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¼¼ÆÄ³ªÁÖ500mg(¸ÞÄ¥¿Ã¼¼ÆÈ·º½Å¸®Áö³×ÀÌÆ®) [Methylol Cephalexin Lysinate]
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663603230[A62750921]
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1¼¼´ë ¼¼ÆÈ·Î½ºÆ÷¸°°è (Cephalosporins; First Generation)
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| DUR (ÀǾàǰ»ç¿ëÆò°¡) |
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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.
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| 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.
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| Protein Binding |
Cephalexin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 14%
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| Half-life |
Cephalexin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 1 hour
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| Absorption |
Cephalexin¿¡ ´ëÇÑ Absorption Á¤º¸ Well absorbed from the gastrointestinal tract
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| Pharmacokinetics |
Methylol Cephalexin LysinateÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á
- Cephalexin :
- Èí¼ö : ¾î¸° ¼Ò¾Æ¿¡¼´Â Áö¿¬µÈ´Ù. ½Å»ý¾Æ¿¡¼ 50%±îÁö Èí¼ö°¡ °¨¼ÒÇÒ ¼ö ÀÖ´Ù.
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- ³úô¼ö¾×À¸·ÎÀÇ ºÐÆ÷´Â ¹Ì¹ÌÇÏ´Ù.
- ÅÂ¹Ý Åë°ú, À¯Áó ºÐÆ÷
- ´Ü¹é°áÇÕ : 6-15%
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- 3-12°³¿ùÀÇ ¼Ò¾Æ : 2.5 ½Ã°£
- ¼ºÀÎ : 0.5-1.2 ½Ã°£ (½ÅÀå¾Ö½Ã ¿¬Àå)
- 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»
- ¼Ò½Ç : 8½Ã°£ À̳»¿¡ 80-100%°¡ ¹Ìº¯Èü·Î ½Å¹è¼³
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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).
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| 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.
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| Drug Interactions |
Cephalexin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Probenecid Probenecid increases the antibiotic's level
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CYP450 Drug Interaction |
[CYP450 TableÁ÷Á¢Á¶È¸]
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| Food Interaction |
Cephalexin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Take on empty stomach: 1 hour before or 2 hours after meals.
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| Drug Target |
[Drug Target]
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| 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]
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| Dosage Form |
Cephalexin¿¡ ´ëÇÑ Dosage_Form Á¤º¸ Capsule OralPowder, for solution OralPowder, for suspension OralSuspension OralTablet Oral
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| Drug Category |
Cephalexin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Anti-Bacterial AgentsCephalosporins
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| 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
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| 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
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| 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
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| 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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