28221

Oxacillin sodium salt

815-950 μg/mg (Oxacillin)

• Synonim(y): Sodium 5-methyl-3-phenyl-4-isoxazolyl penicillin
• Wzór empiryczny (zapis Hilla): C₁₉H₁₈N₃NaO₅S
• Numer CAS: 1173-88-2
• Masa cząsteczkowa: 423.42
• UNSPSC Code: 51283505
• NACRES: NA.85
• PubChem Substance ID: 57648295
• EC Number: 214-636-3
• Beilstein/REAXYS Number: 4098179
• MDL number: MFCD00082382

Właściwości

• biological source: synthetic
• Quality Segment: 200
• 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

Opis

General description

Chemical structure: β-lactam

Application

Oxacillin is used to study mechanisms of penicillinase resistance and antimicrobial susceptibility [1]. It has been used to study autolysins[2]

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.

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Informacja o środkach bezpieczeństwa

• Klasa składowania: 11 - Combustible Solids
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)
• pictograms: GHS08
• signalword: Danger
• hcodes: H317,H334
• pcodes: P261 - P272 - P280 - P284 - P302 + P352 - P333 + P313
• Hazard Classifications: Resp. Sens. 1 - Skin Sens. 1