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À¯ÇѺ긮ī´ÒÁö¼ÓÁ¤5mg(Ȳ»êÅ׸£ºÎÅ»¸°) BRICANYL TABS.[Terbutaline Sulfate]
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µå·°ÀÎÆ÷¿¡¼´Â ÀǾàǰ ÀÎÅÍ³Ý ÆÇ¸Å¸¦ ÇÏÁö ¾Ê½À´Ï´Ù. |
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642103480[A04503741]
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8806421034806 |
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[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Terbutaline]
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[¾ÈÀü¼º¼Óº¸] ¡Û ¹ßÇàÀÏÀÚ : 2011. 2. 18.
¡Û °ü·Ã Á¦Ç°
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µî 4°³»ç 5ǰ¸ñ(ºÙÀÓ ÂüÁ¶)
- ¼ººÐ¸í : Å׸£ºÎÅ»¸°(terbutaline hydrochloride)
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(Off-label)µÇ´Â "Å׸£ºÎÅ»¸° Á¦Á¦(ÁÖ»çÁ¦ ¹× °æ±¸Á¦)"¿¡ ´ëÇÏ¿©, ¡°Çã°¡
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| Mechanism of Action |
Terbutaline¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The pharmacologic effects of terbutaline are at least in part attributable to stimulation through beta-adrenergic receptors of intracellular adenyl cyclase, the enzyme that catalyzes the conversion of adenosine triphosphate (ATP) to cyclic AMP. Increased cyclic AMP levels are associated with relaxation of bronchial smooth muscle and inhibition of release of mediators of immediate hypersensitivity from cells, especially from mast cells.
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| Pharmacology |
Terbutaline¿¡ ´ëÇÑ Pharmacology Á¤º¸ Terbutaline is a relatively selective beta2-adrenergic bronchodilator. The pharmacologic effects of beta adrenergic agonist drugs, including terbutaline, are at least in part attributable to stimulation through beta adrenergic receptors of intracellular adenyl cyclase, the enzyme which catalyzes the conversion of adenosine triphosphate (ATP) to cyclic- 3',5'- adenosine monophosphate (c-AMP). Increased c-AMP levels are associated with relaxation of bronchial smooth muscle and inhibition of release of mediators of immediate hypersensitivity from cells, especially from mast cells.
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| Metabolism |
Terbutaline¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cholinesterase
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| Protein Binding |
Terbutaline¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ Not Available
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| Half-life |
Terbutaline¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 5.5-5.9 hours
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| Pharmacokinetics |
Terbutaline SulfateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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- ´Ü¹é°áÇÕ : 25%
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- »ýü³»ÀÌ¿ë·ü : ÇÇÇÏÁÖ»çÇÏ´Â °æ¿ì°¡ °æ±¸Åõ¿©½Ãº¸´Ù Å
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- ¼Ò½Ç : ½Å¹è¼³
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| Biotransformation |
Terbutaline¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Toxicity |
Terbutaline¿¡ ´ëÇÑ Toxicity Á¤º¸ Terbutaline Sulfate: Oral LD50(rat) = 8.7 g/kg; Oral LD50(mouse) = 205 mg/kg; Oral LD50(dog) = 1.5 g/kg; IP LD50(rat)= 220 mg/kg ; IP LD50(mouse) = 130 mg/kg; Oral LD50(rabbit) = >8 g/kg; IV LD50(mouse) = 36 mg/kg; IV LD50(dog) = 116 mg/kg; IV LD50(rabbit) = 110 mg/kg
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| Drug Interactions |
Terbutaline¿¡ ´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 |
Terbutaline¿¡ ´ëÇÑ Description Á¤º¸ A selective beta-2 adrenergic agonist used as a bronchodilator and tocolytic. [PubChem]
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| Dosage Form |
Terbutaline¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Aerosol, metered Respiratory (inhalation)
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| Drug Category |
Terbutaline¿¡ ´ëÇÑ Drug_Category Á¤º¸ Adrenergic beta-AgonistsBronchodilator AgentsSympathomimeticSympathomimeticsTocolytic Agents
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| Smiles String Canonical |
Terbutaline¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)(C)NCC(O)C1=CC(O)=CC(O)=C1
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| Smiles String Isomeric |
Terbutaline¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)(C)NC[C@H](O)C1=CC(O)=CC(O)=C1
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| InChI Identifier |
Terbutaline¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C12H19NO3/c1-12(2,3)13-7-11(16)8-4-9(14)6-10(15)5-8/h4-6,11,13-16H,7H2,1-3H3
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| Chemical IUPAC Name |
Terbutaline¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 5-[2-(tert-butylamino)-1-hydroxyethyl]benzene-1,3-diol
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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