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1) ÀÌ ¾àÀº °ú·®Åõ¿©·Î ´ÙÀ½°ú °°Àº ºÎÀÛ¿ëÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î °¨·® ¶Ç´Â ÈÞ¾à µî ÀûÀýÇÑ Ã³Ä¡¸¦ ÇÑ´Ù.
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| º¸°ü»ó ÁÖÀÇ |
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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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Thyroxin¿¡ ´ëÇÑ µ¶¼ºÁ¤º¸ : Á¤º¸º¸±â
Ãâó: ±¹¸³µ¶¼º°úÇпø µ¶¼º¹°ÁúÁ¤º¸DB : http://www.nitr.go.kr/nitr/contents/m134200/view.do |
| Mechanism of Action |
Levothyroxine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Levothyroxine acts like the endogenous thyroid hormone thyroxine (T4, a tetra-iodinated tyrosine derivative). In the liver and kidney, T4 is converted to T3, the active metabolite. In order to increase solubility, the thyroid hormones attach to thyroid hormone binding proteins, thyroxin-binding globulin, and thyroxin-binding prealbumin (transthyretin). Transport and binding to thyroid hormone receptors in the cytoplasm and nucleus then takes place. Thus by acting as a replacement for natural thyroxine, symptoms of thyroxine deficiency are relieved.
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| Pharmacology |
Levothyroxine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Levothyroxine (T4) is a synthetically prepared levo isomer of thyroxine, the major hormone secreted from the thyroid gland. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form triiodothyronine which exerts a broad spectrum of stimulatory effects on cell metabolism. Thyroid hormone increases the metabolic rate of cells of all tissues in the body. In the fetus and newborn, thyroid hormone is important for the growth and development of all tissues including bones and the brain. In adults, thyroid hormone helps to maintain brain function, food metabolism, and body temperature, among other effects. The symptoms of thyroid deficiency relieved by levothyroxine include slow speech, lack of energy, weight gain, hair loss, dry thick skin and unusual sensitivity to cold.
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| Protein Binding |
Levothyroxine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ > 99%
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| Half-life |
Levothyroxine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 6 to 7 days
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| Absorption |
Levothyroxine¿¡ ´ëÇÑ Absorption Á¤º¸ Bioavailability varies from 48% to 80%. Human studies have confirmed the importance of an intact jejunum and ileum for levothyroxine absorption and have shown some absorption from the duodenum.
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| Biotransformation |
Levothyroxine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic (primarily via cytochrome P450 isozyme 3A4).
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| Toxicity |
Levothyroxine¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=20 mg/kg (orally in rat). Hypermetabolic state indistinguishable from thyrotoxicosis of endogenous origin. Symptoms of thyrotoxicosis include weight loss, increased appetite, palpitations, nervousness, diarrhea, abdominal cramps, sweating, tachycardia, increased pulse and blood pressure, cardiac arrhythmias, tremors, insomnia, heat intolerance, fever, and menstrual irregularities.
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| Drug Interactions |
Levothyroxine¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Anisindione Thyroid hormones increase the anticoagulant effectAcenocoumarol Thyroid hormones increase the anticoagulant effectDicumarol Thyroid hormones increase the anticoagulant effectWarfarin Thyroid hormones increase the anticoagulant effectCalcium Calcium decreases absorption of levothyroxineIron Iron decreases absorption of levothyroxineColestipol The resin decreases the absorption of thyroid hormonesCholestyramine The resin decreases the absorption of thyroid hormonesDigoxin The thyroid hormone decreases the effect of digoxinRaloxifene Raloxifene decreases absorption of levothyroxineSucralfate Sucralfate decreases the effect of levothyroxine
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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 |
Levothyroxine¿¡ ´ëÇÑ Description Á¤º¸ The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (monoiodotyrosine) and the coupling of iodotyrosines (diiodotyrosine) in the thyroglobulin. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form triiodothyronine which exerts a broad spectrum of stimulatory effects on cell metabolism. [PubChem]
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| Dosage Form |
Levothyroxine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Powder, for solution IntravenousTablet Oral
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| Drug Category |
Levothyroxine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AnticoagulantsAntithyroid Agents
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| Smiles String Canonical |
Levothyroxine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC(CC1=CC(I)=C(OC2=CC(I)=C(O)C(I)=C2)C(I)=C1)C(O)=O
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| Smiles String Isomeric |
Levothyroxine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ N[C@@H](CC1=CC(I)=C(OC2=CC(I)=C(O)C(I)=C2)C(I)=C1)C(O)=O
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| InChI Identifier |
Levothyroxine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H11I4NO4/c16-8-4-7(5-9(17)13(8)21)24-14-10(18)1-6(2-11(14)19)3-12(20)15(22)23/h1-2,4-5,12,21H,3,20H2,(H,22,23)/t12-/m0/s1/f/h22H
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| Chemical IUPAC Name |
Levothyroxine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoic 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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