Oxacillin (sodium monohydrate)
Oxacillin sodium monohydrate is an antibiotic similar to Flucloxacillin used in resistant staphylococci infections study[1].
Product Specifications
CAS Number
[7240-38-2]
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
Antibiotic; Bacterial
Type
Reference compound
Related Pathways
Anti-infection
Applications
COVID-19-immunoregulation
Field of Research
Infection
Assay Protocol
https://www.medchemexpress.com/Oxacillin-sodium-monohydrate.html
Purity
99.62
Solubility
DMSO : 50 mg/mL (ultrasonic) |H2O : ≥ 100 mg/mL
Smiles
O=C(O[Na])[C@@H]1N(C2=O)[C@]([C@@H]2NC(C(C(C3=CC=CC=C3)=NO4)=C4C)=O)([H])SC1(C)C.O
Molecular Formula
C19H20N3NaO6S
Molecular Weight
441.43
Precautions
H302, H315, H319, H335
References & Citations
[1]Alexandros Ikonomidis, et al. In vitro and in vivo evaluations of oxacillin efficiency against mecA-positive oxacillin-susceptible Staphylococcus aureus. Antimicrob Agents Chemother. 2008 Nov;52 (11) :3905-8.|[2]R H Raynor, et al. Oxacillin-induced lysis of Staphylococcus aureus. Antimicrob Agents Chemother. 1979 Aug;16 (2) :134-40.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Scientific Category
Reference compound1
Clinical Information
Launched
Citation 01
ACS Omega. 2022 Mar 3;7 (10) :9004-9014.|AMB Express. 2024 Dec 24;14 (1) :141.|bioRxiv. 2024 May 10.|bioRxiv. 2025 Oct 27.|BMC Microbiol. 2023 Apr 20;23 (1) :109.|Emerg Microbes Infect. 2024 Dec;13 (1) :2321981.|iScience. 2022 Jan 5;25 (2) :103731.|Microbiol Spectr. 2022 Apr 27;10 (2) :e0054121.|Research Square Print. December 5th, 2022.|Biomed Res Int. 2018 Jul 2:2018:3579832.|Front Microbiol. 2020 Jul 31:11:1720.|Curr Microbiol. 2023 May 31;80 (7) :230.|Microorganisms. 2024 Jan 25;12 (2) :256.
Available Sizes
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