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| Related FDA Approved Drug |
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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8806495048402 |
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Ç×È÷½ºÅ¸¹Î & Ç׾˷¯Áö¾à (Antihistamines & antiallergics)
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Promethazine / R06AD02
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141 (Ç×È÷½ºÅ¸¹ÎÁ¦ )
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Á¦Ç°±Ô°Ý: /Á¦Ç°¼ö·®: 0/Á¦Çü:
Æû¸ñ±âÁØÄÚµå: 199303264 /´ëÇ¥ÄÚµå: 8806495048402/Ç¥ÁØÄÚµå: 8806495048402
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(promethazine; )
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| Mechanism of Action |
Promethazine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Like other H1-antagonists, promethazine competes with free histamine for binding at H1-receptor sites in the GI tract, uterus, large blood vessels, and bronchial muscle. The relief of nausea appears to be related to central anticholinergic actions and may implicate activity on the medullary chemoreceptor trigger zone.
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| Pharmacology |
Promethazine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Promethazine, a phenothiazine, is an H1-antagonist with anticholinergic, sedative, and antiemetic effects and some local anesthetic properties. Promethazine is used as an antiemetic or to prevent motion sickness.
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| Metabolism |
Promethazine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2D6 (CYP2D6)
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| Protein Binding |
Promethazine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 93%
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| Half-life |
Promethazine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 16-19 hours
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| Absorption |
Promethazine¿¡ ´ëÇÑ Absorption Á¤º¸ On average, 88% of a promethazine dose is absorbed after oral administration; however, the absolute bioavailability is only 25% because of first-pass clearance.
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| Pharmacokinetics |
Promethazine HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- È¿°ú¹ßÇö½Ã°£ (I.V.) : 20ºÐ À̳» (3-5ºÐ)
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| Biotransformation |
Promethazine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic
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| Toxicity |
Promethazine¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include mild depression of the central nervous system and cardiovascular system to profound hypotension, respiratory depression, unconsciousness, and sudden death. Other reported reactions include hyperreflexia, hypertonia, ataxia, athetosis, and extensor-plantar reflexes (Babinski reflex). LD50=55mg/kg (I.V. in mice)
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| Drug Interactions |
Promethazine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Amphetamine Decreased anorexic effect, may increase pyschotic symptomsBenzphetamine Decreased anorexic effect, may increase pyschotic symptomsBromocriptine The phenothiazine decreases the effect of bromocriptineDextroamphetamine Decreased anorexic effect, may increase pyschotic symptomsDexfenfluramine Decreased anorexic effect, may increase pyschotic symptomsDiethylpropion Decreased anorexic effect, may increase pyschotic symptomsFenfluramine Decreased anorexic effect, may increase pyschotic symptomsGuanethidine The agent decreases the effect of guanethidineMazindol Decreased anorexic effect, may increase pyschotic symptomsMethamphetamine Decreased anorexic effect, may increase pyschotic symptomsMetrizamide Increased risk of convulsionsPhendimetrazine Decreased anorexic effect, may increase pyschotic symptomsPhenmetrazine Decreased anorexic effect, may increase pyschotic symptomsPhentermine Decreased anorexic effect, may increase pyschotic symptomsPhenylpropanolamine Decreased anorexic effect, may increase pyschotic symptomsGalantamine Possible antagonism of actionRivastigmine Possible antagonism of actionDonepezil Possible antagonism of actionSparfloxacin Increased risk of cardiotoxicity and arrhythmiasTerfenadine Increased risk of cardiotoxicity and arrhythmiasLevofloxacin Increased risk of cardiotoxicity and arrhythmiasGatifloxacin Increased risk of cardiotoxicity and arrhythmiasGrepafloxacin Increased risk of cardiotoxicity and arrhythmiasCisapride Increased risk of cardiotoxicity and arrhythmias
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Promethazine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation. Avoid alcohol.
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| Drug Target |
[Drug Target]
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| Description |
Promethazine¿¡ ´ëÇÑ Description Á¤º¸ A phenothiazine derivative with histamine H1-blocking, antimuscarinic, and sedative properties. It is used as an antiallergic, in pruritus, for motion sickness and sedation, and also in animals. [PubChem]
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| Dosage Form |
Promethazine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Cream TopicalLiquid IntramuscularSolution IntravenousSyrup OralTablet Oral
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| Drug Category |
Promethazine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Allergic AgentsAntipruriticsHistamine H1 AntagonistsPhenothiazine Derivatives
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| Smiles String Canonical |
Promethazine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(CN1C2=CC=CC=C2SC2=CC=CC=C12)N(C)C
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| Smiles String Isomeric |
Promethazine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@H](CN1C2=CC=CC=C2SC2=CC=CC=C12)N(C)C
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| InChI Identifier |
Promethazine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C17H20N2S/c1-13(18(2)3)12-19-14-8-4-6-10-16(14)20-17-11-7-5-9-15(17)19/h4-11,13H,12H2,1-3H3
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| Chemical IUPAC Name |
Promethazine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ N,N-dimethyl-1-phenothiazin-10-ylpropan-2-amine
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