A7926

Azlocillin sodium salt

• Synonym(s): D-α-([Imidazolidin-2-on-1-yl]carbonylamino)benzylpenicillin
• Linear Formula: C₂₀H₂₂N₅O₆SNa
• CAS Number: 37091-65-9
• Molecular Weight: 483.47
• NACRES: NA.85
• PubChem Substance ID: 24891295
• UNSPSC Code: 51282412
• EC Number: 253-347-7
• MDL number: MFCD07793330

Properties

• form: powder
• antibiotic activity spectrum: Gram-negative bacteria, Gram-positive bacteria
• mode of action: cell wall synthesis | interferes
• storage temp.: room temp
• SMILES string: [Na+].CC1(C)SC2[C@H](NC(=O)[C@H](NC(=O)N3CCNC3=O)c4ccccc4)C(=O)N2[C@H]1C([O-])=O
• InChI: 1S/C20H23N5O6S.Na/c1-20(2)13(17(28)29)25-15(27)12(16(25)32-20)22-14(26)11(10-6-4-3-5-7-10)23-19(31)24-9-8-21-18(24)30;/h3-7,11-13,16H,8-9H2,1-2H3,(H,21,30)(H,22,26)(H,23,31)(H,28,29);/q;+1/p-1/t11-,12-,13+,16-;/m1./s1
• InChI key: UVOCNBWUHNCKJM-XFAPPKAWSA-M

Description

General description

Chemical structure: β-lactam

Application

Azlocillin is often used against <l>Pseudomonas aeruginosa </l>and has been used to develop novel antibiotic quantitation techniques [1].

Biochem/physiol Actions

Azlocillin is a semisynthetic penicillin and a β-lactam antibiotic. It acts by inhibition of penicillin-binding protein (PBP)-dependent bacterial cell wall synthesis.

Other Notes

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

Safety Information

• pictograms: GHS08
• signalword: Danger
• hcodes: H317,H334
• pcodes: P280 - P302 + P352
• Hazard Classifications: Resp. Sens. 1 - Skin Sens. 1
• Storage Class: 13 - Non Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Faceshields, Gloves