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Ceftobiprole medocaril
CAS No. 376653-43-9
Ceftobiprole medocaril ( BAL5788 )
Catalog No. M28301 CAS No. 376653-43-9
Ceftobiprole medocaril is the parenteral prodrug of Ceftobiprole. Ceftobiprole is a broad-spectrum cephalosporin with activity against Methicillin-resistant staphylococcus aureus (MRSA).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 393 | Get Quote |
|
| 10MG | 581 | Get Quote |
|
| 25MG | 888 | Get Quote |
|
| 50MG | 1242 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameCeftobiprole medocaril
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NoteResearch use only, not for human use.
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Brief DescriptionCeftobiprole medocaril is the parenteral prodrug of Ceftobiprole. Ceftobiprole is a broad-spectrum cephalosporin with activity against Methicillin-resistant staphylococcus aureus (MRSA).
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DescriptionCeftobiprole medocaril is the parenteral prodrug of Ceftobiprole. Ceftobiprole is a broad-spectrum cephalosporin with activity against Methicillin-resistant staphylococcus aureus (MRSA).(In Vivo):Ceftobiprole medocaril (10, 40, 160 mg/kg; single dose; sc) has T 1/2 s 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 C max /dose values decreases from 1.08 to 0.90 in neutropenic thigh-infected mice .
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SynonymsBAL5788
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PathwayGPCR/G Protein
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TargetAntibacterial
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number376653-43-9
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Formula Weight690.7
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Molecular FormulaC26H26N8O11S2
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(O1)=C(COC(N(CC2)C[C@@H]2N(CC/C2=C\C(CS[C@@H]3[C@@H]4NC(/C(/c5nsc(N)n5)=N\O)=O)=C(C(O)=O)N3C4=O)C2=O)=O)OC1=O
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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.Vo TN, et al. Lignans and triterpenes from the root of Pseuderanthemum carruthersii var. atropurpureum. Chem Pharm Bull (Tokyo). 2012;60(9):1125-33.
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