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Zabofloxacin

Base Information
  • Chemical Name:Zabofloxacin
  • CAS No.:219680-11-2
  • Molecular Formula:C19H20FN5O4
  • Molecular Weight:401.397
  • Hs Code.:
  • UNII:LV66BA6V2G
  • Wikipedia:Zabofloxacin
  • Wikidata:Q17143544
  • NCI Thesaurus Code:C82232
  • ChEMBL ID:CHEMBL2107811
  • Mol file:219680-11-2.mol
Zabofloxacin

Synonyms:DW-224a;zabofloxacin

Suppliers and Price of Zabofloxacin
Supply Marketing:
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
Total 7 raw suppliers
Chemical Property of Zabofloxacin
Chemical Property:
  • PSA:109.05000 
  • LogP:1.37450 
  • XLogP3:-0.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:4
  • Exact Mass:401.14993230
  • Heavy Atom Count:29
  • Complexity:794
Purity/Quality:

97% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CON=C1CN(CC12CNC2)C3=C(C=C4C(=O)C(=CN(C4=N3)C5CC5)C(=O)O)F
  • Isomeric SMILES:CO/N=C/1\CN(CC12CNC2)C3=C(C=C4C(=O)C(=CN(C4=N3)C5CC5)C(=O)O)F
  • Recent ClinicalTrials:Evaluation of Pharmacokinetics Profiles and Bactericidal Activity of Zabofloxacin
  • Description Zabofloxacin is a quinolone antibiotic originally developed by Dong Wha Pharmaceuticals and licensed to Pacific Beach Biosciences in 2007. In March 2015, Korea’s Ministry of Food and Drug Safety (MFDS) approved zabofloxacin for the treatment of acute bacterial exacerbation of chronic obstructive pulmonary disease (ABE-COPD). In 2016, zabofloxacin gained approval from the USFDA for the treatment of community-acquired pneumonia. ABE-COPD is caused by respiratory tract and pulmonary parenchyma that cause chronic pulmonary inflammation and obstruction in the respiratory tract, which leads to irreversible damage. In the nonclinical evaluation process, zabofloxacin showed strong antibiotic activity on respiratory germs (e.g., Streptococcus pneumonia, S. Haemophilus, S. moraxella) and was the most potent antibacterial agent against penicillin-resistant S. pneumoniae (PRSP) in the murine systemic infection model.
Technology Process of Zabofloxacin

There total 16 articles about Zabofloxacin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 5 steps
1.1: ethanol / 4 h / 75 - 78 °C / Large scale
1.2: 2 h / 20 - 25 °C / Large scale
2.1: sodium hydroxide / ethyl acetate; water / 2 h / 0 - 25 °C
2.2: 4 h / 20 - 30 °C
2.3: 2 h / 20 - 25 °C
3.1: triethylamine / acetonitrile / 5 h / 55 - 60 °C / Large scale
4.1: trifluoroacetic acid / dichloromethane / 5 h / 0 - 20 °C / Large scale
4.2: -15 - -10 °C / Large scale
5.1: ethanol; water / 0.5 h / 20 - 25 °C / Large scale
With triethylamine; trifluoroacetic acid; sodium hydroxide; In ethanol; dichloromethane; water; ethyl acetate; acetonitrile;
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