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1.5 mL |
1.7 mL |
5.0 mL |
5.2 mL |
| 500 mg |
2.5 mL |
2.9 mL |
10.0 mL |
10.4 mL |
| 1000 mg |
2.5 mL |
3.3 mL |
20.0 mL |
20.8 mL |
3. ÁÖ»ç¿ë¼ö¿¡ ¿ëÇØ½ÃŲ ÈÄ ÀϽÃÀûÀ¸·Î »öÀÇ º¯È°¡ ÀϾ ¼ö ÀÖ´Ù.
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Amoxicillin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Amoxicillin binds to penicillin-binding protein 1A (PBP-1A) located inside the bacterial cell well. Penicillins acylate the penicillin-sensitive transpeptidase C-terminal domain by opening the lactam ring. This inactivation of the enzyme prevents the formation of a cross-link of two linear peptidoglycan strands, inhibiting the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that amoxicllin interferes with an autolysin inhibitor.
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| Pharmacology |
Amoxicillin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Amoxicillin is a moderate-spectrum antibiotic active against a wide range of Gram-positive, and a limited range of Gram-negative organisms. It is usually the drug of choice within the class because it is better absorbed, following oral administration, than other beta-lactam antibiotics. Amoxicillin is susceptible to degradation by ¥â-lactamase-producing bacteria, and so may be given with clavulanic acid to increase its susceptability. The incidence of ¥â-lactamase-producing resistant organisms, including E. coli, appears to be increasing. Amoxicillin is sometimes combined with clavulanic acid, a ¥â-lactamase inhibitor, to increase the spectrum of action against Gram-negative organisms, and to overcome bacterial antibiotic resistance mediated through ¥â-lactamase production.
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| Metabolism |
Amoxicillin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 2C19 (CYP2C19)
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| Protein Binding |
Amoxicillin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ In blood serum, amoxicillin is approximately 20% protein-bound
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| Half-life |
Amoxicillin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 61.3 minutes
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| Absorption |
Amoxicillin¿¡ ´ëÇÑ Absorption Á¤º¸ Rapidly absorbed after oral administration.
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| Pharmacokinetics |
Amoxicillin sodiumÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Èí¼ö : °æ±¸ : ºü¸£°í °ÅÀÇ ¿ÏÀúÈ÷ Èí¼öµÈ´Ù. À½½Ä¹°Àº Èí¼ö¿¡ ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê´Â´Ù.
- ºÐÆ÷ : ³úô¼ö¾×°ú Ç÷¾×°£ÀÇ ³óµµºñ :
- Á¤»ó ³ú¸· : 1% ÀÌÇÏ
- ¿°Áõ¼º ³ú¸· : 8-90%
- ´Ü¹é°áÇÕ : 17-20%
- ´ë»ç : ºÎºÐÀû
- ¹Ý°¨±â :
- ½Å»ý¾Æ : 3.7½Ã°£
- ¿µ¾Æ ¹× ¼Ò¾Æ : 1-2 ½Ã°£
- Á¤»ó ½Å±â´ÉÀ» °¡Áø ¼ºÀÎ : 0.7-1.4 ½Ã°£
- CLcr < 10 mL/minÀΠȯÀÚ : 7-21 ½Ã°£
- Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 2½Ã°£ (ݼ¿Á¦), 1½Ã°£ (Çöʾ×)
- ¼Ò½Ç : ½Å¹è¼³ (80%°¡ ¹Ì´ë»çü·Î)
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| Biotransformation |
Amoxicillin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic metabolism accounts for less than 30% of the biotransformation of most penicillins
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| Toxicity |
Amoxicillin¿¡ ´ëÇÑ Toxicity Á¤º¸ Serious toxicity is unlikely following large doses of amoxicillin. Acute ingestion of large doses of amoxicillin may cause nausea, vomiting, diarrhea and abdominal pain. Acute oliguric renal failure and hematuria may occur following large doses.
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| Drug Interactions |
Amoxicillin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Methotrexate The penicillin increases the effect and toxicity of methotrexateDemeclocycline Possible antagonism of actionDoxycycline Possible antagonism of actionEthinyl Estradiol This anti-infectious agent could decrease the effect of the oral contraceptiveMethacycline Possible antagonism of actionMinocycline Possible antagonism of actionOxytetracycline Possible antagonism of actionRolitetracycline Possible antagonism of actionTetracycline Possible antagonism of actionMestranol This anti-infectious agent could decrease the effect of the oral contraceptive
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Amoxicillin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take without regard to meals.
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| Drug Target |
[Drug Target]
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| Description |
Amoxicillin¿¡ ´ëÇÑ Description Á¤º¸ A broad-spectrum semisynthetic antibiotic similar to ampicillin except that its resistance to gastric acid permits higher serum levels with oral administration. [PubChem]
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| Dosage Form |
Amoxicillin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralPowder, for solution OralPowder, for suspension OralSuspension OralTablet Oral
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| Drug Category |
Amoxicillin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsPenicillins
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| Smiles String Canonical |
Amoxicillin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1(C)SC2C(NC(=O)C(N)C3=CC=C(O)C=C3)C(=O)N2C1C(O)=O
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| Smiles String Isomeric |
Amoxicillin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)C3=CC=C(O)C=C3)C(=O)N2[C@H]1C(O)=O
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| InChI Identifier |
Amoxicillin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C16H19N3O5S/c1-16(2)11(15(23)24)19-13(22)10(14(19)25-16)18-12(21)9(17)7-3-5-8(20)6-4-7/h3-6,9-11,14,20H,17H2,1-2H3,(H,18,21)(H,23,24)/t9-,10-,11+,14-/m1/s1/f/h18,23H
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| Chemical IUPAC Name |
Amoxicillin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (2S,5R,6R)-6-[[(2R)-2-amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
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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
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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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The database contains the following fields: The generic name of each chemical For module A10 (liver enzyme composite module): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the number of active and marginally active scores for each compound at the five individual endpoints (see research article for full description of method) Number of endpoints at which each compound is marginally active (M) Number of endpoints at which each compound is active (A) For modules A11 to A15 (alkaline phosphatase increased, SGOT increased, SGPT increased, LDH increased, and GGT increased, respectively): Overall activity category for each compound (A for active, M for marginally active, or I for inactive) based on the RI and ADR values (see the research article for full description of method) Number of ADR reports for each compound, given as <4 or ¡Ã4 Reporting Index value for each compound, except where no shipping units were available (NSU) Group 1 comprises of compounds for which ADR data were available for the first five years of marketing, so when no ADR reports were listed during this period the compounds were evaluated as inactive. Group 2 comprises of compounds for which a 'steady state' period of ADR data were available (1992-1996). In cases where no ADR reports were filed during this period, the compounds were scored as 'NA' (data not available) since they may have had one or more ADR reports during their first five years of marketing which should not be negated by a lack of ADR reports during the steady-state period. AMOXICILLIN[GGT Increase][Composite Activity](Score) I(Marginal) 0(Active) 0[Alkaline Phosphatase Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[SGOT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0.1[SGPT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[LDH Increase](Activity Score) I(Number of Rpts) <4(Index value) 0[GGT Increase](Activity Score) I(Number of Rpts) <4(Index value) 0
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