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1. ·ù¸¶Æ¼¾ç °üÀý¿°, °ñ°üÀý¿°, °Á÷¼º ôÃß¿°
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3. °ñ°Ý±ÙÀå¾Ö, ¼ö¼úÈÄ µ¿Åë, ¹ßÄ¡ÈÄ µ¿Åë, ¿ù°æ°ï¶õÁõ, °Ç¿°, Ȱ¾×³¶¿°
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1) ¼Òȼº±Ë¾ç ȯÀÚ
2) ½ÉÇÑ Ç÷¾×ÀÌ»ó ȯÀÚ
3) ½ÉÇÑ °£Àå¾Ö ȯÀÚ
4) ½ÉÇÑ ½É±â´ÉºÎÀü ȯÀÚ
5) ½ÉÇÑ ½ÅÀå¾Ö ȯÀÚ
6) ½ÉÇÑ °íÇ÷¾Ð ȯÀÚ
7) ÀÌ ¾àÀÇ ¼ººÐ ¶Ç´Â ¾Æ½ºÇǸ° µî ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¿¡ °ú¹ÎÁõÀÌ Àִ ȯÀÚ
8) ¾Æ½ºÇǸ°À̳ª ´Ù¸¥ ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦(COX-2 ÀúÇØÁ¦ Æ÷ÇÔ)¿¡ ÀÇÇÏ¿© õ½Ä, ºñ¿°, ÄÚÀÇ ¿ëÁ¾, µÎµå·¯±â, ¾Ë·¹¸£±â ¹ÝÀÀ ¶Ç´Â ±× º´·ÂÀÌ Àִ ȯÀÚ(ÀÌ·¯ÇÑ È¯ÀÚ¿¡¼ ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦ Åõ¿©ÈÄ Ä¡¸íÀûÀÎ ÁßÁõÀÇ ¾Æ³ªÇʶô½Ã¾ç ¹ÝÀÀÀÌ µå¹°°Ô º¸°íµÇ¾ú´Ù.)
9) °ü»óµ¿¸Æ ¿ìȸ·Î¼ú(CABG) ÀüÈÄ¿¡ ¹ß»ýÇÏ´Â ÅëÁõÀÇ Ä¡·á
10) ÀÌ ¾àÀº À¯´çÀ» ÇÔÀ¯Çϰí ÀÖÀ¸¹Ç·Î, °¥¶ôÅä¿À½º ºÒ³»¼º(galactose intolerance), Lapp À¯´çºÐÇØÈ¿¼Ò °áÇÌÁõ(Lapp lactase deficiency) ¶Ç´Â Æ÷µµ´ç-°¥¶ôÅä¿À½º Èí¼öÀå¾Ö(glucose-galactose malabsorption) µîÀÇ À¯ÀüÀûÀÎ ¹®Á¦°¡ Àִ ȯÀÚ¿¡°Ô´Â Åõ¿©ÇÏ¸é ¾È µÈ´Ù.
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1) ¼Òȼº±Ë¾çÀÇ º´·ÂÀÌ Àִ ȯÀÚ
2) Ç÷¾×ÀÌ»ó ¶Ç´Â ±×ÀÇ º´·ÂÀÌ Àִ ȯÀÚ
3) ÃâÇ÷°æÇâÀÌ Àִ ȯÀÚ (Ç÷¼ÒÆÇ ±â´ÉÀúÇϰ¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.)
4) °£Àå¾Ö ¶Ç´Â ±×ÀÇ º´·ÂÀÌ Àִ ȯÀÚ
5) ½ÅÀå¾Ö ¶Ç´Â ±×ÀÇ º´·ÂÀÌ Àִ ȯÀÚ ¹× ½ÅÇ÷·ù·®ÀÌ ÀúÇÏµÈ È¯ÀÚ
6) ½É±â´É Àå¾Ö ȯÀÚ
7) °íÇ÷¾Ð ȯÀÚ
8) °ú¹ÎÁõÀÇ º´·ÂÀÌ Àִ ȯÀÚ
9) ±â°üÁöõ½Ä ȯÀÚ
10) Àü½Å¼ºÈ«¹Ý¼º·çǪ½º(SLE) ȯÀÚ ¹× È¥ÇÕ°áÇÕÁ¶Á÷Áúȯ(MCTD) ȯÀÚ
11) °í·ÉÀÚ
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1) °ú¹ÎÁõ : µå¹°°Ô ¼ïÁõ»ó(È£Èí°ï¶õ, Ç÷¾Ð°ÇÏ, ¼¸Æ, ½ÄÀº¶¡, ºÎÁ¾ µî), PIEÁõÈıº(È£»ê±¸Áõ°¡¸¦ ¼ö¹ÝÇÏ´Â ÆóħÀ± : ¹ß¿, õ¸í, ±âħ, °¡·¡¸¦ µ¿¹ÝÇÔ), µÎµå·¯±â, ¶§¶§·Î ¹ßÁø, °¡·Á¿ò µîÀÇ °ú¹ÎÁõ»óÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
2) ¼Òȱâ°è : µå¹°°Ô ÅäÇ÷, À§ÀåÃâÇ÷, ¼Òȼº±Ë¾ç, õ°øÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÀÌ·¯ÇÑ °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù. ¶§¶§·Î À§ºÎºÒÄè°¨, À§Åë, º¹Åë, ±¸¿ª, ±¸Åä, ½Ä¿åºÎÁø, ¼ÒȺҷ®, °¡½¿¾²¸², ¼³»ç, º¯ºñ, ±¸³»¿° µå¹°°Ô º¹ºÎÆØ¸¸°¨, Èæº¯, ±¸°¥ µîÀÇ Áõ»óÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
3) Ç÷¾× : µå¹°°Ô ¹«°ú¸³±¸Áõ, È£»ê±¸Áõ´Ù, ¹éÇ÷±¸°¨¼Ò, Ç÷¼ÒÆÇ°¨¼Ò, Àç»ýºÒ·®¼ººóÇ÷, ¿ëÇ÷¼ººóÇ÷, Ç÷¼ÒÆÇ ±â´ÉÀúÇÏ(ÃâÇ÷½Ã°£ÀÇ ¿¬Àå) µîÀÇ Ç÷¾×Àå¾Ö°¡ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î Ç÷¾×°Ë»ç¸¦ ÇÏ´Â µî °üÂûÀ» ÃæºÐÈ÷ Çϰí ÀÌ»óÀÌ ÀÖ´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÑ´Ù.
4) °£Àå :µå¹°°Ô GOT, GPTÄ¡ÀÇ »ó½Â, Ȳ´Þ, °£¿°ÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
5) ½ÅÀå : µå¹°°Ô ½ÅÀå¾Ö, »ç±¸Ã¼ ½Å¿°, Ç÷´¢, °íÄ®·ý Ç÷Áõ, °£Áú¼º ½Å¿°, ½ÅÁõÈıº, ½ÅÀå À¯µÎ±«»ç, ´Ü¹é´¢, ½ÅºÎÀüÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
6) Á¤½Å½Å°æ°è : µå¹°°Ô ¹«±Õ¼º ¼ö¸·¿°ÀÌ º¸°íµÇ¾î ÀÖÀ¸¹Ç·Î ½ÉÇÑ µÎÅë, ±¸¿ª, ±¸Åä, ºÒ¸é, ¸ñÀÌ »»»»ÇÔ, ¹ß¿ ¶Ç´Â ÀǽÄÀå¾Ö µîÀÇ Áõ»óÀÌ ³ªÅ¸³ª¸é Áï½Ã Åõ¿©¸¦ Áß´ÜÇϰí ÀÇ»ç¿Í »óÀÇÇϸç, ƯÈ÷ ÀÚ°¡¸é¿ªÁúȯ(SLE, MCTD)ȯÀÚ¿¡°Ô´Â ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù. ¶ÇÇÑ ¶§¶§·Î Á¹À½, Àνıâ´ÉÀå¾Ö µå¹°°Ô Çö±â, µÎÅë, ¼öÁ·Àú¸², Á¤·Â°¨Åð, ÇÇ·Î, ¿ì¿ï, ºñÁ¤»óÀûÀÎ ²Þ, ÁýÁß´É·Â »ó½Ç, Áö³²·Â »ó½Ç, ºÒ¸é, ±ÙÀ°Åë, ±Ù¼è¾àÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
7) ÇǺΠ: ¶§¶§·Î ½ÀÁø, ¹ßÇÑ(¶¡ÀÌ ³²), ÀÚ¹Ý(ÀÚÁÖ»ö ¹ÝÁ¡) µå¹°°Ô ±¤°ú¹ÎÁõ, Å»¸ð, ¹ßÀû(ÃæÇ÷µÇ¾î ºÓ¾îÁü), ±«»ç¼º¿ëÇØ, ´ÙÇü¼ºÈ«¹Ý(¿©·¯ ¸ð¾çÀÇ ºÓÀº ¹ÝÁ¡), ½ºÆ¼ºì½º-Á¸½¼ÁõÈıº(ÇǺÎÁ¡¸·¾ÈÁõÈıº), µÎµå·¯±â, Ç¥ÇÇ ¼öÆ÷ÁõÀÌ ³ªÅ¸³ª°Å³ª È£»ê±¸ Áõ°¡ ¹× Àü½Å Áõ»ó µ¿¹Ý ¾à¹° ¹ÝÀÀ, °íÁ¤¾à¹°¹ßÁøÀÌ ³ªÅ¸³¯ ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇϰí ÀÌ»óÀÌ ÀÖ´Â °æ¿ì¿¡´Â Åõ¿©¸¦ ÁßÁöÇÏ´Â µî ÀûÀýÇÑ Á¶Ä¡¸¦ ÇÑ´Ù.
8) °¨°¢±â°è : À̸í, û°¢Àå¾Ö, ½Ã°¢Àå¾Ö°¡ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
9) ±âŸ : ¶§¶§·Î ºÎÁ¾, È£Èí°ï¶õ, µå¹°°Ô ½É°èÇ×Áø, ±Ù¹«·ÂÁõ, ¿ïÇ÷¼º½ÉºÎÀü, È£»ê±¸¼º Æó·Å, ¾Æ³ªÇʶô½Ã¾ç ¹ÝÀÀ, ¿ù°æÀå¾Ö, ¿ÀÇѰú ¹ß¿, ¸Æ°ü¿°, °íÇ÷´ç, ÀúÇ÷´çÀÌ ³ªÅ¸³¯ ¼ö ÀÖ´Ù.
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1) ´Ù¸¥ ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦(NSAIDs) ¹× ³ªÇÁ·Ï¼¾ À¯µµÃ¼¿Í º´¿ëÇÒ °æ¿ì ÀÌ»ó¹ÝÀÀÀÇ À§ÇèÀÌ Áõ°¡ÇÒ ¼ö ÀÖÀ¸¹Ç·Î º´¿ëÇÏÁö ¾Ê´Â´Ù.
2) È÷´ÜÅäÀΰè Ç×°£ÁúÁ¦, ¼³ÆÄÁ¦, ¼³Æ÷´Ò¿ä¼Ò°è Ç÷´ç°ÇÏÁ¦: ÀÌ·¯ÇÑ ¾à¹°°ú º´¿ëÅõ¿©½Ã ±× ÀÛ¿ëÀ» Áõ°½Ãų ¼ö ÀÖÀ¸¹Ç·Î ÃæºÐÈ÷ °üÂûÇÏ°í ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
3) ÇÁ·ÎÇÁ¶ó³î·Ñ ¹× ´Ù¸¥ ¥â-Â÷´ÜÁ¦: ÀÌ ¾à°úÀÇ º´¿ëÅõ¿©·Î ÀÎÇØ Ç×°íÇ÷¾Ð È¿°ú°¡ °¨¼ÒµÉ ¼ö ÀÖ´Ù.
4) ACE ÀúÇØÁ¦(İÅäÇÁ¸± µî)
¨ç ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¿¡ ÀÇÇØ ACE ÀúÇØÁ¦ÀÇ Ç×°íÇ÷¾ÐÈ¿°ú°¡ °¨¼ÒµÉ ¼ö ÀÖ´Ù´Â º¸°í°¡ ÀÖÀ¸¹Ç·Î ÀÌ ¾à°ú ACE ÀúÇØÁ¦¸¦ º´¿ëÅõ¿©ÇÏ´Â °æ¿ì ÀÌ·¯ÇÑ »óÈ£ÀÛ¿ëÀ» ¿°µÎ¿¡ µÎ¾î¾ß ÇÑ´Ù.
¨è ACEÀúÇØÁ¦(İÅäÇÁ¸±)¿ÍÀÇ º´¿ë¿¡ ÀÇÇØ, ½ÅÀå¾Ö¸¦ ÀÏÀ¸Å³ ¼ö ÀÖÀ¸¹Ç·Î, º´¿ëÇÏ´Â °æ¿ì¿¡´Â ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
5) ·çÇÁ°è ÀÌ´¢Á¦ ¹× Ä¡¾ÆÁþ°è ÀÌ´¢Á¦
¨ç ÀÓ»ó½ÃÇè ¹× ½ÃÆÇÈÄ Á¶»ç °á°ú ÀÌ ¾àÀÇ ½ÅÀå¿¡¼ÀÇ ÇÁ·Î½ºÅ¸±Û¶õµò ÇÕ¼º ¾ïÁ¦¿¡ ÀÇÇØ ÀϺΠȯÀÚ¿¡¼ Ǫ·Î¼¼¹Ìµå ¹× Ä¡¾ÆÁþ°è ÀÌ´¢Á¦ÀÇ ³ªÆ®·ý´¢¹è¼³ È¿°ú°¡ °¨¼ÒÇÒ ¼ö ÀÖÀ½ÀÌ È®ÀεǾú´Ù. ÀÌµé ¾à¹°°ú ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¸¦ º´¿ëÅõ¿©ÇÏ´Â µ¿¾È ½ÅºÎÀü ¡Èĸ¦ ¸é¹ÐÈ÷ °üÂûÇØ¾ß ÇÑ´Ù.
¨è ÀÌ ¾àÀº ·çÇÁ°è ÀÌ´¢Á¦(Ǫ·Î¼¼¹Ìµå, ÇÇ·¹Å¸´Ïµå) ¹× Ä¡¾ÆÁþ°è ÀÌ´¢Á¦ÀÇ ÀÛ¿ëÀ» °¨¼Ò½Ãų ¼ö ÀÖÀ¸¹Ç·Î º´¿ëÅõ¿©ÇÏ´Â °æ¿ì¿¡´Â ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
6) ÇÁ·Îº£³×½Ãµå: º´¿ëÅõ¿©½Ã ÀÌ ¾àÀÇ Ç÷Áß³óµµ°¡ »ó½ÂÇÏ¿© Ç÷Áß ¹Ý°¨±â°¡ ¿¬ÀåµÇ¹Ç·Î °¨·®ÇÏ´Â µî ½ÅÁßÈ÷ Åõ¿©ÇÑ´Ù.
7) ¾Æ½ºÇǸ° : ¾Æ½ºÇǸ°°úÀÇ º´¿ëÀÌ ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦ÀÇ »ç¿ë°ú °ü·ÃµÈ Áß´ëÇÑ ½ÉÇ÷°ü°è Ç÷Àü¹ÝÀÀÀÇ À§ÇèÀ» °¨¼Ò½Ãų ¼ö ÀÖ´Ù´Â ÀϰüµÈ Áõ°Å´Â ¾ø´Ù. ´Ù¸¥ ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¿Í ¸¶Âù°¡Áö·Î ÀÌ ¾à°ú ¾Æ½ºÇǸ°ÀÇ º´¿ë¿¡ ÀÇÇØ ÁßÁõÀÇ À§Àå°ü°è ÀÌ»ó¹ÝÀÀÀÇ ¹ß»ý À§ÇèÀÌ Áõ°¡µÉ ¼ö ÀÖÀ¸¹Ç·Î µÎ ¾à¹°ÀÇ º´¿ëÀº ÀϹÝÀûÀ¸·Î ±ÇÀåµÇÁö ¾Ê´Â´Ù. ÀÓ»ó ¾àµ¿ÇÐÀû µ¥ÀÌÅÍ¿¡ µû¶ó, ÀÌÆ² ÀÌ»ó ¿¬¼ÓÇÏ¿© º´¿ëÇÒ °æ¿ì Àú¿ë·®ÀÇ ¾Æ½ºÇǸ°ÀÌ Ç÷¼ÒÆÇ Ȱµ¿¿¡ ¹ÌÄ¡´Â ¿µÇâÀ» ¾ïÁ¦ÇÒ ¼ö ÀÖ°í, ÀÌ·¯ÇÑ ¾ïÁ¦´Â µ¿ ¼ººÐ Ä¡·á Áß´Ü ÀÌÈÄ ÃÖ´ë ¸çÄ¥°£ Áö¼ÓµÉ ¼ö ÀÖ´Ù. ÀÌ·¯ÇÑ »óÈ£ÀÛ¿ëÀÇ ÀÓ»óÀû °ü·Ã¼ºÀº ¾Ë·ÁÁ® ÀÖÁö ¾Ê´Ù.
8) ¸®Æ¬ : ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦´Â ½ÅÀå¿¡¼ÀÇ ÇÁ·Î½ºÅ¸±Û¶õµò ÇÕ¼º ¾ïÁ¦¿¡ ÀÇÇØ Ç÷û ¸®Æ¬ÀÇ ³óµµ¸¦ Áõ°¡½ÃŰ°í ¸®Æ¬ÀÇ ½ÅŬ¸®¾î·±½º¸¦ °¨¼Ò½Ãų ¼ö ÀÖ´Ù. ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦¿Í ¸®Æ¬ÀÇ º´¿ë Åõ¿© ½Ã ¸®Æ¬Áßµ¶À» ÀÏÀ¸Å³ ¼ö ÀÖÀ¸¹Ç·Î, º´¿ëÇÏ´Â °æ¿ì ¸®Æ¬ÀÇ µ¶¼ºÂ¡Èĸ¦ ÁÖÀDZí°Ô °üÂûÇÏ°í °¨·®ÇÏ´Â µî ½ÅÁßÈ÷ Åõ¿©ÇØ¾ß ÇÑ´Ù.
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| Mechanism of Action |
Naproxen¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ The mechanism of action of naproxen, like that of other NSAIDs, is believed to be associated with the inhibition of cyclooxygenase activity. Two unique cyclooxygenases have been described in mammals. The constitutive cyclooxygenase, COX-1, synthesizes prostaglandins necessary for normal gastrointestinal and renal function. The inducible cyclooxygenase, COX-2, generates prostaglandins involved in inflammation. Inhibition of COX-1 is thought to be associated with gastrointestinal and renal toxicity while inhibition of COX-2 provides anti-inflammatory activity.
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| Pharmacology |
Naproxen¿¡ ´ëÇÑ Pharmacology Á¤º¸ Naproxen is a member of the arylacetic acid group of nonsteroidal anti-inflammatory drugs (NSAIDs). Naproxen has analgesic and antipyretic properties. As with other NSAIDs, its mode of action is not fully understood; however, its ability to inhibit prostaglandin synthesis may be involved in the anti-inflammatory effect.
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| Metabolism |
Naproxen¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Not Available
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| Protein Binding |
Naproxen¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ At therapeutic levels naproxen is greater than 99% albumin-bound.
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| Half-life |
Naproxen¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ The observed terminal elimination half-life is approximately 15 hours.
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| Absorption |
Naproxen¿¡ ´ëÇÑ Absorption Á¤º¸ Naproxen itself is rapidly and completely absorbed from the GI tract with an in vivo bioavailability of 95%. Although naproxen itself is well absorbed, the sodium salt form is more rapidly absorbed resulting in higher peak plasma levels for a given dose. Food causes a slight decrease in the rate absorption.
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| Pharmacokinetics |
Naproxen sodiumÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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| Biotransformation |
Naproxen¿¡ ´ëÇÑ Biotransformation Á¤º¸ Naproxen is extensively metabolized to 6-0-desmethyl naproxen and both parent and metabolites do not induce metabolizing enzymes.
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| Toxicity |
Naproxen¿¡ ´ëÇÑ Toxicity Á¤º¸ ORAL (LD50): Acute: 248 mg/kg [Rat]. 360 mg/kg [Mouse]. Symptoms of overdose include drowsiness, heartburn, indigestion, nausea, and vomiting.
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| Drug Interactions |
Naproxen¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Alendronate Increased risk of gastric toxicityMethotrexate The NSAID increases the effect and toxicity of methotrexateAnisindione The NSAID increases the anticoagulant effectDicumarol The NSAID increases the anticoagulant effectAcenocoumarol The NSAID increases the anticoagulant effectWarfarin The NSAID increases the anticoagulant effectLithium The NSAID increases serum levels of lithiumCyclosporine Monitor for nephrotoxicity
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸] Naproxen¿¡ ´ëÇÑ P450 table
SUBSTRATES
CYP 1A2
clozapine
cyclobenzaprine
imipramine
mexiletine
**naproxen**
riluzole
tacrine
theophylline
INHIBITORS
CYP 1A2
cimetidine
fluoroquinolones
fluvoxamine
ticlopidine
INDUCERS
CYP 1A2
tobacco
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| Food Interaction |
Naproxen¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take with food.Take with a full glass of water.
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| Drug Target |
[Drug Target]
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| Description |
Naproxen¿¡ ´ëÇÑ Description Á¤º¸ An anti-inflammatory agent with analgesic and antipyretic properties. Both the acid and its sodium salt are used in the treatment of rheumatoid arthritis and other rheumatic or musculoskeletal disorders, dysmenorrhea, and acute gout. [PubChem]
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| Drug Category |
Naproxen¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Inflammatory Agents, Non-SteroidalCyclooxygenase InhibitorsGout Suppressants
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| Smiles String Canonical |
Naproxen¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ COC1=CC2=C(C=C1)C=C(C=C2)C(C)C(O)=O
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| Smiles String Isomeric |
Naproxen¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ COC1=CC2=C(C=C1)C=C(C=C2)[C@@H](C)C(O)=O
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| InChI Identifier |
Naproxen¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C14H14O3/c1-9(14(15)16)10-3-4-12-8-13(17-2)6-5-11(12)7-10/h3-9H,1-2H3,(H,15,16)/f/h15H
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| Chemical IUPAC Name |
Naproxen¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2-(6-methoxynaphthalen-2-yl)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.
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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