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Dicloxacillin information


Dicloxacillin
Clinical data
AHFS/Drugs.comMonograph
MedlinePlusa685017
Pregnancy
category
  • AU: B2
Routes of
administration
Oral
ATC code
  • J01CF01 (WHO) QJ51CF01 (WHO)
Legal status
Legal status
  • AU: S4 (Prescription only)
  • US: ℞-only
Pharmacokinetic data
Bioavailability60 to 80%
Protein binding98%
MetabolismHepatic
Elimination half-life0.7 hours
ExcretionRenal and biliary
Identifiers
IUPAC name
  • (2S,5R,6R)-6-{[3-(2,6-dichlorophenyl)-5-methyl-
    oxazole-4-carbonyl]amino}-3,3-dimethyl-7-oxo-4-thia-
    1-azabicyclo[3.2.0]heptane-2-carboxylic acid
CAS Number
  • 3116-76-5 checkY
PubChem CID
  • 18381
DrugBank
  • DB00485 checkY
ChemSpider
  • 17358 checkY
UNII
  • COF19H7WBK
KEGG
  • D02348 checkY
ChEBI
  • CHEBI:4511 checkY
ChEMBL
  • ChEMBL893 checkY
CompTox Dashboard (EPA)
  • DTXSID1022924 Edit this at Wikidata
ECHA InfoCard100.019.535 Edit this at Wikidata
Chemical and physical data
FormulaC19H17Cl2N3O5S
Molar mass470.32 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • O=C(O)[C@@H]3N4C(=O)[C@@H](NC(=O)c2c(onc2c1c(Cl)cccc1Cl)C)[C@H]4SC3(C)C
InChI
  • InChI=1S/C19H17Cl2N3O5S/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28)/t13-,14+,17-/m1/s1 checkY
  • Key:YFAGHNZHGGCZAX-JKIFEVAISA-N checkY
  (verify)

Dicloxacillin is a narrow-spectrum β-lactam antibiotic of the penicillin class.[1] It is used to treat infections caused by susceptible (non-resistant) Gram-positive bacteria.[1] It is active against beta-lactamase-producing organisms such as Staphylococcus aureus, which would otherwise be resistant to most penicillins. Dicloxacillin is available under a variety of trade names including Diclocil (BMS).[2]

It was patented in 1961 and approved for medical use in 1968.[3] It is available as a generic medication.[4]

  1. ^ a b Product Information: DICLOXACILLIN SODIUM-dicloxacillin sodium capsule. Teva Pharmaceuticals USA Inc, Revised 8/2015
  2. ^ Miranda-Novales G, Leaños-Miranda BE, Vilchis-Pérez M, Solórzano-Santos F (October 2006). "In vitro activity effects of combinations of cephalothin, dicloxacillin, imipenem, vancomycin and amikacin against methicillin-resistant Staphylococcus spp. strains". Annals of Clinical Microbiology and Antimicrobials. 5: 25. doi:10.1186/1476-0711-5-25. PMC 1617116. PMID 17034644.
  3. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 491. ISBN 9783527607495.
  4. ^ "Competitive Generic Therapy Approvals". U.S. Food and Drug Administration (FDA). 29 June 2023. Archived from the original on 29 June 2023. Retrieved 29 June 2023.

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