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µ¿È¹Ì¶ô½ÃµåÁ¤(ÇǹãÇǽǸ°¿°»êÇǺê¸Þ½Ç¸®³²Á¤) MIRAXID C.TAB.[Pivampicillin , Pivmecillinam HCl]
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ÀÌ¿ëÇÏ½Ç ¼ö ÀÖ½À´Ï´Ù.
À¯·áÁ¤º¸¸ñ·ÏÀº Àü¹®È¸¿øÀ¸·Î
·Î±×ÀÎ ÇϽøé È®ÀÎ °¡´ÉÇÕ´Ï´Ù.
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û±¸ÄÚµå(KDÄÚµå) ºñ±Þ¿©Á¡°ËÄÚµå »óÇÑ±Ý¾× |
642704660[A05702851]
[º¸ÇèÄڵ忡 µû¸¥ ¾àǰ±âº»Á¤º¸ Á÷Á¢Á¶È¸]
\0 ¿ø/1Á¤(2005.09.01)(ÇöÀç¾à°¡)
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100TAB. |
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8806427046605 |
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[Drugbank ÀÇ ¼ººÐÁ¤º¸¿¶÷] [Ampicillin]
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(ampicillin; )
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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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°í½ÃµÈ º´¿ë±Ý±â ³»¿ëÀº ¾ø½À´Ï´Ù.
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Ampicillin¿¡ ´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 |
Pivampicillin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Ampicillin (the active metabolite of pivampicillin) has a bactericidal action resulting from inhibition of cell wall mucopeptide biosynthesis.
Pivmecillinam¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Pivmecillinam interferes with the biosynthesis of the bacterial cell wall however its activity is slightly different from that of other penicillins and cephalosporins
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| Pharmacology |
Pivampicillin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pivampicillin is the pivaloyloxymethyl ester of (the semi-synthetic penicillin) ampicillin. It is an inactive pro-drug, which is converted during its absorption from the gastrointestinal tract to the microbiologically active ampicillin, together with formaldehyde and pivalic acid, by non-specific esterases present in most body tissues. Amounts in excess of 99% of the pivampicillin absorbed are converted to ampicillin within 15 minutes of absorption.
Pivmecillinam¿¡ ´ëÇÑ Pharmacology Á¤º¸ Pivmecillinam is a pivaloyloxymethyl ester of amdinocillin that is well absorbed orally, but broken down to amdinocillin in the intestinal mucosa. It is active against gram-negative organisms and used as for amdinocillin.
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| Half-life |
Pivampicillin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Approximately 1 hour.
Pivmecillinam¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ Not Available
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| Absorption |
Pivampicillin¿¡ ´ëÇÑ Absorption Á¤º¸ Absorbed following oral administration.
Pivmecillinam¿¡ ´ëÇÑ Absorption Á¤º¸ Well absorbed following oral administration.
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| Pharmacokinetics |
Pivmecillinam HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ : 75% ÀÌ»ó
- ´Ü¹é°áÇÕ : 5-10%
- ´ë»ç : Èí¼öµÈ ÈÄ ºü¸£°Ô Ȱ¼º´ë»çüÀÎ mecillinamÀ¸·Î ´ë»çµÈ´Ù.
- ¹Ý°¨±â : 1½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 0.5-1 ½Ã°£ À̳»
- ¼Ò½Ç : 60% ÀÌ»óÀÌ mecillinamÀ¸·Î ½Å¹è¼³µÈ´Ù.
PivampicillinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ :
- µ¿·®À» Åõ¿©ÇßÀ» ¶§ ampicillin Á¦Á¦º¸´Ù Ç÷Áß³óµµ°¡ 2-3 ¹è ´õ ³ô´Ù.
- À½½Ä¹°ÀÌ Èí¼ö¿¡ ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê´Â´Ù.
- ºÐÆ÷ :
- ´ãÁ󳻿¡ ºÐÆ÷
- ¿°Áõ¼º ³ú¸· »óÅ¿¡¼¸¸ ³úô¼ö¾×À¸·Î Àß Åõ°úµÈ´Ù. (ÀϹÝÀûÀ¸·Î MICs ÀÌ»ó)
- ³úô¼ö¾× ´ë Ç÷¾×ÀÇ ³óµµºñ
- Á¤»ó ³ú¸· : 0
- ¿°Áõ¼º ³ú¸· : 5-10%
- ´Ü¹é°áÇÕ : 15-25%
- ´ë»ç : »ýü³»¿¡¼ ºü¸£°Ô ampicillinÀ¸·Î °¡¼öºÐÇØµÈ´Ù.
- ¹Ý°¨±â :
- ½Å»ý¾Æ : 2-7ÀÏ : 4½Ã°£
- 8-14ÀÏ : 2.8½Ã°£
- 15-30ÀÏ : 1.7½Ã°£
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| Biotransformation |
Pivampicillin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Not Available
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| Drug Interactions |
Pivampicillin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Methotrexate The penicillin increases the effect and toxicity of methotrexateDemeclocycline Possible antagonism of actionDoxycycline Possible antagonism of actionTetracycline Possible antagonism of actionRolitetracycline Possible antagonism of actionOxytetracycline Possible antagonism of actionMinocycline Possible antagonism of actionMethacycline Possible antagonism of actionEthinyl Estradiol This anti-infectious agent could decrease the effect of the oral contraceptiveMestranol This anti-infectious agent could decrease the effect of the oral contraceptive
Pivmecillinam¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Demeclocycline Possible antagonism of actionDoxycycline Possible antagonism of actionMethacycline Possible antagonism of actionMinocycline Possible antagonism of actionOxytetracycline Possible antagonism of actionRolitetracycline Possible antagonism of actionTetracycline Possible antagonism of action
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Pivampicillin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.
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| Drug Target |
[Drug Target]
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| Description |
Pivampicillin¿¡ ´ëÇÑ Description Á¤º¸ Pivalate ester analog of ampicillin.
Pivmecillinam¿¡ ´ëÇÑ Description Á¤º¸ Pivaloyloxymethyl ester of amdinocillin that is well absorbed orally, but broken down to amdinocillin in the intestinal mucosa. It is active against gram-negative organisms and used as for amdinocillin. [PubChem]
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| Dosage Form |
Pivampicillin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Tablet Oral
Pivmecillinam¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Not Available
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| Drug Category |
Pivmecillinam¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsAnti-Infective Agents, Urinary
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| Smiles String Canonical |
Pivampicillin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)(C)C(=O)OCOC(=O)C1N2C(SC1(C)C)C(NC(=O)C(N)C1=CC=CC=C1)C2=O
Pivmecillinam¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(C)(C)C(=O)OCOC(=O)C1N2C(SC1(C)C)C(N=CN1CCCCCC1)C2=O
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| Smiles String Isomeric |
Pivampicillin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)(C)C(=O)OCOC(=O)[C@@H]1N2[C@H](SC1(C)C)[C@H](NC(=O)[C@H](N)C1=CC=CC=C1)C2=O
Pivmecillinam¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC(C)(C)C(=O)OCOC(=O)[C@@H]1N2[C@H](SC1(C)C)[C@H](\N=C\N1CCCCCC1)C2=O
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| InChI Identifier |
Pivampicillin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C22H29N3O6S/c1-21(2,3)20(29)31-11-30-19(28)15-22(4,5)32-18-14(17(27)25(15)18)24-16(26)13(23)12-9-7-6-8-10-12/h6-10,13-15,18H,11,23H2,1-5H3,(H,24,26)/t13-,14-,15+,18-/m1/s1/f/h24H
Pivmecillinam¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C21H33N3O5S/c1-20(2,3)19(27)29-13-28-18(26)15-21(4,5)30-17-14(16(25)24(15)17)22-12-23-10-8-6-7-9-11-23/h12,14-15,17H,6-11,13H2,1-5H3/b22-12+/t14-,15?,17-/m1/s1
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| Chemical IUPAC Name |
Pivampicillin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2,2-dimethylpropanoyloxymethyl (2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
Pivmecillinam¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 2,2-dimethylpropanoyloxymethyl (5R,6R)-6-(azepan-1-ylmethylideneamino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
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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.
¹Ýµå½Ã Á¦Á¶¡¤¼öÀÔ»ç, ÆÇ¸Å»ç, ÀÇ»ç, ¾à»ç¿¡°Ô ÃÖÁ¾ÀûÀ¸·Î È®ÀÎÇϽñ⠹ٶø´Ï´Ù.
ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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