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Danofloxacin API Manufacturers & Suppliers

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Danofloxacin | CAS No: 112398-08-0 | GMP-certified suppliers

A medication that treats bacterial infections in animals by providing broad-spectrum anti-infective activity for effective veterinary use.

Therapeutic categories

Anti-Infective AgentsHeterocyclic Compounds, Fused-RingQuinolinesQuinolones
Generic name
Danofloxacin
Molecule type
small molecule
CAS number
112398-08-0
DrugBank ID
DB11393
Approval status
Experimental drug, Vet_approved drug

Product Snapshot

  • Danofloxacin is an injectable small molecule formulated for intramuscular administration
  • The compound is primarily used in veterinary applications for bacterial infections
  • It holds experimental status in human use and is approved for veterinary use

Clinical Overview

Danofloxacin is a fluoroquinolone antibiotic primarily utilized in veterinary medicine. It belongs to the chemical class of quinoline carboxylic acids, characterized by a quinoline ring structure substituted with at least one carboxyl group. The compound functions as an anti-infective agent targeting bacterial pathogens in animals.

Although specific clinical indications for danofloxacin are not detailed here, fluoroquinolones are generally employed for treating bacterial infections in a variety of animal species. Danofloxacin is approved for veterinary use in certain regions and is categorized as an experimental or veterinary-approved agent depending on local regulatory frameworks.

The pharmacological action of danofloxacin is consistent with others in the fluoroquinolone class. These agents exert bactericidal effects by inhibiting bacterial DNA gyrase and topoisomerase IV enzymes. This inhibition disrupts critical processes of DNA replication, transcription, and repair, ultimately leading to bacterial cell death. The drug is active against a broad spectrum of gram-negative and some gram-positive bacteria, although specific susceptibility profiles may vary by pathogen and animal species.

Key absorption, distribution, metabolism, and excretion (ADME) properties of danofloxacin have been studied in target animals, demonstrating adequate systemic bioavailability following oral or parenteral administration. The compound is known to achieve effective tissue penetration, supporting its use in systemic infections. Metabolism is limited, with primary elimination occurring via renal excretion of unchanged drug.

From a safety standpoint, fluoroquinolones, including danofloxacin, may carry risks of adverse effects such as cartilage development inhibition in juvenile animals, central nervous system disturbances, and potential for resistance development with improper use. Veterinary formulations undergo safety assessments appropriate to intended species.

Notable brand names for danofloxacin formulations vary by market. Due to the specificity of veterinary usage, product availability is typically controlled to ensure proper prescribing and administration.

When sourcing danofloxacin API, it is critical to verify compliance with veterinary pharmaceutical standards, including purity, residual solvent limits, and absence of contaminants. Procurement from manufacturers adhering to Good Manufacturing Practices (GMP) and holding relevant regulatory certifications ensures API quality suitable for incorporation into veterinary medicinal products.

Identification & chemistry

Generic name Danofloxacin
Molecule type Small molecule
CAS 112398-08-0
UNII 24CU1YS91D
DrugBank ID DB11393

Formulation & handling

  • Danofloxacin is a small molecule quinoline carboxylic acid primarily formulated for intramuscular injection in veterinary use.
  • Moderate water solubility (0.738 g/L) supports parenteral formulation but requires control of pH and excipients for stability.
  • Not a peptide or biologic, thus less sensitive to proteolytic degradation but formulation should consider chemical stability and potential photodegradation.

Regulatory status

Danofloxacin is a type of Antibacterials


Antibacterials, a category of pharmaceutical active pharmaceutical ingredients (APIs), play a crucial role in combating bacterial infections. These APIs are chemical compounds that target and inhibit the growth or kill bacteria, helping to eliminate harmful bacterial pathogens from the body.

Antibacterials are essential for the treatment of various bacterial infections, including respiratory tract infections, urinary tract infections, skin and soft tissue infections, and more. They are commonly prescribed by healthcare professionals to combat both mild and severe bacterial infections.

Within the category of antibacterials, there are different classes and subclasses of APIs, each with distinct mechanisms of action and target bacteria. Some commonly used antibacterials include penicillins, cephalosporins, tetracyclines, macrolides, and fluoroquinolones. These APIs work by interfering with various aspects of bacterial cellular processes, such as cell wall synthesis, protein synthesis, DNA replication, or enzyme activity.

The development and production of antibacterial APIs require stringent quality control measures to ensure their safety, efficacy, and purity. Pharmaceutical manufacturers must adhere to Good Manufacturing Practices (GMP) and follow rigorous testing protocols to guarantee the quality and consistency of these APIs.

As bacterial resistance to antibiotics continues to be a significant concern, ongoing research and development efforts aim to discover and develop new antibacterial APIs. The evolution of antibacterials plays a crucial role in combating emerging bacterial strains and ensuring effective treatment options for infectious diseases.

In summary, antibacterials are a vital category of pharmaceutical APIs used to treat bacterial infections. They are designed to inhibit or kill bacteria, and their development requires strict adherence to quality control standards. By continually advancing research in this field, scientists and pharmaceutical companies can contribute to the ongoing battle against bacterial infections.