Our website is made possible by displaying online advertisements to our visitors.
Please consider supporting us by disabling your ad blocker.

Responsive image


Oxacillin

Oxacillin
Clinical data
Trade namesBactocill
AHFS/Drugs.comMonograph
MedlinePlusa685020
ATC code
Identifiers
  • (2S,5R,6R)-3,3-dimethyl-6-[(5-methyl-3-phenyl-
    1,2-oxazole-4-carbonyl)amino]-7-oxo-4-thia-1-
    azabicyclo[3.2.0]heptane-2-carboxylic acid
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.000.577 Edit this at Wikidata
Chemical and physical data
FormulaC19H19N3O5S
Molar mass401.44 g·mol−1
3D model (JSmol)
Density1.49 g/cm3
Boiling point686.8 °C (1,268.2 °F)
  • [H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)C1=C(C)ON=C1C1=CC=CC=C1)C(O)=O
  • InChI=1S/C19H19N3O5S/c1-9-11(12(21-27-9)10-7-5-4-6-8-10)15(23)20-13-16(24)22-14(18(25)26)19(2,3)28-17(13)22/h4-8,13-14,17H,1-3H3,(H,20,23)(H,25,26)/t13-,14+,17-/m1/s1 ☒N
  • Key:UWYHMGVUTGAWSP-JKIFEVAISA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Oxacillin (trade name Bactocill) is a narrow-spectrum second-generation beta-lactam antibiotic of the penicillin class developed by Beecham.[1]

It was patented in 1960 and approved for medical use in 1962.[2]

  1. ^ Greenwood D (2008). Antimicrobial drugs: chronicle of a twentieth century medical triumph. Oxford University Press US. pp. 124–. ISBN 978-0-19-953484-5. Retrieved 18 November 2010.
  2. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 490. ISBN 9783527607495.

Previous Page Next Page






أوكساسيلين Arabic اوقزاسیلین AZB Ocsacilin Sodiwm CY Oxacillin German Oxacilina Spanish اگزاسیلین FA Oxacilline French אוקסצילין HE Oxacillin Hungarian Oksasilin ID

Responsive image

Responsive image