For research use only. Not for therapeutic Use.
Oxacillin Sodium Monohydrate(Cat No.:A000938)is a beta-lactam antibiotic in the penicillin class, widely used in bacterial research and pharmaceutical studies. Known for its resistance to penicillinase, this compound is effective against penicillinase-producing Staphylococcus strains, including some drug-resistant bacteria. Its monohydrate form ensures stability and solubility, making it ideal for various experimental applications. With a reliable antibacterial profile, Oxacillin Sodium Monohydrate is instrumental in analyzing bacterial resistance mechanisms and developing targeted treatments for staphylococcal infections, contributing to advancements in microbiological and pharmacological research.
Catalog Number | A000938 |
CAS Number | 7240-38-2 |
Synonyms | Methicillin |
Molecular Formula | C19H18N3O5S.Na.H2O |
Purity | ≥95% |
Documentation | |
Target | Bacterial |
Storage | 3 years -20C powder |
IUPAC Name | sodium;(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-carboxylate;hydrate |
InChI | InChI=1S/C19H19N3O5S.Na.H2O/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);;1H2/q;+1;/p-1/t13-,14+,17-;;/m1../s1 |
InChIKey | ZVIYWUUZWWBNMB-VICXVTCVSA-M |
SMILES | CC1=C(C(=NO1)C2=CC=CC=C2)C(=O)N[C@H]3[C@@H]4N(C3=O)[C@H](C(S4)(C)C)C(=O)[O-].O.[Na+] |
Reference | <p>Guzmán, Flavio, MD. /Beta Lactams Antibiotics (penicillins and Cephalosporins) Mechanism of Action.” <em>Medical Pharmacology</em>. Pharmacology Corner, 29 Nov. 2008. Web. 21 Aug. 2012.</p><p>Pitout JD, Sanders CC, Sanders WE Jr. Antimicrobial resistance with focus on beta-lactam resistance in gram-negative bacilli. Am J Med 1997; 103:51.</p></span></p> |