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(amoxicillin; )
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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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AmoxicillinÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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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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ÀüÈ: 02-3486-1061 ¤Ó À̸ÞÀÏ: webmaster@druginfo.co.kr
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