SML1631

Cefodizime Sodium

≥96% (HPLC)

• Sinónimos: 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(2-amino-4-thiazoly)(methoxyimino)acetyl}-3-[[[5-(carboxymethyl)-4-methyl-2-thiazilyl]-8-oxo-, sodium salt (1:2), (6R,7R)-
• Fórmula empírica (notación de Hill): C₂₀H₁₈N₆O₇S₄ · 2Na
• Número de CAS: 86329-79-5
• Peso molecular: 628.63
• UNSPSC Code: 12352200
• PubChem Substance ID: 329825515

Propiedades

• biological source: synthetic
• assay: ≥96% (HPLC)
• form: powder
• solubility: H₂O: soluble 270 mg/mL
• storage temp.: 2-8°C
• SMILES string: O=C1[C@@H](NC(/C(C2=CSC(N)=N2)=N\OC)=O)[C@]3([H])N1C(C([O-])=O)=C(CSC4=NC(C)=C(CC([O-])=O)S4)CC3
• InChI: 1S/C20H20N6O7S4.2Na/c1-7-10(3-11(27)28)37-20(22-7)36-5-8-4-34-17-13(16(30)26(17)14(8)18(31)32)24-15(29)12(25-33-2)9-6-35-19(21)23-9;;/h6,13,17H,3-5H2,1-2H3,(H2,21,23)(H,24,29)(H,27,28)(H,31,32);;/q;2*+1/p-2/b25-12-;;/t13-,17-;;/m1../s1
• InChI key: WBOBLQIRACJNPA-AEKYOGSZSA-L

Descripción

Biochem/physiol Actions

Cefodizime is a third generation cephalosporin with a broad spectrum of antibacterial activity. Cefodizime was demonstrated to be effective against upper and lower respiratory tract infections, urinary tract infections, and gonorrhea. Cefodizime regulates the cytokines expression of neutrophils through toll-like receptor 4 (TLR-4) stimulated by Klebsiella pneumonie.

Información de seguridad

• pictograms: GHS07
• signalword: Warning
• hcodes: H319
• pcodes: P305 + P351 + P338
• Hazard Classifications: Eye Irrit. 2
• Storage Class: 13 - Non Combustible Solids
• wgk_germany: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable