28221

Oxacillin sodium salt

815-950 μg/mg (Oxacillin)

• Synonym(s): Sodium 5-methyl-3-phenyl-4-isoxazolyl penicillin
• Empirical Formula (Hill Notation): C₁₉H₁₈N₃NaO₅S
• CAS Number: 1173-88-2
• Molecular Weight: 423.42
• Beilstein: 4098179
• EC Number: 214-636-3
• MDL number: MFCD00082382
• UNSPSC Code: 51283505
• PubChem Substance ID: 57648295
• NACRES: NA.85

Properties

• biological source: synthetic
• form: powder
• concentration: 815-950 μg/mg (Oxacillin)
• color: white to off-white
• antibiotic activity spectrum: Gram-negative bacteria; Gram-positive bacteria
• Mode of action: cell wall synthesis | interferes
• storage temp.: 2-8°C
• SMILES string: [Na+].Cc1onc(-c2ccccc2)c1C(=O)N[C@H]3C4SC(C)(C)[C@@H](N4C3=O)C([O-])=O
• InChI: 1S/C19H19N3O5S.Na/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);/q;+1/p-1/t13-,14+,17?;/m1./s1
• InChI key: VDUVBBMAXXHEQP-ZTRPPZFVSA-M

Description

General description

Chemical structure: ß-lactam

Application

Oxacillin is used to study mechanisms of penicillinase resistance and antimicrobial susceptibility . It has been used to study autolysins

Biochem/physiol Actions

Oxacillin inhibits bacterial cell wall biosynthesis at the level of transpeptidation (PBP) of peptidoglycan. Used to study mechanisms of penicillinase resistance.

Packaging

1g, 5g

Other Notes

Keep container tightly closed in a dry and well-ventilated place.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 2
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves