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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: LEVOCABASTINE HYDROCHLORIDELIVOSTIN (LEVOCABASTINE HYDROCHLORIDE)
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ÀüüÀӽŠ±â°£º°·Î ¿©·¯µî±ÞÀÌ Á¸ÀçÇÒ ¼ö ÀÖÀ¸¸ç °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ º¸¿©Áý´Ï´Ù. ´Ü, º¹ÇÕÁ¦ÀÇ °æ¿ì ¸ðµç º¹ÇÕÁ¦¼ººÐ¿¡ ´ëÇÑ ÀÓºÎÅõ¿©µî±ÞÀÌ Ç¥½ÃµÈ°ÍÀº Àý´ë ¾Æ´Ï¸ç Ç¥½ÃµÈ°ÍÁß¿¡ °¡Àå À§Çèµµ°¡ ³ôÀº Á¤º¸¸¸ ³ªÅ¸³³´Ï´Ù.
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 FDA : Cµî±Þ
(levocabastine; )
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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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¹Ýµå½Ã °ø½Å·Â ÀÖ´Â ¹®ÇåÀ» ´Ù½Ã Çѹø Âü°í ÇϽñ⠹ٶó¸ç ÀÇ»ç ¶Ç´Â ¾à»çÀÇ ÆÇ´Ü¿¡ µû¶ó Åõ¿©¿©ºÎ°¡ °áÁ¤µÇ¾î¾ß ÇÕ´Ï´Ù.
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
º´¿ë±Ý±â :
°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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| Mechanism of Action |
Levocabastine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Levocabastine is a potent, selective histamine H1-receptor antagonist. It works by competing with histamine for H1-receptor sites on effector cells. It thereby prevents, but does not reverse, responses mediated by histamine alone. Levocabastine does not block histamine release but, rather, prevents histamine binding and activity. Levocabastine also binds neurotensin 2 receptors and serves as a neurotensin agonist. This can induce some degree of analgesia.
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| Pharmacology |
Levocabastine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Levocabastine is a selective histamine H1-receptor antagonist exerting inhibitory effects on the release of chemical mediators from mast cells and on the chemotaxis of polymorphonuclear leukocytes and eosinophils. Both histamine and antigens induced conjunctivitis can be inhibited by levocabastine. Levocabastine can also reduce symptoms of allergic rhinitis by preventing an increase in vascular permeability of nasal mucosa.
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| Metabolism |
Levocabastine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Levocabastine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Levocabastine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 36 hours (after oral administration)
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| Absorption |
Levocabastine¿¡ ´ëÇÑ Absorption Á¤º¸ After instillation in the eye, levocabastine is systemically absorbed, albeit at low levels.
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| Pharmacokinetics |
Levocabastine HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : ±¹¼ÒÁ¡¾ÈÀ¸·Î Àü½ÅÀûÀ¸·Î Èí¼öµÊ
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| Biotransformation |
Levocabastine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Mostly unchanged. 10 to 20% is metabolized to the acylglucuronide of levocabastine.
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| Toxicity |
Levocabastine¿¡ ´ëÇÑ Toxicity Á¤º¸ Adverse effects include visual disturbances, dry mouth, cough, nausea, eyelid edema and lacrimation.
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| Drug Interactions |
Levocabastine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Drug Target |
[Drug Target]
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| Description |
Levocabastine¿¡ ´ëÇÑ Description Á¤º¸ Levocabastine is a selective second-generation H1-receptor antagonist used for allergic conjunctivitis. Levocabastine was discovered at Janssen Pharmaceutica in 1979.
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| Dosage Form |
Levocabastine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Solution / drops OphthalmicSuspension Nasal
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| Drug Category |
Levocabastine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Histamine H1 AntagonistsHistamine H1 Antagonists, Non-Sedating
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| Smiles String Canonical |
Levocabastine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1CN(CCC1(C(O)=O)C1=CC=CC=C1)C1CCC(CC1)(C
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| Smiles String Isomeric |
Levocabastine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@@H]1CN(CC[C@]1(C(O)=O)C1=CC=CC=C1)[C@H]1CC[C@](CC1)(C
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| InChI Identifier |
Levocabastine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C26H29FN2O2/c1-19-17-29(16-15-26(19,24(30)31)21-5-3-2-4-6-21)23-11-13-25(18-28,14-12-23)20-7-9-22(27)10-8-20/h2-10,19,23H,11-17H2,1H3,(H,30,31)/t19-,23?,25?,26-/m1/s1/f/h30H
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| Chemical IUPAC Name |
Levocabastine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (3S,4R)-1-[4-cyano-4-(4-fluorophenyl)cyclohexyl]-3-methyl-4-phenylpiperidine-4-carboxylic acid
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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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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