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Pharmacokinetics
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Cephalexin ¿¡ ´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
Cephalexin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Cephalexin, 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 cephalexin interferes with an autolysin inhibitor.
Pharmacology
Cephalexin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Cephalexin (also called Cefalexin) is a first generation cephalosporin antibiotic. It is one of the most widely prescribed antibiotics, often used for the treatment of superficial infections that result as complications of minor wounds or lacerations. It is effective against most gram-positive bacteria.
Protein Binding
Cephalexin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 14%
Half-life
Cephalexin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 1 hour
Absorption
Cephalexin¿¡ ´ëÇÑ Absorption Á¤º¸ Well absorbed from the gastrointestinal tract
Pharmacokinetics
Methylol Cephalexin LysinateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
Cephalexin :
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ÅÂ¹Ý Åë°ú, À¯Áó ºÐÆ÷
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3-12°³¿ùÀÇ ¼Ò¾Æ : 2.5 ½Ã°£
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Methylol cephalexin lysinate´Â cephalexinº¸´Ù ¹Ý°¨±â°¡ ´õ ±æ´Ù°í Á¦Á¶È¸»ç¿¡¼´Â º¸°íÇÏ¿´´Ù.
Ç÷ÁßÃÖ°í³óµµ µµ´Þ½Ã°£ : °æ±¸ : 1½Ã°£ À̳»
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Biotransformation
Cephalexin¿¡ ´ëÇÑ Biotransformation Á¤º¸ No appreciable biotransformation in the liver (90% of the drug is excreted unchanged in the urine).
Toxicity
Cephalexin¿¡ ´ëÇÑ Toxicity Á¤º¸ Symptoms of overdose include blood in the urine, diarrhea, nausea, upper abdominal pain, and vomiting. The oral median lethal dose of cephalexin in rats is >5000 mg/kg.
Drug Interactions
Cephalexin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Probenecid Probenecid increases the antibiotic's level
CYP450 Drug Interaction
[CYP450 TableÁ÷Á¢Á¶È¸]
Food Interaction
Cephalexin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take on empty stomach: 1 hour before or 2 hours after meals.
Drug Target
[Drug Target]
Description
Cephalexin¿¡ ´ëÇÑ Description Á¤º¸ A semisynthetic cephalosporin antibiotic with antimicrobial activity similar to that of cephaloridine or cephalothin, but somewhat less potent. It is effective against both gram-positive and gram-negative organisms. [PubChem]
Dosage Form
Cephalexin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralPowder, for solution OralPowder, for suspension OralSuspension OralTablet Oral
Drug Category
Cephalexin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsCephalosporins
Smiles String Canonical
Cephalexin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC1=C(N2C(SC1)C(NC(=O)C(N)C1=CC=CC=C1)C2=O)C(O)=O
Smiles String Isomeric
Cephalexin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ CC1=C(N2[C@H](SC1)[C@H](NC(=O)[C@H](N)C1=CC=CC=C1)C2=O)C(O)=O
InChI Identifier
Cephalexin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C16H17N3O4S/c1-8-7-24-15-11(14(21)19(15)12(8)16(22)23)18-13(20)10(17)9-5-3-2-4-6-9/h2-6,10-11,15H,7,17H2,1H3,(H,18,20)(H,22,23)/t10-,11-,15-/m1/s1/f/h18,22H
Chemical IUPAC Name
Cephalexin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ (6R,7R)-7-[[(2R)-2-amino-2-phenylacetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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