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1. Åå¼ÒÇöóÁÁõ Ä¡·á: ÀÌ ¾àÀº ¼³Æù¾Æ¸¶À̵åÁ¦Á¦¿Í º´¿ëÀ¸·Î Åõ¿©½Ã »ó½ÂÈ¿°ú°¡ Àֱ⠶§¹®¿¡ Åå¼ÒÇöóÁÁõ Ä¡·á¿¡ ±ÇÀåµÈ´Ù.
2. ±Þ¼º ¸»¶ó¸®¾Æ Ä¡·á: ÀÌ ¾àÀº ±Þ¼º ¸»¶ó¸®¾Æ Ä¡·á¿¡ »ç¿ëµÈ´Ù. ±Þ¼º ¸»¶ó¸®¾Æ Ä¡·á½Ã ´Üµ¶À¸·Î »ç¿ëÇÏ¿©¼´Â ¾È µÈ´Ù. ±Þ¼º ¸»¶ó¸®¾Æ Ä¡·á ½Ã Ŭ·Î·ÎÄý ¶Ç´Â Äû´Ñ°ú °°Àº ½Å¼ÓÈ÷ ÀÛ¿ëÇÏ´Â Schizonticides°¡ »ç¿ëµÇ¸ç ¼±È£µÈ´Ù. ±×·¯³ª, ¼³Æù¾Æ¸¶À̵å(¿¹¸¦ µé¸é, ¼³ÆÄµ¶½Å)¿Í ÀÌ ¾àÀÇ º´¿ëÅõ¿©´Â ¸»¶ó¸®¾Æ¿øÃæ(Plasmodia)ÀÇ °¨¼ö¼º ÀÖ´Â Á¾ÀÇ Àü´Þ Á¶Àý°ú ¾ïÁ¦¸¦ ½ÃÀÛÇÑ´Ù.
3. ¸»¶ó¸®¾ÆÀÇ ÈÇÐÀû¿¹¹æ: ÀÌ ¾àÀº ¸»¶ó¸®¾Æ¿øÃæ(Plasmodia)ÀÇ °¨¼ö¼º ÀÖ´Â Á¾¿¡ ´ëÇÑ ¸»¶ó¸®¾ÆÀÇ ÈÇÐÀû ¿¹¹æ¿¡ »ç¿ëµÈ´Ù. ±×·¯³ª, ÇǸ®¸ÞŸ¹Î¿¡ ´ëÇÑ ³»¼ºÀº Àü¼¼°èÀûÀ¸·Î ÆÛÁ®ÀÖ´Ù. ¸ðµç Áö¿ªÀÇ ¿©ÇàÀÚ¿¡°Ô ¿¹¹æÁ¦Á¦·Î¼ Àû´çÇÑ °ÍÀº ¾Æ´Ï´Ù.
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1. Åå¼ÒÇöóÁÁõ Ä¡·á: ÀÌ ¾àÀÇ ¿ë·®Àº ÃÖ´ë Ä¡·á È¿°ú ¹× ÃÖÀú ÀÌ»ó¹ÝÀÀ¿¡ µû¶ó Á¶½É½º·´°Ô Á¶ÀýµÇ¾î¾ß ÇÑ´Ù. ÇÊ¿äÇÑ ¿ë·®¿¡¼, ¾à¹° ³»¼ºÃø¸éÀÇ ÇöÀúÇÑ ÆíÂ÷°¡ ÀÖ´Ù. ÀþÀº ȯÀÚµéÀº °í·É ȯÀÚº¸´Ù °í¿ë·®¿¡ ³»¾à¼ºÀÌ ÀÖ´Ù. ¸ðµç ȯÀÚ¿¡°Ô Folinic acid¿ÍÀÇ º´¿ëÅõ¿©°¡ °ÇÏ°Ô ±ÇÀåµÈ´Ù.
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ÀÌ ¾àÀÇ ¼Ò¾Æ ¿ë·®Àº 1mg/kg/ÀÏÀ» 2ȸ µ¿·®À¸·Î ³ª´©¾î Åõ¿©ÇÑ´Ù; 2-4ÀÏ ÈÄ ÀÌ ¿ë·®À» ¹ÝÀ¸·Î ÁÙÀÎ ÈÄ ¾à 1´Þ°£ °è¼Ó Åõ¿©ÇÑ´Ù. ÀϹÝÀûÀÎ ¼Ò¾Æ ¼³Æù¾Æ¹Ìµå ¿ë·®À» ÀÌ ¾à°ú º´¿ëÇÏ¿© Åõ¿©ÇÑ´Ù.
2. ±Þ¼º ¸»¶ó¸®¾Æ Ä¡·á: ÀÌ ¾àÀº ±Þ¼º ¸»¶ó¸®¾Æ Ä¡·á¿¡ ´Üµ¶À¸·Î ±ÇÀåµÇÁö ¾Ê´Â´Ù. Ŭ·Î¸£Äý ¶Ç´Â Äû´Ñ°ú °°Àº ºü¸£°Ô ÀÛ¿ëÇÏ´Â schizonticides´Â ±Þ¼º ¸»¶ó¸®¾Æ Ä¡·á¿¡ »ç¿ëµÈ´Ù. ±×·¯³ª, ¼³Æù¾Æ¹Ìµå¿Í ÇÔ²² 2ÀÏ °£ ÀÌ ¾à 25mg Åõ¿©´Â ºñ-falciparum ¸»¶ó¸®¾ÆÀÇ Àü´Þ Á¶Àý ¹× ¾ïÁ¦¸¦ ½ÃÀÛÇÑ´Ù. ÀÌ ¾àÀº °¨¼ö¼º ÀÖ´Â ¸»¶ó¸®¾Æ¿øÃæ(plasmodia)°¡ Á¸ÀçÇÏ´Â Áö¿ª¿¡¼ °¨¿°µÈ ȯÀÚ¿¡°Ô¸¸ ±ÇÀåµÈ´Ù. ¸»¶ó¸®¾Æ ¹ß»ý Áö¿ª¿¡¼ ºÎºÐ¸é¿ªÈ¯ÀÚ¿¡°Ô´Â ÀÌ ¾àÀ» ´Üµ¶À¸·Î Åõ¿©ÇØ¾ß Çϸç, ±Þ¼º ¸»¶ó¸®¾Æ¿¡ ´ëÇÑ ¼ºÀÎ ¿ë·®Àº 50mgÀ» 2Àϰ£ Åõ¿©ÇÏ´Â °ÍÀÌ´Ù. 4-10¼¼ÀÇ ¼Ò¾Æ´Â 1ÀÏ 25mgÀ» 2Àϰ£ Åõ¿©ÇÏ´Â °ÍÀÌ´Ù. ¾î¶² °æ¿ìµç, ÀÓ»óÀû Ä¡·á ÈÄ ÈÇÐÀû ¿¹¹æÀ» À§ÇØ ´ÙÀ½¿¡ ³ªÅ¸³ ÁÖ 1ȸ ¿ä¹ýÀ» ÇàÇØ¾ß ÇÑ´Ù. ¾ïÁ¦¸¦ Æ÷ÇÔÇÑ ¿ä¹ýµéÀº ºü¸¥ Àç¹ß ¹× ´ÊÀº Àç¹ß ±â°£ µ¿¾È, ´Ù½Ã ¸»ÇØ °¢ °Ç¿¡¼ Àû¾îµµ 10ÁÖ µ¿¾È, È®ÀåµÇ¾î¾ß¸¸ ÇÑ´Ù.
3. ¸»¶ó¸®¾ÆÀÇ ÈÇÐÀû¿¹¹æ.
1)¼ºÀÎ ¹× 10¼¼ ÀÌ»óÀÇ ¼Ò¾Æ ȯÀÚ: 25mg(1Á¤) ÁÖ 1ȸ.
2)4-10¼¼ ¼Ò¾Æ: 12.5mg(1/2Á¤) ÁÖ 1ȸ.
3)½Å»ý¾Æ ¹× 4¼¼ ÀÌÇÏÀÇ ¼Ò¾Æ: 6.25mg(1/4Á¤) ÁÖ 1ȸ.
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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: PYRIMETHAMINEDARAPRIM (PYRIMETHAMINE)
FANSIDAR (PYRIMETHAMINE; SULFADOXINE)
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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
(pyrimethamine; )
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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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| Pharmacokinetics |
À¯·áÁ¤º¸ÀÔ´Ï´Ù.
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[º´¿ë±Ý±â ¹× ¿¬·É´ë±Ý±â ±Ù°ÅÁ¶È¸]
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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.
[»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]
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| Mechanism of Action |
Pyrimethamine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Pyrimethamine inhibits the dihydrofolate reductase of plasmodia and thereby blocks the biosynthesis of purines and pyrimidines, which are essential for DNA synthesis and cell multiplication. This leads to failure of nuclear division at the time of schizont formation in erythrocytes and liver.
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| Pharmacology |
Pyrimethamine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pyrimethamine is an antiparasitic compound commonly used as an adjunct in the treatment of uncomplicated, chloroquine resistant, P. falciparum malaria. Pyrimethamine is a folic acid antagonist and the rationale for its therapeutic action is based on the differential requirement between host and parasite for nucleic acid precursors involved in growth. This activity is highly selective against plasmodia and Toxoplasma gondii. Pyrimethamine possesses blood schizonticidal and some tissue schizonticidal activity against malaria parasites of humans. However, the 4-amino-quinoline compounds are more effective against the erythrocytic schizonts. It does not destroy gametocytes, but arrests sporogony in the mosquito. The action of pyrimethamine against Toxoplasma gondii is greatly enhanced when used in conjunction with sulfonamides.
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| Metabolism |
Pyrimethamine¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Absorption |
Pyrimethamine¿¡ ´ëÇÑ Absorption Á¤º¸ Well absorbed with peak levels occurring between 2 to 6 hours following administration
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| Pharmacokinetics |
PyrimethamineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ : Àß Èí¼öµÈ´Ù.
- ºÐÆ÷ :
- ºÐÆ÷¿ëÀû : ¼ºÀÎ : 2.9 L/kg
- À¯Áó ºÐºñ
- ´Ü¹é°áÇÕ : 80%
- ¹Ý°¨±â : 80-95 ½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 1.5-8 ½Ã°£ À̳»
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Pyrimethamine¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take with food to reduce irritation.Folic acid needs increased.
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| Drug Target |
[Drug Target]
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| Description |
Pyrimethamine¿¡ ´ëÇÑ Description Á¤º¸ One of the folic acid antagonists that is used as an antimalarial or with a sulfonamide to treat toxoplasmosis. [PubChem]
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| Dosage Form |
Pyrimethamine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Tablet Oral
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| Drug Category |
Pyrimethamine¿¡ ´ëÇÑ Drug_Category Á¤º¸ AntimalarialsAntiprotozoal AgentsAntiprotozoalsFolic Acid Antagonists
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| Smiles String Canonical |
Pyrimethamine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CCC1=C(C(N)=NC(N)=N1)C1=CC=C(Cl)C=C1
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| Smiles String Isomeric |
Pyrimethamine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CCC1=C(C(N)=NC(N)=N1)C1=CC=C(Cl)C=C1
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| InChI Identifier |
Pyrimethamine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C12H13ClN4/c1-2-9-10(11(14)17-12(15)16-9)7-3-5-8(13)6-4-7/h3-6H,2H2,1H3,(H4,14,15,16,17)/f/h14-15H2
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| Chemical IUPAC Name |
Pyrimethamine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 5-(4-chlorophenyl)-6-ethylpyrimidine-2,4-diamine
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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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