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Ç×È÷½ºÅ¸¹Î & Ç׾˷¯Áö¾à (Antihistamines & antiallergics)
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Loratadine / R06AX13
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FDA : Bµî±Þ
(loratadine; )
*
»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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Pharmacokinetics
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Mechanism of Action
Loratadine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Like other H1 -blockers, loratadine competes with free histamine for binding at H1 -receptors in the GI tract, uterus, large blood vessels, and bronchial muscle. Loratadine also has a weak affinity for acetylcholine and alpha-adrenergic receptors.
Pharmacology
Loratadine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Loratadine, a non-sedating H1 -blocker similar in structure to cyproheptadine and azatadine, is used to treat seasonal allergic rhinitis. Unlike other H1 -blockers, loratidine does not penetrate the CNS effectively and has a low affinity for CNS H1 -receptors.
Metabolism
Loratadine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 3A4 (CYP3A4)Cytochrome P450 2C19 (CYP2C19)Cytochrome P450 2D6 (CYP2D6)
Protein Binding
Loratadine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
Half-life
Loratadine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 8.4 hours
Absorption
Loratadine¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed following oral administration (40% bioavailability)
Pharmacokinetics
LoratadineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
ÀÛ¿ë¹ßÇö½Ã°£ : 1-3 ½Ã°£ À̳»
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Èí¼ö : ½Å¼ÓÈ÷ Èí¼ö
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Biotransformation
Loratadine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic
Toxicity
Loratadine¿¡ ´ëÇÑ Toxicity Á¤º¸ somnolence, tachycardia, and headache LD50 =mg/kg (orally in rat)
Drug Interactions
Loratadine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Nefazodone Increased risk of cardiotoxicity
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Loratadine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take on empty stomach: 1 hour before or 2 hours after meals.
Drug Target
[Drug Target]
Description
Loratadine¿¡ ´ëÇÑ Description Á¤º¸ A second-generation histamine H1 receptor antagonist used in the treatment of allergic rhinitis and urticaria. Unlike most classical antihistamines (histamine H1 antagonists) it lacks central nervous system depressing effects such as drowsiness. [PubChem]
Dosage Form
÷°¡Á¦1 ¾Æ½ºÆÄŽ (°æ±¸ Á¦¿¡ ÇÑÇÔ.) ¡Ü 1ÀÏ Çã¿ë·®Á¦ÇÑ
¾Æ½ºÆÄŽ ÇÔ·®À» WHO ±ÇÀå·®(40mg/kg/1ÀÏ)dlgkfh Á¶Á¤(°¡´ÉÇÑ ÃÖ¼Ò·® »ç¿ë)ÇÒ °Í.
60kg ¼ºÀÎ : 1ÀÏ Ãִ뺹¿ë·® 24g
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Drug Category
Loratadine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Allergic AgentsAntihistaminesAntipruriticsHistamine H1 Antagonists, Non-Sedating
Smiles String Canonical
Loratadine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCOC(=O)N1CCC(CC1)=C1C2=C(CCC3=C1N=CC=C3)C=C(Cl)C=C2
Smiles String Isomeric
Loratadine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCOC(=O)N1CC\C(CC1)=C1/C2=C(CCC3=C1N=CC=C3)C=C(Cl)C=C2
InChI Identifier
Loratadine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H23ClN2O2/c1-2-27-22(26)25-12-9-15(10-13-25)20-19-8-7-18(23)14-17(19)6-5-16-4-3-11-24-21(16)20/h3-4,7-8,11,14H,2,5-6,9-10,12-13H2,1H3
Chemical IUPAC Name
Loratadine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxylic acid ethyl ester
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