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°õ¸¶Æ¿200¹Ð¸®±×¶÷Á¤(¼³ÇǸ®µå)(¼öÃâ¿ë) GOMMATIL TAB.200mg
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641600070[A04302421]
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| Æ÷À塤À¯Åë´ÜÀ§ |
10, 50, 100 ,500Á¤ |
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30 Á¤ |
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8806416000700 |
8806416000717 |
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233401ATB
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| Off-label Usage |
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| Mechanism of Action |
Sulpiride¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ In contrast to most other neuroleptics which block both dopamine D1 and D2 receptors, Sulpiride is more selective and acts primarily as a dopamine D2 antagonist. Sulpiride appears to lack effects on norepinephrine, acetylcholine, serotonin, histamine, or gamma-aminobutyric acid (GABA) receptors.
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| Pharmacology |
Sulpiride¿¡ ´ëÇÑ Pharmacology Á¤º¸ Sulpiride is a substituted benzamide derivative and a selective dopamine D2 antagonist with antipsychotic and antidepressant activity. Other benzamide derivatives include metoclopramide, tiapride, and sultopride.
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| Metabolism |
Sulpiride¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Sulpiride¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Sulpiride¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 6 to 8 hours
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| Absorption |
Sulpiride¿¡ ´ëÇÑ Absorption Á¤º¸ Sulpiride is absorbed slowly from the gastrointestinal tract. Its oral bioavailability is only 25 to 35% with marked interindividual differences.
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| Pharmacokinetics |
SulpirideÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : À§Àå°üÀ¸·ÎºÎÅÍ ¼¼È÷, ÀûÀº ¾çÀÌ Èí¼öµÊ
- »ýü³»ÀÌ¿ë·ü : 27-34%
- ºÐÆ÷ : ºÐÆ÷¿ëÀû : Á¤¸ÆÁÖ»ç : 1-2.7 L/kg
- ´ë»ç : ´ë»ç¸¦ °ÅÀÇ ¹ÞÁö ¾ÊÀ½
- ¹Ý°¨±â : 6-8 ½Ã°£ (½ÅÀå¾Ö½Ã ¿¬ÀåµÊ)
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 2-6 ½Ã°£
- ¼Ò½Ç : ¹Ìº¯Èü·Î ´¢ (°æ±¸ Åõ¿©½Ã 15-30%, Á¤¸ÆÁÖ»ç½Ã 70-90%) ¹× ´ëº¯ (ƯÈ÷ °æ±¸ Åõ¿©½Ã¿¡ ¸¹Àº ¾çÀÌ)À¸·Î ¹è¼³µÊ
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| Biotransformation |
Sulpiride¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Toxicity |
Sulpiride¿¡ ´ëÇÑ Toxicity Á¤º¸ Sulpiride has a relatively low order of acute toxicity. Substantial amounts may cause severe but reversible dystonic crises with torticollis, protrusion of the tongue, and/or trism. In some cases all the classical symptoms typical of severe Parkinson's Disease may be noted; in others, over-sedation/coma may occur.
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| Drug Interactions |
Sulpiride¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Sulpiride¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available
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| Drug Target |
[Drug Target]
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| Description |
Sulpiride¿¡ ´ëÇÑ Description Á¤º¸ A dopamine D2-receptor antagonist. It has been used therapeutically as an antidepressant, antipsychotic, and as a digestive aid. (From Merck Index, 11th ed)
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| Drug Category |
Sulpiride¿¡ ´ëÇÑ Drug_Category Á¤º¸ AntidepressantsAntidepressive Agents, Second-GenerationAntipsychotic AgentsAntipsychoticsDopamine Antagonists
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| Smiles String Canonical |
Sulpiride¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCN1CCCC1CNC(=O)C1=C(OC)C=CC(=C1)S(N)(=O)=O
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| Smiles String Isomeric |
Sulpiride¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCN1CCC[C@H]1CNC(=O)C1=C(OC)C=CC(=C1)S(N)(=O)=O
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| InChI Identifier |
Sulpiride¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H23N3O4S/c1-3-18-8-4-5-11(18)10-17-15(19)13-9-12(23(16,20)21)6-7-14(13)22-2/h6-7,9,11H,3-5,8,10H2,1-2H3,(H,17,19)(H2,16,20,21)/f/h17H,16H2
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| Chemical IUPAC Name |
Sulpiride¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ N-[(1-ethylpyrrolidin-2-yl)methyl]-2-methoxy-5-sulfamoylbenzamide
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