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1) ÀÌ ¾à¿¡ °ú¹ÎÁõ ȯÀÚ
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2) È£Èí±â°è : È£ÈíÁ¤Áö, ÈäÅë, È£Èí°ï¶õÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
3) ÇǺΠ: ¹ßÁø, °¡·Á¿ò, µÎµå·¯±â, ±¤°ú¹ÎÁõÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
4) ¼Òȱâ°è : ±¸¿ª, ±¸Åä, º¹Åë, ¼³»ç, ½Ä¿åºÎÁø, ±¸°°ÇÁ¶, ½ÊÀÌÁöÀå±Ë¾ç, À§Àå°üÃâÇ÷, ¼è¾àȯÀÚ¿¡ Â×¾î Ä¡¸íÀûÀÎ °á°ú¸¦ ÃÊ·¡ÇÒ ¼ö ÀÖ´Â ±Þ¼º°£¼Õ»ó, °£±â´ÉÀå¾Ö, Ȳ´Þ, ±Ë¾ç¼º´ëÀå¿°, ºô¸®·çºóÄ¡ »ó½ÂÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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7) ½Å°æ°è : ¿îµ¿½ÇÁ¶, û°¢»ó½Ç, µÎÅë, Áö°¢ÀÌ»ó, ÆÄŲ½¼º´, ¸»ÃʽŰæÁõ, ¹ß¿, Çö±âÁõ, ÁøÁ¤, °æ·ÃÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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1) Ç×Á¾¾çÁ¦ÀÎ cytosine arabinosideÀÇ °æÀïÀû ¾ïÁ¦·Î ÀÎÇØ ÀÌ ¾àÀÇ Ç×Áø±ÕÀÛ¿ëÀ» ºÒȰ¼ºÈ½ÃŲ´Ù´Â °ÍÀÌ º¸°íµÇ¾ú´Ù.
2) »ç±¸Ã¼ ¿©°ú¸¦ ¼Õ»ó½ÃŰ´Â Á¦Á¦µéÀº FlucytosineÀÇ »ý¹°ÇÐÀû ¹Ý°¨±â¸¦ ¿¬Àå½Ãų ¼ö ÀÖ´Ù.
3) ÀÌ ¾à°ú Polyene°è Ç×»ýÁ¦, ƯÈ÷ ¾ÏÆ÷Å׸®½Å B¿ÍÀÇ Ç×Áø±ÕÀû »ó½ÂÀÛ¿ëÀÌ º¸°íµÇ¾ú´Ù.
4) ¹æ»ç¼±Ä¡·á ¹× °ñ¼ö¾ïÁ¦¸¦ ÀÏÀ¸Å°´Â ¾à¹°À» Åõ¿©ÇÏ´Â °æ¿ì¿¡´Â °ñ¼ö±â´É¾ïÁ¦ÀÛ¿ëÀ» Áõ°½Ãų ¼ö ÀÖ´Ù.
5) Å×°¡Çª¸£?±â¿¡½ºÅ¹Æ®?¿À¸Þ½ºÅ¹Æ®Ä®·ý ¹èÇÕÁ¦¿Í º´¿ëÅõ¿©½Ã Á¶±â¿¡ ½É°¢ÇÑ Ç÷¾×Àå¾Ö ¹× ¼³»ç, ±¸³»¿° µîÀÇ ¼ÒȰüÀå¾Ö µîÀÌ ±Ý¹æ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î Å×°¡Çª¸£?±â¿¡½ºÅ¹Æ®?¿À¸Þ½ºÅ¹Æ®Ä®·ý ¹èÇÕÁ¦ Åõ¿©Áß ¹× Åõ¿©ÁßÁöÈÄ Àû¾îµµ 7ÀÏ À̳»¿¡´Â ÀÌ ¾àÀ» Åõ¿©ÇÏÁö ¸» °Í.
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| Related FDA Approved Drug |
±âÁØ ¼ººÐ: FLUCYTOSINEANCOBON (FLUCYTOSINE)
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µå·°ÀÎÆ÷ ÀǾàǰ ¿ä¾à/»ó¼¼Á¤º¸
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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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½ÅÀå¾Ö, °£Àå¾Ö½Ã ¿ë·®Á¶Àý |
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º¹¾àÀ̹ÌÁö´Â ¸ðµç º¹¾àÁöµµ »çÇ×À» Ç¥½ÃÇѰÍÀº ¾Æ´Ï¸ç, Ãß°¡ÀûÀ¸·Î ¾÷µ¥ÀÌÆ®µÇ°Å³ª ¼öÁ¤µÉ ¼ö ÀÖ½À´Ï´Ù. |
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º¹¾àÀ̹ÌÁöÀÇ Ç¥½Ã¿©ºÎ´Â ½ÇÁ¦ ¾à¹°º¹¿ë½Ã Á߿䵵¿¡ µû¸¥°ÍÀº ¾Æ´Ï¸ç ´Ü¼øÈ÷ Çã°¡Á¤º¸»ó Ű¿öµå¸¦ ±âÁØÀ¸·Î µî·ÏµÇ¾ú½À´Ï´Ù. |
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±ÍÇϰ¡ º¹¾àÀ̹ÌÁö Á¤º¸¸¦ ½Å·ÚÇÔÀº ÀüÀûÀ¸·Î ±ÍÇÏÀÇ Ã¥ÀÓÀÔ´Ï´Ù. µå·°ÀÎÆ÷´Â ÀÌ¿¡ ´ëÇÑ ¾î¶°ÇÑ º¸Áõµµ ÇÏÁö ¾Ê½À´Ï´Ù. |
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°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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| Mechanism of Action |
Flucytosine¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Although the exact mode of action is unknown, it has been proposed that flucytosine acts directly on fungal organisms by competitive inhibition of purine and pyrimidine uptake and indirectly by intracellular metabolism to 5-fluorouracil. Flucytosine enters the fungal cell via cytosine permease; thus, flucytosine is metabolized to 5-fluorouracil within fungal organisms. The 5-fluorouracil is extensively incorporated into fungal RNA and inhibits synthesis of both DNA and RNA. The result is unbalanced growth and death of the fungal organism. It also appears to be an inhibitor of fungal thymidylate synthase.
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| Pharmacology |
Flucytosine¿¡ ´ëÇÑ Pharmacology Á¤º¸ Flucytosine is an antimetabolite that acts as an antifungal agent with in vitro and in vivo activity against Candida and Cryptococcus. Flucytosine enters the fungal cell via cytosine permease; thus, flucytosine is metabolized to 5-fluorouracil within fungal organisms. The 5-fluorouracil is extensively incorporated into fungal RNA and inhibits synthesis of both DNA and RNA. The result is unbalanced growth and death of the fungal organism. Antifungal synergism between Ancobon and polyene antibiotics, particularly amphotericin B, has been reported.
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| Absorption |
Flucytosine¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly and virtually completely absorbed following oral administration. Bioavailability 78% to 89%.
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| Pharmacokinetics |
FlucytosineÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- »ýü³»ÀÌ¿ë·ü : °æ±¸ : 75-90%
- ºÐÆ÷ : ÁßÃ߽Űæ°è¿Í ±â°üÁö ºÐºñ¹°¿¡ ºÐÆ÷ÇÑ´Ù.
- ´Ü¹é°áÇÕ : 2-4%
- ´ë»ç : °ÅÀÇ ´ë»çµÇÁö ¾Ê´Â´Ù.
- ¹Ý°¨±â :
- Á¤»ó ¼ºÀÎ : 3-8 ½Ã°£
- ¹«´¢Áõ : 200½Ã°£ ±îÁö Áõ°¡µÉ ¼ö ÀÖ´Ù.
- ¸»±â ½ÅÁúȯ : 75-200 ½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : 2-6 ½Ã°£ À̳»
- ¼Ò½Ç : 75-90%°¡ »ç±¸Ã¼¿©°ú¸¦ ÅëÇØ ¹Ìº¯Èü·Î ½Å¹è¼³
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| Toxicity |
Flucytosine¿¡ ´ëÇÑ Toxicity Á¤º¸ Oral, rat: LD50 = >15 gm/kg.
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| Drug Interactions |
Flucytosine¿¡ ´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 |
Flucytosine¿¡ ´ëÇÑ Description Á¤º¸ A fluorinated cytosine analog that is used as an antifungal agent. [PubChem]
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| Dosage Form |
Flucytosine¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralSolution Intravenous
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| Drug Category |
Flucytosine¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antifungal AgentsAntifungalsAntimetabolites
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| Smiles String Canonical |
Flucytosine¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC1=C(F)C=NC(=O)N1
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| Smiles String Isomeric |
Flucytosine¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ NC1=C(F)C=NC(=O)N1
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| InChI Identifier |
Flucytosine¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C4H4FN3O/c5-2-1-7-4(9)8-3(2)6/h1H,(H3,6,7,8,9)/f/h8H,6H2
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| Chemical IUPAC Name |
Flucytosine¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 4-amino-5-fluoro-3H-pyrimidin-2-one
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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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