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Àν¶¸° Á¦Á¦, ºñÄí¾Æ´Ïµå°è ¾àÁ¦, ¾ËÆÄ-±Û·çÄڽôÙÁ¦ ÀúÇØÁ¦(¾ÆÄ«¸£º¸½º), ÇǶóÁ¹·Ð°è ¼Ò¿°Á¦(Æä´ÒºÎŸÁ¸ µî), ÇÁ·Îº£³×½Ãµå, Äí¸¶¸°°è ¾àÁ¦, »ì¸®½Ç»êÁ¦(¾Æ½ºÇǸ° µî), ¥â-Â÷´ÜÁ¦(ÇÁ·ÎÇÁ¶ó³ë·Ñ), MAO ÀúÇØÁ¦, ¼³ÆÄÁ¦, µðÈ÷µå·Î¿¡¸£°íŸ¹Î Á¦Á¦, Ŭ·Î¶÷Æä´ÏÄÝ, Åׯ®¶ó»çÀÌŬ¸°°è Ç×»ý¹°Áú, Ŭ·ÎÇǺ극ÀÌÆ®
2) °¨¾àÇÏ´Â ¾àÁ¦
¿¡Çdz×ÇÁ¸°, ºÎ½ÅÇÇÁúÈ£¸£¸ó, °©»ó¼±È£¸£¸ó, ³Æ÷È£¸£¸ó, ÀÌ´¢Á¦, ÇǶóÁø¾Æ¹Ìµå, À̼ҴϾÆÁöµå, ´ÏÄÚÆ¾»ê, Æä³ëÄ¡¾ÆÁø°è ¾àÁ¦
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1) ´ÙÀ½ ¾àÁ¦¿Í º´¿ë¿¡ ÀÇÇØ À¯»ê»êÁõÀÌ ÀϾ ¼ö ÀÖÀ¸¹Ç·Î À̰Ͱú º´¿ëÇÒ °æ¿ì¿¡´Â ȯÀÚÀÇ »óŸ¦ ÃæºÐÈ÷ °üÂûÇϰí Åõ¿©ÇÒ °Í : ¿ä¿ÀµåÁ¶ÇüÁ¦, ½Åµ¶¼ºÀÌ °ÇÑ Ç×»ý¹°Áú(°ÕŸ¸¶À̽еî)
2) ´ÙÀ½ ¾àÁ¦¿Í º´¿ë¿¡ ÀÇÇØ Ç÷´ç°ÇÏ ÀÛ¿ëÀÌ Áõ° ¶Ç´Â °¨¾àµÇ´Â °ÍÀÌ ÀÖÀ¸¹Ç·Î º´¿ëÇÏ´Â °æ¿ì¿¡´Â Ç÷´çÄ¡ ¹× ´Ù¸¥ ȯÀÚÀÇ »óŸ¦ ÃæºÐÈ÷ °üÂûÇÏ¸é¼ Åõ¿©ÇÑ´Ù.
¨ç Áõ°ÇÏ´Â ¾àÁ¦
Àν¶¸°Á¦Á¦, ¼³Æ÷´Ò¾Æ¹Ìµå°è ¹× ¼³Æ÷´Ò¿ì·¹¾Æ°è ¾àÁ¦, ¾ËÆÄ-±Û¸®ÄڽôÙÁ¦ ÀúÇØÁ¦(¾ËÄ®·ÎÆ÷½º), ´Ü¹éµ¿È½ºÅ×·ÎÀ̵å, ±¸¾Æ³×Ƽµò, »ì¸®½Ç»êÁ¦(¾Æ½ºÇǸ° µî), ¥â-Â÷´ÜÁ¦(ÇÁ·ÎÇÁ¶ó³î·Ñ µî), ¸ð³ë¾Æ¹Î»êÈ È¿¼ÒÀúÇØÁ¦
¨è °¨¾àÇÏ´Â ¾àÁ¦
¿¡Çdz×ÇÁ¸°, ºÎ½ÅÇÇÁúÈ£¸£¸ó, °©»ó¼±È£¸£¸ó, ³Æ÷È£¸£¸ó, ÀÌ´¢Á¦, ÇǶóÁø¾Æ¹Ìµå, À̼ҴϾÆÁöµå, ´ÏÄÚÆ¾»ê, Æä³ëÄ¡¾ÆÁø°è ¾àÁ¦
3) ±Û¸®ºÎ¶óÀ̵å : Àν¶¸° ºñÀÇÁ¸¼º ´ç´¢º´ÀΠȯÀÚ¿¡¼ ´Üȸ Åõ¿©·Î º»Á¦¿Í ±Û¸®ºÎ¶óÀ̵åÀÇ º´¿ë Åõ¿©´Â º»Á¦ÀÇ ¾à¹° µ¿·ÂÇÐÀû ȤÀº ¾à¹° µ¿ÅÂÇÐÀû ¼ºÁú¿¡ º¯È¸¦ ÀÏÀ¸Å°Áö ¾Ê´Â´Ù. ±Û¸®ºÎ¶óÀ̵åÀÇ AUC¿Í Cmax°¡ °¨¼ÒÇÏ´Â °ÍÀÌ °üÂûµÇ¾úÀ¸³ª, ÆíÂ÷°¡ Å©´Ù. ÀÌ ¿¬±¸¿¡¼ ´Üȸ Åõ¿©ÀÇ ¼º°Ý°ú º»Á¦ÀÇ Ç÷¾×³óµµ¿Í ¾à¹° µ¿ÅÂÇÐÀû È¿°ú°£ÀÇ »ó°ü °ü°è°¡ ¾ø´Â °ÍÀº ÀÌ·± »óÈ£ ÀÛ¿ëÀÇ ÀÓ»óÀû À¯ÀǼºÀÌ ºÒ¸íÈ®ÇÏ´Ù´Â °ÍÀ» ³ªÅ¸³½´Ù.
4) Ǫ·Î¼¼¹Ìµå : °Ç°ÇÑ »ç¶÷¿¡¼ ´Üȸ Åõ¿©·Î º»Á¦-Ǫ·Î¼¼¹ÌµåÀÇ ¾à¹°»óÈ£ÀÛ¿ë¿¡ ´ëÇÑ ¿¬±¸´Â, º´¿ëÅõ¿©¿¡ ÀÇÇØ °¢ ¹°ÁúÀÇ ¾à¹°µ¿·ÂÇÐÀû ¼öÄ¡µéÀÌ ¿µÇâÀ» ¹Þ´Â´Ù´Â °ÍÀ» ³ªÅ¸³½´Ù. Ǫ·Î¼¼¹Ìµå´Â º»Á¦ÀÇ ½ÅÀå û¼ÒÀ²ÀÇ À¯ÀÇÀûÀÎ º¯È¾øÀÌ º»Á¦ÀÇ Ç÷Àå³óµµ¸¦ Áõ°¡½Ã۸ç, Ç÷Áß Cmax¸¦ 22%, Ç÷Áß AUC¸¦ 15% Áõ°¡½ÃŲ´Ù. º»Á¦¿Í ÇÔ²² Åõ¿©ÇßÀ» ¶§, ´ÜÀÏÅõ¿©¿¡ ºñÇØ Ǫ·Î¼¼¹ÌµåÀÇ Cmax¿Í AUC°¡ °¢°¢ 31%¿Í 12% °¨¼ÒµÇ¾úÀ¸¸ç, Ǫ·Î¼¼¹ÌµåÀÇ ½ÅÀå û¼ÒÀ²ÀÇ º¯È ¾øÀÌ ÃÖÁ¾¹Ý°¨±â¸¦ 32% °¨¼Ò½ÃŲ´Ù. ¸¸¼ºÀûÀ¸·Î º»Á¦¿Í Ǫ·Î¼¼¹Ìµå¸¦ º´¿ëÅõ¿©½Ã »óÈ£ÀÛ¿ë¿¡ °üÇÑ À¯¿ëÇÑ Á¤º¸´Â ¾ø´Ù.
5) ´ÏÆäµðÇÉ : Á¤»óÀÎ °Ç°ÇÑ Áö¿øÀÚ¿¡¼ ´ÜȸÅõ¿©·Î º»Á¦-´ÏÆäµðÇÉÀÇ ¾à¹°»óÈ£ÀÛ¿ë¿¡ ´ëÇÑ ¿¬±¸´Â ´ÏÆäµðÇɰúÀÇ º´¿ëÅõ¿©°¡ Ç÷Àå º»Á¦ÀÇ Cmax¿Í AUC¸¦ °¢°¢ 20%¿Í 9% Áõ°¡½Ã۸ç, ´¢Áß ¹è¼³À» Áõ°¡½ÃŲ´Ù. Tmax¿Í ¹Ý°¨±â´Â ¿µÇâÀÌ ¾ø´Ù. ´ÏÆäµðÇÉÀº º»Á¦ÀÇ Èí¼ö¸¦ ÃËÁø½ÃŲ´Ù. º»Á¦´Â ´ÏÆäµðÇÉ¿¡ ÃÖ¼ÒÇÑÀÇ È¿°ú¸¦ ³ªÅ¸³½´Ù.
6) ½Å±â´É¿¡ ¿µÇâÀ» ¹ÌÄ¥ ¼ö Àְųª À¯ÀÇÇÑ Ç÷¿ªÇÐÀû º¯È¸¦ ¾ß±âÇϰųª ½Å¼¼´¢°ü ºÐºñ·Î¼ ¹è¼³µÇ´Â ¾çÀ̿ ¾à¹°°ú °°ÀÌ ÀÌ ¾à¿¡ ¿µÇâÀ» ¹ÌÄ¥ ¼ö ÀÖ´Â ¾à¹° : ¸ÞÆ®Æ÷¸£¹ÎÀºÀ¯±â¾çÀ̿¼ö¼Ûü(Organic Cation transporter, OCT) OCT1, OCT2ÀÇ ±âÁúÀÌ´Ù.
- OCT1 ¾ïÁ¦Á¦(º£¶óÆÄ¹Ð µî)¿Í º´¿ë ½Ã ¸ÞÆ®Æ÷¸£¹ÎÀÇ ¾àÈ¿°¡ ÀúÇϵɼö ÀÖÀ½
- OCT1 À¯µµÁ¦(¸®ÆÊÇǽеî)¿Í º´¿ë ½Ã ¸ÞÆ®Æ÷¸£¹ÎÀÇ À§Àå°ü Èí¼ö ¹×¾àÈ¿°¡ Áõ°¡µÉ ¼ö ÀÖÀ½
- OCT2 ¾ïÁ¦Á¦(½Ã¸ÞƼµò, µ¹·çÅ×±×¶óºñ¸£, ¶ó³î¶óÁø, Æ®¸®¸ÞÅäÇÁ¸², ¹Ýµ¥Å¸´Õ, ÀÌ»çºÎÄÚ³ªÁ¹ µî)¿Í º´¿ë ½Ã ¸ÞÆ®Æ÷¸£¹ÎÀÇ ½Å¹è¼³À» °¨¼Ò½Ãų¼ö ÀÖ¾î ¸ÞÆ®Æ÷¸£¹ÎÀÇ Ç÷Áß ³óµµ°¡ »ó½ÂÇÒ ¼ö ÀÖÀ½
- OCT2, OCT1 µ¿½Ã ¾ïÁ¦Á¦(Å©¸®Á¶Æ¼´Õ, ¿Ã¶óÆÄ¸³)¿Í º´¿ë ½Ã ¸ÞÆ®Æ÷¸£ ¹ÎÀÇ ½Å¹è¼³ ¹× ¾àÈ¿¿¡ ¿µÇâÀ» ÁÙ ¼ö ÀÖÀ½
µû¶ó¼ ¸ÞÆ®Æ÷¸£¹Î°ú ÀÌ·¯ÇÑ ¾à¹°À» º´¿ë Åõ¿© ÇÒ °æ¿ì ¸ÞÆ®Æ÷¸£¹ÎÀÇ Ç÷Áß ³óµµ°¡ »ó½ÂÇÒ ¼ö ÀÖÀ¸¹Ç·Î, ÀÌ Á¡¿¡ ´ëÇÏ¿© ƯÈ÷ ½ÅÀå¾Ö ȯÀÚÀÇ °æ¿ì ÁÖÀǰ¡ ÇÊ¿äÇÏ´Ù. OCT ¾ïÁ¦Á¦/À¯µµÁ¦´Â ¸ÞÆ®Æ÷¸£¹ÎÀÇ ¾àÈ¿¸¦ º¯È½Ãų ¼ö ÀÖÀ¸¹Ç·Î ÇÊ¿äÇÑ °æ¿ì ¸ÞÆ®Æ÷¸£¹ÎÀÇ ¿ë·® Á¶ÀýÀ» °í·ÁÇÒ ¼öÀÖ´Ù.
¶ÇÇÑ, ¼±ÅÃÀû COX-II(Cyclo-oxygenase) ¾ïÁ¦Á¦¸¦ Æ÷ÇÔÇÑ ºñ½ºÅ×·ÎÀ̵强 ¼Ò¿°ÁøÅëÁ¦(NSAIDs), ¾ÈÁö¿ÀÅÙ½ÅÀüȯȿ¼Ò ¾ïÁ¦Á¦(ACE inhibitors), ¾ÈÁö¿ÀÅٽŠII ¼ö¿ëü ±æÇ×Á¦(angiotensin II receptor antagonists), ÀÌ´¢ Á¦(ƯÈ÷ ·çÇÁ ÀÌ´¢Á¦) µîÀº ½Å±â´É¿¡ ºÒ¸®ÇÑ ¿µÇâÀ» ÁÙ ¼ö ÀÖ¾î À¯»ê »êÁõÀÇ À§ÇèÀ» Áõ°¡½Ãų ¼ö ÀÖÀ¸¹Ç·Î, ¸ÞÆ®Æ÷¸£¹Î°ú º´¿ë Åõ¿© ÇÒ °æ¿ì ½Å±â´ÉÀ» ¸é¹ÐÇÏ°Ô °üÂûÇØ¾ß ÇÑ´Ù.
7) ±âŸ : °íÇ÷´çÀ» À¯¹ßÇÏ´Â °æÇâÀÌ ÀÖ´Â ¾à¹°Àº Ç÷´çÁ¶ÀýÀ» ÀÒ°Ô ÇÒ ¼ö ÀÖ´Ù. ÀÌ·¯ÇÑ ¾à¹°Àº ´ÙÀ̾ÆÁöµå¿Í ´Ù¸¥ ÀÌ´¢Á¦, ÄÚÆ¼ÄÚ½ºÅ×·ÎÀ̵å, Æä³ë´ÙÀ̾ÆÁø, °©»ó¼±È£¸£¸óÁ¦, ¿¡½ºÆ®·Î°Õ, °æ±¸¿ë ÇÇÀÓ¾à, Æä´ÏÅäÀÎ, ´ÏÄÚÆ¾»ê, ±³°¨½Å°æ¾à, Ä®½·Ã¤³Î±æÇ×Á¦, ±×¸®°í À̼ҴϾÆÁöµå µîÀÌ´Ù. º»Á¦¸¦ º¹¿ëÇϴ ȯÀÚ¿¡°Ô ÀÌ·¯ÇÑ ¾à¹°À» Åõ¿©ÇÑ °æ¿ì, ÀûÀýÇÑ Ç÷´çÁ¶ÀýÀ» À¯ÁöÇϱâ À§ÇØ È¯ÀÚ¸¦ ÀÚ¼¼È÷ °üÂûÇØ¾ß ÇÑ´Ù. °Ç°ÇÑ Áö¿øÀÚ¿¡ ´ëÇÑ ´Üȸ º´¿ëÅõ¿© ¿¬±¸¿¡¼ ÀÌ ¾à°ú ÇÁ·ÎÇÁ¶ó³î·Ñ, ¸ÞÆ®Æ÷¸£¹Î°ú À̺ÎÇÁ·ÎÆæÀÇ ¾à¹°µ¿·ÂÇÐÀû ¼ºÁúÀº ¼·Î ¿µÇâÀ» ¹ÞÁö ¾Ê´Â´Ù. º»Á¦°¡ Ç÷Àå ´Ü¹éÁú°ú °áÇÕÇÏ´Â °ÍÀº ¹«½ÃÇØµµ ÁÁÀ» ¸¸ÅÀ̹ǷÎ, Ç÷Àå´Ü¹éÁú°ú ±¤¹üÀ§ÇÏ°Ô °áÇÕÇÏ´Â ¼³Æ÷´Ò¿ì·¹¾Æ¿Í ºñ±³ÇÒ ¶§, »ì¸®½Ç»ê, ¼³Æù¾Æ¹Ìµå, Ŭ·Î¶÷Æä´ÏÄݰú ÇÁ·Îº£³×½Ãµå¿Í °°ÀÌ ´Ü¹éÁú°ú ´Ù·® °áÇÕÇÏ´Â ¾à¹°°ú´Â »óÈ£ÀÛ¿ëÀÌ Àû´Ù.
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(metformin; )
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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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º´¿ë±Ý±â :
[ethyl esters of the iodised fatty acids of poppyseed oil]
[iobitridol]
[iodixanol]
[iodixanol]
[iohexol]
[iohexol]
[iohexol]
[iomeprol]
[iopamidol]
[iopromide]
[ioversol]
[»óÈ£ÀÛ¿ë/º´¿ë±Ý±â°Ë»ö]
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°í½ÃµÈ ¿¬·É±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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Metformin¿¡ ´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 |
Gliclazide¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Gliclazide binds to the beta cell sulfonyl urea receptor (SUR1). This binding subsequently blocks the ATP sensitive potassium channels. The binding results in closure of the channels and leads to a resulting decrease in potassium efflux leads to depolarization of the beta cells. This opens voltage-dependent calcium channels in the beta cell resulting in calmodulin activation, which in turn leads to exocytosis of insulin containing secretorty granules.
Metformin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Metformin's pharmacologic mechanisms of action are different from other classes of oral antihyperglycemic agents. Metformin decreases hepatic glucose production, decreases intestinal absorption of glucose, and improves insulin sensitivity by increasing peripheral glucose uptake and utilization.
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| Pharmacology |
Gliclazide¿¡ ´ëÇÑ Pharmacology Á¤º¸ Gliclazide is a second generation sulphonylurea which acts as a hypoglycemic agent. It stimulates beta cells of the islet of Langerhans in the pancreas to release insulin. It also enhances peripheral insulin sensitivity. Overall it potentiates insulin release and improves insulin dynamics.
Metformin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Metformin is an antihyperglycemic agent, which improves glucose tolerance in patients with type 2 diabetes, lowering both basal and postprandial plasma glucose. Metformin is not chemically or pharmacologically related to any other classes of oral antihyperglycemic agents. Unlike sulfonylureas, metformin does not produce hypoglycemia in either patients with type 2 diabetes or normal subjects and does not cause hyperinsulinemia. With metformin therapy, insulin secretion remains unchanged while fasting insulin levels and daylong plasma insulin response may actually decrease.
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| Absorption |
Gliclazide¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly and well absorbed but may have wide inter- and intra-individual variability.
Metformin¿¡ ´ëÇÑ Absorption Á¤º¸ Absorbed over 6 hours, bioavailability is 50 to 60% under fasting conditions. Food delays absorption.
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| Toxicity |
Gliclazide¿¡ ´ëÇÑ Toxicity Á¤º¸ LD50=3000 mg/kg (orally in mice)
Metformin¿¡ ´ëÇÑ Toxicity Á¤º¸ Acute oral toxicity (LD50): 350 mg/kg [Rabbit]. It would be expected that adverse reactions of a more intense character including epigastric discomfort, nausea, and vomiting followed by diarrhea, drowsiness, weakness, dizziness, malaise and headache might be seen.
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| Drug Interactions |
Gliclazide¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Acebutolol The beta-blocker decreases the symptoms of hypoglycemiaAtenolol The beta-blocker decreases the symptoms of hypoglycemiaBetaxolol The beta-blocker decreases the symptoms of hypoglycemiaBevantolol The beta-blocker decreases the symptoms of hypoglycemiaBisoprolol The beta-blocker decreases the symptoms of hypoglycemiaCarteolol The beta-blocker decreases the symptoms of hypoglycemiaCarvedilol The beta-blocker decreases the symptoms of hypoglycemiaEsmolol The beta-blocker decreases the symptoms of hypoglycemiaLabetalol The beta-blocker decreases the symptoms of hypoglycemiaMetoprolol The beta-blocker decreases the symptoms of hypoglycemiaNadolol The beta-blocker decreases the symptoms of hypoglycemiaOxprenolol The beta-blocker decreases the symptoms of hypoglycemiaPenbutolol The beta-blocker decreases the symptoms of hypoglycemiaPindolol The beta-blocker decreases the symptoms of hypoglycemiaPractolol The beta-blocker decreases the symptoms of hypoglycemiaPropranolol The beta-blocker decreases the symptoms of hypoglycemiaSotalol The beta-blocker decreases the symptoms of hypoglycemiaTimolol The beta-blocker decreases the symptoms of hypoglycemiaAspirin The salicylate increases the effect of sulfonylureaBismuth Subsalicylate The salicylate increases the effect of sulfonylureaSalicylate-magnesium The salicylate increases the effect of sulfonylureaSalicylate-sodium The salicylate increases the effect of sulfonylureaSalsalate The salicylate increases the effect of sulfonylureaTrisalicylate-choline The salicylate increases the effect of sulfonylureaRepaglinide Similar mode of action - questionable associationRifampin Rifampin decreases the effect of sulfonylureaTranylcypromine The MAO inhibitor increases the effect of the hypoglycemic agentPhenelzine The MAO inhibitor increases the effect of the hypoglycemic agentIsocarboxazid The MAO inhibitor increases the effect of the hypoglycemic agentPhenylbutazone Phenylbutazone increases the effect of the hypoglycemic agentGlucosamine Possible hyperglycemiaDicumarol The agent increases the effect of sulfonylureaChloramphenicol The agent increases the effect of sulfonylureaClofibrate The agent increases the effect of sulfonylurea
Metformin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Cimetidine Cimetidine increases the effect of metforminGlucosamine Possible hyperglycemia
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Gliclazide¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.Avoid alcohol.
Metformin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Avoid alcohol.Take with food to reduce irritation.
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| Drug Target |
[Drug Target]
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| Description |
Gliclazide¿¡ ´ëÇÑ Description Á¤º¸ An oral sulfonylurea hypoglycemic agent which stimulates insulin secretion. [PubChem]
Metformin¿¡ ´ëÇÑ Description Á¤º¸ A biguanide hypoglycemic agent used in the treatment of non-insulin-dependent diabetes mellitus not responding to dietary modification. Metformin improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. (From Martindale, The Extra Pharmacopoeia, 30th ed, p289)
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| Drug Category |
Gliclazide¿¡ ´ëÇÑ Drug_Category Á¤º¸ Hypoglycemic AgentsSulfonylureas
Metformin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Hypoglycemic Agents
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| Smiles String Canonical |
Gliclazide¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN1CC2CCCC2C1
Metformin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ [H]N=C(N=C(N)N)N(C)C
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| Smiles String Isomeric |
Gliclazide¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN1C[C@@H]2CCC[C@@H]2C1
Metformin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ [H]\N=C(\N=C(\N)N)N(C)C
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| InChI Identifier |
Gliclazide¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H21N3O3S/c1-11-5-7-14(8-6-11)22(20,21)17-15(19)16-18-9-12-3-2-4-13(12)10-18/h5-8,12-13H,2-4,9-10H2,1H3,(H2,16,17,19)/f/h16-17H
Metformin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C4H11N5/c1-9(2)4(7)8-3(5)6/h1-2H3,(H5,5,6,7,8)/f/h7H,5-6H2/b7-4-
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| Chemical IUPAC Name |
Gliclazide¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 1-(3,3a,4,5,6,6a-hexahydro-1H-cyclopenta[c]pyrrol-2-yl)-3-(4-methylphenyl)sulfonylurea
Metformin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3-(diaminomethylidene)-1,1-dimethylguanidine
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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