CAS 42540-40-9: Cefamandole nafate
Formula:C19H18N6O6S2·Na
InChI:InChI=1S/C19H18N6O6S2.Na/c1-24-19(21-22-23-24)33-8-11-7-32-17-12(16(28)25(17)13(11)18(29)30)20-15(27)14(31-9-26)10-5-3-2-4-6-10;/h2-6,9,12,14,17H,7-8H2,1H3,(H,20,27)(H,29,30);/t12-,14-,17-;/m1./s1
InChI key:InChIKey=FUWWBXJEMYXCMO-YCLOEFEOSA-N
SMILES:C(O)(=O)C=1N2[C@@]([C@H](NC([C@H](OC=O)C3=CC=CC=C3)=O)C2=O)(SCC1CSC=4N(C)N=NN4)[H].[Na]
Synonyms:- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2R)-(formyloxy)phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, (6R,7R)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2R)-2-(formyloxy)-2-phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, sodium salt (1:1), (6R,7R)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(formyloxy)phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, [6R-[6α,7β(R*)]]-
- Bergacef
- Cedol
- Cefam
- Cefamandole Nafate
- Cefamandole formate sodium
- Cefiran
- Cemado
- Cemandil
- See more synonyms
Sort by
Found 8 products.
CEFAMANDOLE NAFATE CRS
CAS:CEFAMANDOLE NAFATE CRSFormula:C19H17N6NaO6S2Color and Shape:White. Powder.Molecular weight:512.4946Sodium (6R,7R)-7-(R)-mandelamido-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate formate (ester)
CAS:Formula:C19H17N6NaO6S2Purity:98%Color and Shape:SolidMolecular weight:512.4946Cefamandole nafate
CAS:Formula:C19H17N6O6S2NaColor and Shape:White to off-white powderMolecular weight:512.49Cefamandole Nafate
CAS:Controlled ProductApplications Antibacterial. References Taha, M., et al.: Bioorg. Med. Chem., 16, 1218 (2008), Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010),Formula:C19H17N6O6S2·NaColor and Shape:NeatMolecular weight:512.49Cefamandole nafate
CAS:Cefamandole nafate is an antimicrobial agent that is used for the treatment of infectious diseases. It has a broad spectrum of activity and is effective against Gram-positive and Gram-negative bacteria, such as staphylococci, streptococci, and pseudomonads. Cefamandole nafate has been shown to be active against tissue infection caused by E. coli in rats. The mechanism of action involves cell lysis and the formation of sodium carbonate. This reaction takes place when glucose is injected into the animal's intrauterine cavity before injecting cefamandole nafate solution. The chemical reaction between sodium carbonate and glucose produces water, carbon dioxide, sodium bicarbonate, and hydrogen ions. The hydrogen ions react with cefamandole to produce its active form, which then reacts with the bacterial cell wall by disrupting the cell membrane. Cefamandole nafate also inhibits protein synthesis by bindingFormula:C19H17N6NaO6S2Purity:Min. 95%Molecular weight:512.5 g/molCefamandole Nafate (DISCONTINUED)
CAS:Antibiotics nesoiFormula:C19H18N6O6S2·NaColor and Shape:Crystalline SolidMolecular weight:513.06269Cefamandole nafate
CAS:Cefamandole nafate (Cephamandole nafate) is a second-generation broad-spectrum cephalosporin antibiotic.Formula:C19H17N6NaO6S2Purity:97.47%Color and Shape:White SolidMolecular weight:512.49
![Sodium (6R,7R)-7-(R)-mandelamido-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabic…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2FIN%2Fthumb%2FDA00I88D.jpg&w=3840&q=75)
