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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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ÀÌ¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
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[A09202111]
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
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1. Á¤½ÅºÐ¿Áõ
2. Àú´É°ú ¸¸¼º³úÁúȯÀ¸·Î ÀÎÇÑ ÇൿÀå¾Ö
3. ±Þ¸¸¼º ¾ËÄÚ¿ÃÁßµ¶
4. Á¤½Å½Å°æÁõ
[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Mesoridazine]
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* Àý´ë ÀÓÀǺ¹¿ëÇÏÁö ¸¶½Ã°í ¹Ýµå½Ã ÀÇ»ç ¶Ç´Â ¾à»ç¿Í »ó´ãÇϽñ⠹ٶø´Ï´Ù.
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1. Á¤½ÅºÐ¿Áõ : ÃÊȸ Åõ¿©·®Àº 1ȸ 50¹Ð¸®±×¶÷ 1ÀÏ 3ȸ °æ±¸Åõ¿©.
ÀÌÈÄ ÃÖÀû 1ÀÏ Åõ¿©·®Àº 100¡400¹Ð¸®±×¶÷ÀÌ´Ù.
2. Àú´É°ú ¸¸¼º³úÁúȯÀ¸·Î ÀÎÇÑ ÇൿÀå¾Ö : ÃÊȸ Åõ¿©·®Àº 1ȸ 25¹Ð¸®±×¶÷, 1ÀÏ 3ȸ °æ±¸Åõ¿©. ÀÌÈÄ ÃÖÀû 1ÀÏ Åõ¿©·®Àº 75¡300¹Ð¸®±×¶÷ÀÌ´Ù.
3. ¾ËÄÚ¿ÃÁßµ¶ : ÃÊȸ Åõ¿©·®Àº 1ȸ 25¹Ð¸®±×¶÷, 1ÀÏ 2ȸ °æ±¸Åõ¿©.
ÀÌÈÄ ÃÖÀû1ÀÏ Åõ¿©·®Àº 50¡200¹Ð¸®±×¶÷ÀÌ´Ù.
4. Á¤½Å½Å°æÁõ : ÃÊȸ Åõ¿©·®Àº 1ȸ 10¹Ð¸®±×¶÷, 1ÀÏ 3ȸ °æ±¸Åõ¿©. ÀÌÈÄ ÃÖÀû 1ÀÏ Åõ¿©·®Àº 30¡150¹Ð¸®±×¶÷ÀÌ´Ù.
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- ÀÚÀ²½Å°æ°è :
Ãൿ, º¯ºñ, ½Ä¿åºÎÁø, ¸¶ºñ¼ºÀåÆó»ö
ÇǺιÝÀÀ : È«¹Ý, ¹ÚÅ»¼ºÇǺο°, Á¢Ã˼ºÇǺο°
Ç÷¾×°è : ¹«°ú¸³±¸Áõ, ¹éÇ÷±¸°¨¼ÒÁõ, È£»ê±¸Áõ´ÙÁõ, Ç÷¼ÒÆÇ°¨¼ÒÁõ, ºóÇ÷, Àç»ýºÒ·®¼ººóÇ÷, ¹üÇ÷±¸ °¨¼ÒÁõ
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ºñ´¢±âÀå¾Ö : ´¢Àú·ù, ´¢½Ç±Ý
±âŸ : ÀÌ»ó°í¿Áõ, ¸ð¼ø¹ÝÀÀÀ¸·Î ÃßÁ¤µÇ´Â ÇൿÀû¹ÝÀÀ(ÈïºÐ, ¾Ç¸ù, Á¤½ÅÀÌ»óÀÇ ¾ÇÈ ¹× Áßµ¶¼º Âø¶õ»óÅ µî)ÀÌ º¸°íµÇ¾úÀ¸¸ç, ÃÖ±Ù¿¡´Â Æä³ëƼ¾ÆÁø·ù Àå±â¿¬¿ëÀ¸·Î ƯÀ̼º ÇǺÎ-¾ÈÁõ»óÀÌ ¹ß°ßµÇ¾ú½À´Ï´Ù. ÀÌ ¹ÝÀÀÀº ÇǺγª °á¸·ºÎÀ§ÀÇ ÁøÇ༺ »ö¼ÒÄ§ÂøÀ¸·Î ³ªÅ¸³ª°Å³ª ¶Ç´Â ³ëÃâ°ø¸·À̳ª °¢¸·ÀÇ Å»»öÀ» ³ªÅ¸³½´Ù. °¢¸·¡¤¼öÁ¤Ã¼ ȥʵµ º¸°íµÈ ¹Ù ÀÖ´Ù. Àü½Å È«¹Ý¼º ·çǪ½º¾ç ÁõÈıº
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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: MESORIDAZINE BESYLATESERENTIL (MESORIDAZINE BESYLATE)
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»ó±â ÀÓºÎÅõ¿©¿¡ ´ëÇÑ Á¤º¸´Â Àü»êó¸® µÇ¸é¼ ÀÔ·Â ¿À·ù °¡´É¼ºÀÌ Á¸ÀçÇÕ´Ï´Ù. ¿À·ù °¡´É¼ºÀ» ÃÖ¼ÒÈÇϱâ À§ÇÏ¿© ¸¹Àº ³ë·ÂÀ» ±â¿ïÀ̰í ÀÖÀ¸³ª, ±× Á¤È®¼º¿¡ ´ëÇÏ¿© È®½ÅÀ» µå¸± ¼ö ¾ø½À´Ï´Ù. ÀÌ¿¡ ´ëÇØ ȸ»ç´Â Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù.
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| Mechanism of Action |
Mesoridazine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Based upon animal studies, mesoridazine, as with other phenothiazines, acts indirectly on reticular formation, whereby neuronal activity into reticular formation is reduced without affecting its intrinsic ability to activate the cerebral cortex. In addition, the phenothiazines exhibit at least part of their activities through depression of hypothalamic centers. Neurochemically, the phenothiazines are thought to exert their effects by a central adrenergic blocking action.
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| Pharmacology |
Mesoridazine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Mesoridazine, the besylate salt of a metabolite of thioridazine, is a phenothiazine tranquilizer. Pharmacological studies in laboratory animals have established that mesoridazine has a spectrum of pharmacodynamic actions typical of a major tranquilizer. In common with other tranquilizers it inhibits spontaneous motor activity in mice, prolongs thiopental and hexobarbital sleeping time in mice and produces spindles and block of arousal reaction in the EEG of rabbits. It is effective in blocking spinal reflexes in the cut and antagonizes d-amphetamine excitation and toxicity in grouped mice. It shows a moderate adrenergic blocking activity in vitro and in vivo and antagonizes 5-hydroxytryptamine in vivo. Intravenously administered, it lowers the blood pressure of anesthetized dogs. It has a weak antiacetylcholine effect in vitro.
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| Metabolism |
Mesoridazine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2D6 (CYP2D6)
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| Protein Binding |
Mesoridazine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 4%
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| Half-life |
Mesoridazine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 24 to 48 hours
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| Absorption |
Mesoridazine¿¡ ´ëÇÑ Absorption Á¤º¸ Well absorbed from the gastrointestinal tract.
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| Pharmacokinetics |
Mesoridazine BesylateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÀÛ¿ëÁö¼Ó½Ã°£ : 4-6 ½Ã°£
- Èí¼ö : °æ±¸ : Á¤Á¦´Â ºÒ±ÔÄ¢ÀûÀ¸·Î Èí¼öµÇ¸ç, ¾×Á¦°¡ Á¤Á¦º¸´Ù Àß Èí¼öµÊ
- ´Ü¹é°áÇÕ : 91-99%
- ¹Ý°¨±â : 24-48 ½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 2-4 ½Ã°£
- Á¤»ó»óÅ µµ´Þ½Ã°£ : 4-7ÀÏ
- ¼Ò½Ç : ½Å¹è¼³
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| Biotransformation |
Mesoridazine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Toxicity |
Mesoridazine¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral LD50 is 560 ¡¾ 62.5 mg/kg and 644 ¡¾ 48 mg/kg in mouse and rat, respectively. Symptoms of overdose may include emesis, muscle tremors, decreased food intake and death associated with aspiration of oral-gastric contents into the respiratory system.
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| Drug Interactions |
Mesoridazine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Amiodarone Increased risk of cardiotoxicity and arrhythmiasAmitriptyline Increased risk of cardiotoxicity and arrhythmiasAstemizole Increased risk of cardiotoxicity and arrhythmiasBretylium Increased risk of cardiotoxicity and arrhythmiasChloroquine Increased risk of cardiotoxicity and arrhythmiasChlorpromazine Increased risk of cardiotoxicity and arrhythmiasCisapride Increased risk of cardiotoxicity and arrhythmiasDiltiazem Increased risk of cardiotoxicity and arrhythmiasDiphenhydramine Increased risk of cardiotoxicity and arrhythmiasDisopyramide Increased risk of cardiotoxicity and arrhythmiasDofetilide Increased risk of cardiotoxicity and arrhythmiasDoxepin Increased risk of cardiotoxicity and arrhythmiasErythromycin Increased risk of cardiotoxicity and arrhythmiasFlecainide Increased risk of cardiotoxicity and arrhythmiasFluoxetine Increased risk of cardiotoxicity and arrhythmiasFluvoxamine Increased risk of cardiotoxicity and arrhythmiasGatifloxacin Increased risk of cardiotoxicity and arrhythmiasGrepafloxacin Increased risk of cardiotoxicity and arrhythmiasHalofantrine Increased risk of cardiotoxicity and arrhythmiasHaloperidol Increased risk of cardiotoxicity and arrhythmiasImipramine Increased risk of cardiotoxicity and arrhythmiasJosamycin Increased risk of cardiotoxicity and arrhythmiasLevofloxacin Increased risk of cardiotoxicity and arrhythmiasMaprotiline Increased risk of cardiotoxicity and arrhythmiasMetrizamide Increased risk of cardiotoxicity and arrhythmiasParoxetine Increased risk of cardiotoxicity and arrhythmiasPenicillin G Increased risk of cardiotoxicity and arrhythmiasPentamidine Increased risk of cardiotoxicity and arrhythmiasPimozide Increased risk of cardiotoxicity and arrhythmiasPindolol Increased risk of cardiotoxicity and arrhythmiasProcainamide Increased risk of cardiotoxicity and arrhythmiasPropafenone Increased risk of cardiotoxicity and arrhythmiasPropranolol Increased risk of cardiotoxicity and arrhythmiasQuinidine Increased risk of cardiotoxicity and arrhythmiasQuinidine barbiturate Increased risk of cardiotoxicity and arrhythmiasQuinine Increased risk of cardiotoxicity and arrhythmiasSotalol Increased risk of cardiotoxicity and arrhythmiasSertindole Increased risk of cardiotoxicity and arrhythmiasSparfloxacin Increased risk of cardiotoxicity and arrhythmiasTerfenadine Increased risk of cardiotoxicity and arrhythmiasZiprasidone Increased risk of cardiotoxicity and arrhythmiasSpiramycin Increased risk of cardiotoxicity and arrhythmiasRivastigmine Possible antagonism of actionBromocriptine The phenothiazine decreases the effect of bromocriptineDonepezil Possible antagonism of actionGalantamine Possible antagonism of actionGuanethidine The agent decreases the effect of guanethidineAmphetamine Decreased anorexic effect, may increase psychotic symptomsBenzphetamine Decreased anorexic effect, may increase psychotic symptomsDexfenfluramine Decreased anorexic effect, may increase psychotic symptomsDiethylpropion Decreased anorexic effect, may increase psychotic symptomsDextroamphetamine Decreased anorexic effect, may increase psychotic symptomsFenfluramine Decreased anorexic effect, may increase psychotic symptomsMazindol Decreased anorexic effect, may increase psychotic symptomsMethamphetamine Decreased anorexic effect, may increase psychotic symptomsPhenylpropanolamine Decreased anorexic effect, may increase psychotic symptomsPhentermine Decreased anorexic effect, may increase psychotic symptomsPhenmetrazine Decreased anorexic effect, may increase psychotic symptomsPhendimetrazine Decreased anorexic effect, may increase psychotic symptoms
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Mesoridazine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation.
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| Drug Target |
[Drug Target]
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| Description |
Mesoridazine¿¡ ´ëÇÑ Description Á¤º¸ A phenothiazine antipsychotic with effects similar to chlorpromazine. [PubChem]
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| Dosage Form |
Mesoridazine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Injection, solution IntramuscularTablet Oral
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| Drug Category |
Mesoridazine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antipsychotic AgentsAntipsychoticsDopamine AntagonistsPhenothiazines
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| Smiles String Canonical |
Mesoridazine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1CCCCC1CCN1C2=CC=CC=C2SC2=C1C=C(C=C2)S(C)=O
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| Smiles String Isomeric |
Mesoridazine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1CCCC[C@@H]1CCN1C2=CC=CC=C2SC2=C1C=C(C=C2)[S@@](C)=O
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| InChI Identifier |
Mesoridazine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C21H26N2OS2/c1-22-13-6-5-7-16(22)12-14-23-18-8-3-4-9-20(18)25-21-11-10-17(26(2)24)15-19(21)23/h3-4,8-11,15-16H,5-7,12-14H2,1-2H3
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| Chemical IUPAC Name |
Mesoridazine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 10-[2-(1-methylpiperidin-2-yl)ethyl]-2-methylsulfinylphenothiazine
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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