Cefamandole nafate
CAS No. 42540-40-9
Cefamandole nafate( Cephamandole nafate | Cefamandole formate sodium )
Catalog No. M19801 CAS No. 42540-40-9
Cefamandole nafate is a second-generation broad-spectrum cephalosporin antibiotic.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 31 | In Stock |
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| 100MG | 44 | In Stock |
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| 200MG | 60 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCefamandole nafate
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NoteResearch use only, not for human use.
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Brief DescriptionCefamandole nafate is a second-generation broad-spectrum cephalosporin antibiotic.
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DescriptionCefamandole nafate is a second-generation broad-spectrum cephalosporin antibiotic.(In Vitro):Cefamandole nafate is shown to be rapidly converted to cefamandole in bacteriological media, with a half-life of less than 1 h at a pH of 7.0 or above. At pH 6.0, in log-phase inhibition experiments, however, Cefamandole nafate is more stable, allowing delineation of the activity between cefamandole and cefamandole nafate.(In Vivo):The toxicity of Cefamandole nafate administered iv Is studied in rats receiving doses of 250-1,000 mg/kgfive days per week for one month.After the administration of Cefamandole nafate for one month, there are no treatment-related adverse effects on growth, food consumption, clinical chemistry, hematology, or organ weights.
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In VitroCefamandole nafate is shown to be rapidly converted to cefamandole in bacteriological media, with a half-life of less than 1 h at a pH of 7.0 or above. At pH 6.0, in log-phase inhibition experiments, however, Cefamandole nafate is more stable, allowing delineation of the activity between cefamandole and cefamandole nafate.
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In VivoThe toxicity of Cefamandole nafate administered iv Is studied in rats receiving doses of 250-1,000 mg/kg five days per week for one month.After the administration of Cefamandole nafate for one month, there are no treatment-related adverse effects on growth, food consumption, clinical chemistry, hematology, or organ weights.
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SynonymsCephamandole nafate | Cefamandole formate sodium
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorBacterial
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Research AreaInflammation/Immunology
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IndicationPulmonary infection urinary tract infection biliary tract infection skin and soft tissue infection bone and joint infection
Chemical Information
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CAS Number42540-40-9
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Formula Weight512.49
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Molecular FormulaC19H17N6NaO6S2
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 41 mg/mL (80.00 mM);Water:≥ 29 mg/mL (56.59 mM)
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SMILES[Na+].Cn1nnnc1SCC1=C(N2[C@H](SC1)[C@H](NC(=O)[C@H](OC=O)c1ccccc1)C2=O)C([O-])=O
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Chemical Namesodium;(6R7R)-7-[[(2R)-2-formyloxy-2-phenylacetyl]amino]-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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MAC13772
MAC13772 is a potent inhibitor of BioA with an IC50 of 250 nM, a novel antibacterial inhibitor that selectively inhibits PABA biosynthesis in M tuberculosis.
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Calcimycin
Calcimycin is an ionophorous, polyether carboxylic antibiotic from Streptomyces chartreusensis.?It binds and transports calcium and other divalent cations across membranes and uncouples oxidative phosphorylation while inhibiting ATPase of rat liver mitochondria.?The substance is used mostly as a biochemical tool to study the role of divalent cations in various biological systems.?
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Azidamfenicol
Azidamfenicol inhibits ribosomal peptidyltransferase with a Ki of 22 μM. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.
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