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1.ÁÖÈ¿´ÉÈ¿°ú: ¾Ë·¹¸£±â¼º ºñ¿°, °íÃÊ¿, µÎµå·¯±â
2.´ÙÀ½ ȯÀÚ¿¡µµ »ç¿ëÇÒ ¼ö ÀÖ´Ù. : °¡·Á¿ò¼º ÇǺÎÁúȯ(°¡·Á¿òÁõ, ½ÀÁø, ÇǺο°), Ç÷°ü¼ººÎÁ¾, °¨±â¿¡ ÀÇÇÑ Ä๰, Àçä±â, ±âħ, ÄÚ¸·Èû
[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Clemastine]
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| Related FDA Approved Drug |
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| Mechanism of Action |
Clemastine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Clemastine is a selective histamine H1 antagonist and binds to the histamine H1 receptor. This blocks the action of endogenous histamine, which subsequently leads to temporary relief of the negative symptoms brought on by histamine.
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| Pharmacology |
Clemastine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Clemastine is an antihistamine with anticholinergic (drying) and sedative side effects. Antihistamines competitively antagonize various physiological effects of histamine including increased capillary permeability and dilatation, the formation of edema, the "flare" and "itch" response, and gastrointestinal and respiratory smooth muscle constriction. Within the vascular tree, H1- receptor antagonists inhibit both the vasoconstrictor and vasodilator effects of histamine. Depending on the dose, H1- receptor antagonists can produce CNS stimulation or depression. Most antihistamines exhibit central and/or peripheral anticholinergic activity. Antihistamines act by competitively blocking H1- receptor sites. Antihistamines do not pharmacologically antagonize or chemically inactivate histamine, nor do they prevent the release of histamine.
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| Protein Binding |
Clemastine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Clemastine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
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| Absorption |
Clemastine¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed from the gastrointestinal tract.
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| Pharmacokinetics |
ClemastineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- ÃÖ´ë Ä¡·áÈ¿°ú : 5-7½Ã°£ À̳»
- Èí¼ö : À§Àå°ü¿¡¼ °ÅÀÇ 100% Èí¼ö
- ´ë»ç : °£´ë»ç
- ¼Ò½Ç : ´¢¹è¼³
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| Biotransformation |
Clemastine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Antihistamines appear to be metabolized in the liver chiefly via mono- and didemethylation and glucuronide conjugation.
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| Toxicity |
Clemastine¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral LD50 in rat and mouse is 3550 mg/kg and 730 mg/kg, respectively. Antihistamine overdosage reactions may vary from central nervous system depression to stimulation. In children, stimulation predominates initially in a syndrome which may include excitement, hallucinations, ataxia, incoordination, muscle twitching, athetosis, hyperthermia, cyanosis convulsions, tremors, and hyperreflexia followed by postictal depression and cardio-respiratory arrest. Convulsions in children may be preceded by mild depression. Dry mouth, fixed dilated pupils, flushing of the face, and fever are common. In adults, CNS depression, ranging from drowsiness to coma, is more common.
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| Drug Interactions |
Clemastine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Donepezil Possible antagonism of actionGalantamine Possible antagonism of actionRivastigmine Possible antagonism of action
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Clemastine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food.Avoid alcohol.
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| Drug Target |
[Drug Target]
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| Description |
Clemastine¿¡ ´ëÇÑ Description Á¤º¸ A histamine H1 antagonist used as the hydrogen fumarate in hay fever, rhinitis, allergic skin conditions, and pruritus. It causes drowsiness. [PubChem]
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| Dosage Form |
Clemastine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Tablet Oral
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| Drug Category |
Clemastine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Allergic AgentsAntipruriticsHistamine H1 Antagonists
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| Smiles String Canonical |
Clemastine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CN1CCCC1CCOC(C)(C1=CC=CC=C1)C1=CC=C(Cl)C=C1
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| Smiles String Isomeric |
Clemastine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CN1CCC[C@@H]1CCO[C@](C)(C1=CC=CC=C1)C1=CC=C(Cl)C=C1
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| InChI Identifier |
Clemastine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C21H26ClNO/c1-21(17-7-4-3-5-8-17,18-10-12-19(22)13-11-18)24-16-14-20-9-6-15-23(20)2/h3-5,7-8,10-13,20H,6,9,14-16H2,1-2H3/t20-,21-/m1/s1
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| Chemical IUPAC Name |
Clemastine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2R)-2-[2-[(1R)-1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methylpyrrolidine
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ÃÖ±ÙÁ¤º¸¼öÁ¤ÀÏ 2017-07-04
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º» ¼öÁ¤ÀÏ Á¤º¸´Â Çã°¡Á¤º¸ ÀÌ¿ÜÀÇ ±âŸÁ¤º¸ ¼öÁ¤ÀÏÀ» ÀǹÌÇϹǷÎ, Çã°¡Á¤º¸¼öÁ¤ÀÏÀº º»¹®¿¡ Ç¥±âµÈ ³¯Â¥¸¦ ÂüÁ¶ÇϽñ⠹ٶø´Ï´Ù.
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»ó¼¼Á¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×À» Åä´ë·Î ÀÛ¼ºµÇ¾úÀ¸¸ç ¿ä¾àÁ¤º¸´Â »ó¼¼Á¤º¸ ¹× ±âŸ¹®ÇåÀ» ±â¹ÝÀ¸·Î µå·°ÀÎÆ÷¿¡¼ ÆíÁýÇÑ ³»¿ëÀÔ´Ï´Ù. Á¦Ç°Çã°¡»çÇ×ÀÇ ¸ñÂ÷¿Í ´Ù¼Ò »óÀÌÇÒ ¼ö ÀÖ½À´Ï´Ù. |
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°æ°í |
µå·°ÀÎÆ÷ ÀǾàÇмúÁ¤º¸´Â ½ÄǰÀǾàǰ¾ÈÀüóÀÇ Á¦Ç°Çã°¡»çÇ×, Çмú¹®Çå, Á¦¾àȸ»ç Á¦°øÁ¤º¸ µîÀ» ±Ù°Å·Î ÀÛ¼ºµÈ Âü°í Á¤º¸ÀÔ´Ï´Ù.
Á¤º¸ÀÇ Á¤È®¼ºÀ» À§ÇØ ³ë·ÂÇϰí ÀÖÀ¸³ª ÆíÁý»óÀÇ ¿À·ù, Çã°¡»çÇ× º¯°æ, Ãß°¡ÀûÀÎ Çмú¿¬±¸ ¶Ç´Â Àӻ󿬱¸ ¹ßÇ¥ µîÀ¸·Î ÀÎÇØ ¹ß»ýÇÏ´Â ¹®Á¦¿¡ ´ëÇØ µå·°ÀÎÆ÷´Â
Ã¥ÀÓÀ» ÁöÁö ¾Ê½À´Ï´Ù. ÀÚ¼¼ÇÑ ³»¿ëÀº ¡°Ã¥ÀÓÀÇ ÇÑ°è ¹× ¹ýÀû°íÁö¡±¸¦ ÂüÁ¶ÇØ ÁֽʽÿÀ.
¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù.
ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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