Oxacillin: Difference between revisions
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imported>David E. Volk (New page: {{subpages}} right|thumb|250px|{{#ifexist:Template:Oxacillin structure.jpg/credit|{{Oxacillin structure.jpg/credit}}<br/>|}}Oxacillin. '''Oxacillin''', s...) |
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Its IUPAC chemical name is (2S,5R,6R)-3,3-dimethyl-6-[(5-methyl-3-phenyl1,2-oxazole-4-carbonyl)amino]-7-oxo-4- | Its IUPAC chemical name is (2S,5R,6R)-3,3-dimethyl-6-[(5-methyl-3-phenyl1,2-oxazole-4-carbonyl)amino]-7-oxo-4- | ||
thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid and it has molecular formula C<sub>19</sub>H<sub>19</sub>N<sub>3</sub>O<sub>5</sub>S. | thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid and it has molecular formula C<sub>19</sub>H<sub>19</sub>N<sub>3</sub>O<sub>5</sub>S. | ||
== External links == | |||
* {{DailyMed}} | |||
* Drug Bank [http://www.drugbank.ca/cgi-bin/getCard.cgi?CARD=DB00713.txt] | |||
Revision as of 11:32, 11 February 2008
Oxacillin, sold under the brand name Bactocill®, is a penicillin beta-lactam type of antibiotic similar to flucloxacillin used in resistant staphylococci infections. It is active against gram-positive bacteria and some gram-negative bacteria. Like other penicillin-like antibiotics, it functions by interfering with the last stage of bacterial cell wall synthesis and leads to autolysis of the bacteria cells. It is stable against hydrolysis from beta-lactamases, including penicillinases, and cephalosporinases.
Its IUPAC chemical name is (2S,5R,6R)-3,3-dimethyl-6-[(5-methyl-3-phenyl1,2-oxazole-4-carbonyl)amino]-7-oxo-4- thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid and it has molecular formula C19H19N3O5S.
External links
- Oxacillin - FDA approved drug information (drug label) from DailyMed (U.S. National Library of Medicine).
- Drug Bank [1]