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Cefoselis sulfate

Base Information Edit
  • Chemical Name:Cefoselis sulfate
  • CAS No.:122841-12-7
  • Molecular Formula:C19H24N8O10S3
  • Molecular Weight:620.64
  • Hs Code.:
  • UNII:6EY42207VS
  • Mol file:122841-12-7.mol
Cefoselis sulfate

Synonyms:cefoselis;FK 037;FK-037;FK037

Suppliers and Price of Cefoselis sulfate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Medical Isotopes, Inc.
  • CefoselissulfateA
  • 5 mg
  • $ 950.00
  • DC Chemicals
  • Cefoselissulfate >99%
  • 100 mg
  • $ 250.00
  • DC Chemicals
  • Cefoselissulfate >99%
  • 250 mg
  • $ 500.00
  • Crysdot
  • Cefoselissulfate 98+%
  • 100mg
  • $ 352.00
  • ChemScene
  • Cefoselis(sulfate) 99.41%
  • 50mg
  • $ 260.00
  • ChemScene
  • Cefoselis(sulfate) 99.41%
  • 100mg
  • $ 440.00
  • ChemScene
  • Cefoselis(sulfate) 99.41%
  • 5mg
  • $ 60.00
  • ChemScene
  • Cefoselis(sulfate) 99.41%
  • 10mg
  • $ 90.00
  • Chemenu
  • Cefoselissulfate 98%
  • 100mg
  • $ 620.00
  • Biosynth Carbosynth
  • Cefoselis sulfate
  • 10 mg
  • $ 168.80
Total 67 raw suppliers
Chemical Property of Cefoselis sulfate Edit
Chemical Property:
  • Boiling Point:965.8 °C at 760 mmHg 
  • Flash Point:537.9 °C 
  • PSA:337.67000 
  • LogP:0.02710 
  • Hydrogen Bond Donor Count:7
  • Hydrogen Bond Acceptor Count:17
  • Rotatable Bond Count:9
  • Exact Mass:620.07775251
  • Heavy Atom Count:40
  • Complexity:1100
Purity/Quality:

99% *data from raw suppliers

CefoselissulfateA *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CON=C(C1=CSC(=N1)N)C(=O)NC2C3N(C2=O)C(=C(CS3)CN4C=CC(=N)N4CCO)C(=O)O.OS(=O)(=O)O
  • Isomeric SMILES:CO/N=C(/C1=CSC(=N1)N)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)CN4C=CC(=N)N4CCO)C(=O)O.OS(=O)(=O)O
  • Description Cefoselis is a new fourth-generation cephalosporin and was launched in Japan as a parenteral antibiotic for a variety of infections including Staphylococcus aureus (particularly the methicillin-resistant MRSA) and Pseudornonas aeruginosa. It can be prepared in 3 related ways, all using 2- pyrazolomethyl-3-cephem-4-carboxylic as the key intermediate. In preclinical studies, Cefolesis had better MIC50s than Ceftazidime against Streptococcus pneurnoniae or Staphflococcus aureus (methicillin-sensitive MSSA or resistant MRSA) and showed significant antibacterial activity against Citrobacter and Enterobacter. Cefolesis is well tolerated in clinical studies, being eliminated mainly via glomerular filtration in humans.
  • Uses antibiotic
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