |
Nitroglycerin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Explosive AgentsNitrates and NitritesTocolytic AgentsVasodilator Agents
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| Smiles String Canonical |
Nitroglycerin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ [O-][N+](=O)OCC(CO[N+]([O-])=O)O[N+]([O-])=O
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| Smiles String Isomeric |
Nitroglycerin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ [O-][N+](=O)OCC(CO[N+]([O-])=O)O[N+]([O-])=O
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| InChI Identifier |
Nitroglycerin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C3H5N3O9/c7-4(8)13-1-3(15-6(11)12)2-14-5(9)10/h3H,1-2H2
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| Chemical IUPAC Name |
Nitroglycerin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 1,3-dinitrooxypropan-2-yl nitrate
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