ChemicalBook--->CAS DataBase List--->252188-71-9

252188-71-9

252188-71-9 Structure

252188-71-9 Structure
IdentificationBack Directory
[Name]

Ceftobiprole Medocaril Sodium Sterile Powder
[CAS]

252188-71-9
[Synonyms]

CEFTOBIPROLE MEDOCARIL SODIUM
Ceftobiprole medocaril sodium
Ceftobiprole Medocaril Sodium Sterile Powder
Sodium (6R,7R)-3-((E)-(1-((R)-1-(((5-methyl-2-oxo-1,3-dioxol-4-yl)methoxy)carbonyl)pyrrolidin-3-yl)-2-oxopyrrolidin-3-ylidene)methyl)-7-((Z)-2-(5-amin
[EINECS(EC#)]

607-653-6
[Molecular Formula]

C26H27N8NaO11S2
[MOL File]

252188-71-9.mol
[Molecular Weight]

714.66
Chemical PropertiesBack Directory
[storage temp. ]

4°C, away from moisture and light
[solubility ]

DMSO : 250 mg/mL (350.81 mM; Need ultrasonic)
[form ]

Solid
[color ]

Off-white to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Danger
[Hazard statements ]

H334-H317
[Precautionary statements ]

P261-P285-P304+P341-P342+P311-P501-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501
Hazard InformationBack Directory
[Uses]

Broad spectrum antibiotic.
[Clinical Use]

#N/A
[in vivo]

Ceftobiprole medocaril (s.c.; 3 × q12h; total daily doses of BAL9141 equivalents, 2.1, 4.2, or 8.4 mg/kg) causes ten-day cumulative survival rates ranged from 57 to 100% for female Swiss albino mice (body weight, 20 to 22 g) infected Penr Cros Ctxs strain P-15986[1].
Ceftobiprole medocaril (10, 40, 160 mg/kg; single dose; sc) has T1/2s from 20 min to 31 min, as the dose rose from 40 mg/kg to 160 mg/kg. The AUC/dose values for the escalating single doses ranges from 0.585 to 1.33, and the Cmax/dose values decreases from 1.08 to 0.90 in neutropenic thigh-infected mice[2].

[Drug interactions]

Potentially hazardous interactions with other drugs
Anticoagulants: effects of coumarins may be enhanced.
[Metabolism]

Ceftobiprole medocaril sodium is the pro-drug of the active moiety ceftobiprole. Conversion from the prodrug ceftobiprole medocaril sodium, to the active moiety ceftobiprole, occurs rapidly and is mediated by non-specific plasma esterases. Ceftobiprole undergoes minimal metabolism to the open-ring metabolite, which is microbiologically inactive
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