Cefalexin: Difference between revisions

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== Chemistry ==
== Chemistry ==
An [[IUPAC]] chemical name of cefalexin is (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.  Its chemical formula,  C<sub>16</sub>H<sub>17</sub>N<sub>3</sub>O<sub>4</sub>S, gives it an average molecule mass of 347.3890 gram/mole. Its antibacterial activity is due to the core beta-[[lactam]] structure, which bind with penicillin-binding proteins within bacteria, thereby inhibiting bacterial cell wall synthesis, by an acylation reaction of the lactam with the bacterial proteins.
An [[IUPAC]] chemical name of cefalexin is (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.  Its chemical formula,  C<sub>16</sub>H<sub>17</sub>N<sub>3</sub>O<sub>4</sub>S, gives it an average molecule mass of 347.3890 gram/mole. Its antibacterial activity is due to the core beta-[[lactam]] structure, which bind with penicillin-binding proteins within bacteria, thereby inhibiting bacterial cell wall synthesis, by an acylation reaction of the lactam with the bacterial proteins.
== Brand Names ==
{{col-begin|width=100%}}
{{col-break|width=20%}}
Alcephin
Alexin
Alsporin
Biocef
Carnosporin
Cefa-iskia
Cefablan
Cefadal
Cefadin
Cefadina
Cefaleksin
Cefalin
Cefaloto
Cefaseptin
Cefax
Ceforal
Cefovit
Celexin
Cepastar
Cepexin
{{col-break|width=20%}}
Cephacillin
Cephanasten
Cephaxin
Cephin
Cepol
Ceporex
Ceporex Forte
Ceporexin
Ceporexin-E
Ceporexine
Check
Cophalexin
Durantel
Durantel DS
Ed A-Ceph
Erocetin
Factagard
Felexin
Fexin
Ibilex
{{col-break|width=20%}}
Ibrexin
Inphalex
Kefalospes
Keflet
Keflex
Kefolan
Keforal
Keftab
Kekrinal
Kidolex
L-Keflex
Lafarine
Larixin
Lenocef
Lexibiotico
Lonflex
Lopilexin
Madlexin
Mamalexin
Mamlexin
{{col-break|width=20%}}
Medoxine
Neokef
Neolexina
Novolexin
Nufex
Oracef
Oriphex
Oroxin
Ortisporina
Ospexin
Palitrex
Panixine Disperdose
Pectril
Pyassan
Roceph
Sanaxin
Sartosona
Sencephalin
Sepexin
Servispor
{{col-break|width=20%}}
Sialexin
Sinthecillin
Sporicef
Sporidex
Syncl
Syncle
Synecl
Tepaxin
Tokiolexin
Uphalexin
Voxxim
Winlex
Zozarine
{{col-end}}


== References ==
== References ==
<references/>
<references/>
{{CZMed}}
{{CZMed}}

Revision as of 15:17, 13 July 2009

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cefalexin
IUPAC name: see chemistry section
Synonyms: cephalexin
Formula: C16H17N3O4S

 Uses: antibiotic drug

 Properties: beta-lactam

 Hazards: see drug interactions

Mass (g/mol): CAS #:
347.3890 15686-71-2


Cefalexin (cephalexin) is one of the most widely used antibiotic medications. It is a first-generation cephalosporin type of antibiotic drug, that is sold under nearly 100 brand names.

Chemistry

An IUPAC chemical name of cefalexin is (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. Its chemical formula, C16H17N3O4S, gives it an average molecule mass of 347.3890 gram/mole. Its antibacterial activity is due to the core beta-lactam structure, which bind with penicillin-binding proteins within bacteria, thereby inhibiting bacterial cell wall synthesis, by an acylation reaction of the lactam with the bacterial proteins.

Brand Names

Alcephin Alexin Alsporin Biocef Carnosporin Cefa-iskia Cefablan Cefadal Cefadin Cefadina Cefaleksin Cefalin Cefaloto Cefaseptin Cefax Ceforal Cefovit Celexin Cepastar Cepexin

Cephacillin Cephanasten Cephaxin Cephin Cepol Ceporex Ceporex Forte Ceporexin Ceporexin-E Ceporexine Check Cophalexin Durantel Durantel DS Ed A-Ceph Erocetin Factagard Felexin Fexin Ibilex

Ibrexin Inphalex Kefalospes Keflet Keflex Kefolan Keforal Keftab Kekrinal Kidolex L-Keflex Lafarine Larixin Lenocef Lexibiotico Lonflex Lopilexin Madlexin Mamalexin Mamlexin

Medoxine Neokef Neolexina Novolexin Nufex Oracef Oriphex Oroxin Ortisporina Ospexin Palitrex Panixine Disperdose Pectril Pyassan Roceph Sanaxin Sartosona Sencephalin Sepexin Servispor

Sialexin Sinthecillin Sporicef Sporidex Syncl Syncle Synecl Tepaxin Tokiolexin Uphalexin Voxxim Winlex Zozarine

References

The most up-to-date information about Cefalexin and other drugs can be found at the following sites.