Cefotaxime sodium
CAS No. 64485-93-4
Cefotaxime sodium( —— )
Catalog No. M15447 CAS No. 64485-93-4
Cefotaxime is a third-generation cephalosporin antibiotic. Like other third-generation cephalosporins, it has broad spectrum activity against Gram positive and Gram negative bacteria.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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500MG | 102 | In Stock |
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Biological Information
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Product NameCefotaxime sodium
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NoteResearch use only, not for human use.
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Brief DescriptionCefotaxime is a third-generation cephalosporin antibiotic. Like other third-generation cephalosporins, it has broad spectrum activity against Gram positive and Gram negative bacteria.
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DescriptionCefotaxime is a third-generation cephalosporin antibiotic. Like other third-generation cephalosporins, it has broad spectrum activity against Gram positive and Gram negative bacteria. In most cases, it is considered to be equivalent to ceftriaxone in terms of safety and efficacy. Cefotaxime sodium is marketed under various trade names including Claforan (Sanofi-Aventis). (In Vitro):Cefotaxime sodium exhibits an MIC of 0.0625 mg/L for V. vulnificus CMCP6.(In Vivo):The combination of ciprofloxacin and cefotaxime is more effective in clearing V. vulnificus in vivo than previously used regimens.
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In VitroCefotaxime sodium exhibits an MIC of 0.0625 mg/L for V. vulnificus CMCP6.
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In VivoThe combination of ciprofloxacin and cefotaxime is more effective in clearing V. vulnificus in vivo than previously used regimens. Animal Model:Female, specific pathogen free, 8-week-old BALB/c mice.Dosage:30 mg/kg.Administration:IP every 6 h.Result:The viable bacterial counts in liver were lower in mice treated with cefotaxime-plus-ciprofloxacin than in those treated with cefotaxime alone (P<0.001 at 24 h and 48 h, each).
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Synonyms——
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorPBPs
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Research AreaInfection
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Indication——
Chemical Information
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CAS Number64485-93-4
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Formula Weight477.44
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Molecular FormulaC16H16N5NaO7S2
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Purity>98% (HPLC)
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SolubilityDMSO: 47mg/mL
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SMILESCC(=O)OCC1=C(N2[C@@H]([C@@H](C2=O)NC(=O)/C(=N\OC)/C3=CSC(=N3)N)SC1)C(=O)[O-].[Na+]
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Williamson R, et al. Antimicrob Agents ChemOthers. 1980 Oct;18(4):629-37.
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