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QuickView for cefalexin (compound)


PubChem
Name: Cephalexin
PubChem Compound ID: 10521584
Description: 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.
Molecular formula: C16H17N3O4S
Molecular weight: 347.39 g/mol
DrugBank
Identification
Name: Cephalexin
Name (isomeric): DB00567
Drug Type: small molecule
Description: 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.
Synonyms:
Cefalexin Sodium; Cefalexina [INN-Spanish]; Cephalexin monohydrate; Cefalexin; Cephalexin 1-hydrate; Cephalexinum; Cefalessina [DCIT]; Cephalexine; Cephalexin hydrate; CEX.
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Brand: Neolexina, Cefadal, Kekrinal, Tokiolexin, Ceporexin, Sinthecillin, Ibrexin, Voxxim, Ortisporina, Roceph, Alsporin, Syncle, Madlexin, Sartosona, Oracef, Ceforal, Mamalexin, Fexin, Sporicef, Nufex, Cophalexin, Kidolex, Oroxin, Neokef, Zozarine, Uphalexin, Sialexin, Sencephalin, Keflex, Sporidex, Novolexin, Cefadin, Mamlexin, Lonflex, Cefadina, Keftab, Pyassan, Celexin, Syncl, Ceporex, Carnosporin, L-Keflex, Cefovit, Ceporex Forte, Panixine Disperdose, Ceporexin-E, Keflet, Cefax, Cefaleksin, Cefaloto, Durantel DS, Factagard, Cepol, Ed A-Ceph, Sepexin, Palitrex, Cepexin, Lopilexin, Erocetin, Cepastar, Cephaxin, Sanaxin, Ibilex, Pectril, Medoxine, Cephin, Alexin, Larixin, Lafarine, Check, Lenocef, Cefablan, Cefa-iskia, Cefalin, Servispor, Tepaxin, Cephanasten, Inphalex, Keforal, Biocef, Kefalospes, Kefolan, Felexin, Ceporexine, Alcephin, Durantel, Winlex, Synecl, Ospexin, Oriphex, Lexibiotico, Cefaseptin, Cephacillin
Category: Cephalosporins, Anti-Bacterial Agents
CAS number: 15686-71-2
Pharmacology
Indication: For the treatment of respiratory tract infections caused by <i>Streptococcus pneumoniae</i> and <i>Streptococcus pyogenes</i>; otitis media due to <i>Streptococcus pneumoniae</i>, <i>Haemophilus influenzae</i>, <i>Staphylococcus aureus</i>, <i>Streptococcus pyogenes</i>, and <i>Moraxella catarrhalis</i>; skin and skin structure infections caused by <i>Staphylococcus aureus</i> and/or <i>Streptococcus pyogenes</i>; bone infections caused by <i>Staphylococcus aureus</i> and/or <i>Proteus mirabilis</i>; genitourinary tract infections, including acute prostatitis, caused by <i>Escherichia coli</i>, <i>Proteus mirabilis</i>, and <i>Klebsiella pneumoniae</i>.
Pharmacology: 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.
Mechanism of Action:
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 cephalexi...
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Absorption: Well absorbed from the gastrointestinal tract
Protein binding: 14%
Biotransformation: No appreciable biotransformation in the liver (90% of the drug is excreted unchanged in the urine).
Route of elimination: Cephalexin is excreted in the urine by glomerular filtration and tubular secretion. Studies showed that over 90% of the drug was excreted unchanged in the urine within 8 hours.
Half Life: 1 hour
Toxicity: 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.
Affected organisms: Enteric bacteria and other eubacteria
Interactions
Food interaction:
Take on empty stomach: 1 hour before or 2 hours after meals.
Drug interaction:
ProbenecidProbenecid may increase the serum level of cephalexin.

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