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Mechanism of Action
Cefaclor¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Cefaclor, like the penicillins, is a beta-lactam antibiotic. By binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, it inhibits 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 cefaclor interferes with an autolysin inhibitor.
Pharmacology
Cefaclor¿¡ ´ëÇÑ Pharmacology Á¤º¸ Cefaclor is a second generation cephalosporin antibiotic with a spectrum resembling first-generation cephalosporins. In vitro tests demonstrate that the bactericidal action of the cephalosporins results from inhibition of cell-wall synthesis. Cefaclor has been shown to be active against most strains of the following microorganisms, both in vitro and in clinical infections: Gram positive aerobes - Staphylococci (including coagulase-positive, coagulase-negative, and penicillinase-producing strains), Streptococcus pneumoniae , and Streptococcus pyogenes (group A ©¬-hemolytic streptococci). Gram-negative aerobes - Escherichia coli , Haemophilus influenzae (including ©¬-lactamase-producing ampicillin-resistant strains), Klebsiella sp , and Proteus mirabilis .
Absorption
Cefaclor¿¡ ´ëÇÑ Absorption Á¤º¸ Well absorbed after oral administration, independent of food intake.
Pharmacokinetics
CefaclorÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
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´Ü¹é°áÇÕ : 25%
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Toxicity
Cefaclor¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include diarrhea, nausea, stomach upset, and vomiting.
Drug Interactions
Cefaclor¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Probenecid Probenecid increases the antibiotic's level
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Drug Target
[Drug Target]
Description
Cefaclor¿¡ ´ëÇÑ Description Á¤º¸ Semisynthetic, broad-spectrum antibiotic derivative of cephalexin. [PubChem]
Dosage Form
Cefaclor¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralPowder OralPowder, for solution OralPowder, for suspension OralSuspension Oral
Drug Category
Cefaclor¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsCephalosporins
Smiles String Canonical
Cefaclor¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ NC(C(=O)NC1C2SCC(Cl)=C(N2C1=O)C(O)=O)C1=CC=CC=C1
Smiles String Isomeric
Cefaclor¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ N[C@H](C(=O)N[C@H]1[C@H]2SCC(Cl)=C(N2C1=O)C(O)=O)C1=CC=CC=C1
InChI Identifier
Cefaclor¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C15H14ClN3O4S/c16-8-6-24-14-10(13(21)19(14)11(8)15(22)23)18-12(20)9(17)7-4-2-1-3-5-7/h1-5,9-10,14H,6,17H2,(H,18,20)(H,22,23)/t9?,10-,14-/m1/s1/f/h18,22H
Chemical IUPAC Name
Cefaclor¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (6R,7R)-7-[(2-amino-2-phenylacetyl)amino]-3-chloro-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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