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µ¿±¹¿°»êµµÆÄ¹ÎÁÖ»ç250mg(ÇÁ¸®Çʵå) DOPAMINE HCL 250mg INJ.[Dopamine HCl]
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Dopamine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Dopamine is a precursor to norepinephrine in noradrenergic nerves and is also a neurotransmitter in certain areas of the central nervous system. Dopamine produces positive chronotropic and inotropic effects on the myocardium, resulting in increased heart rate and cardiac contractility. This is accomplished directly by exerting an agonist action on beta-adrenoceptors and indirectly by causing release of norepinephrine from storage sites in sympathetic nerve endings.
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Dopamine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Dopamine is a natural catecholamine formed by the decarboxylation of 3,4-dihydroxyphenylalanine (DOPA). It is a precursor to norepinephrine in noradrenergic nerves and is also a neurotransmitter in certain areas of the central nervous system, especially in the nigrostriatal tract, and in a few peripheral sympathetic nerves. Dopamine produces positive chronotropic and inotropic effects on the myocardium, resulting in increased heart rate and cardiac contractility. This is accomplished directly by exerting an agonist action on beta-adrenoceptors and indirectly by causing release of norepinephrine from storage sites in sympathetic nerve endings.
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Dopamine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Monoamine oxidase type A (MAO-A)Monoamine oxidase type B (MAO-B)Catechol O-methyltransferase (COMT)
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Dopamine¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ No information currently available on protein binding.
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Dopamine¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 2 minutes
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Dopamine¿¡ ´ëÇÑ Absorption Á¤º¸ Dopamine is rapidly absorbed from the small intestine.
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| Biotransformation |
Dopamine¿¡ ´ëÇÑ Biotransformation Á¤º¸ Biotransformation of dopamine proceeds rapidly to yield the principal excretion products, 3-4-dihydroxy-phenylacetic acid (DOPAC) and 3-methoxy-4-hydroxy-phenylacetic acid (homovanillic acid, HVA).
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| Toxicity |
Dopamine¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50 oral mice = 1460 mg/kg, LD50 oral rats = 1780 mg/kg. Spasm or closing of eyelids, nausea, vomiting, cardiac arrhythmias, involuntary movements of the body including the face, tongue, arms, hand, head, and upper body; hypotension, haemolytic anaemia, urinary retention, duodenal ulcer, sialorrhea, ataxia, abdominal pain, dry mouth, nightmares, tachypnoea, bruxism, confusion, and insomnia.
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| Drug Interactions |
Dopamine¿¡ ´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 |
Dopamine¿¡ ´ëÇÑ Description Á¤º¸ One of the catecholamine neurotransmitters in the brain. It is derived from tyrosine and is the precursor to norepinephrine and epinephrine. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (receptors, dopamine) mediate its action. [PubChem]
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| Dosage Form |
Dopamine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Injection, solution, concentrate Intravenous drip
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| Drug Category |
Dopamine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Cardiotonic AgentsDopamine AgentsSympathomimeticSympathomimetics
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| Smiles String Canonical |
Dopamine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NCCC1=CC(O)=C(O)C=C1
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| Smiles String Isomeric |
Dopamine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ NCCC1=CC(O)=C(O)C=C1
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| InChI Identifier |
Dopamine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C8H11NO2/c9-4-3-6-1-2-7(10)8(11)5-6/h1-2,5,10-11H,3-4,9H2
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| Chemical IUPAC Name |
Dopamine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-(2-aminoethyl)benzene-1,2-diol
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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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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.
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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