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Mepixanox | CAS No: 17854-59-0 | GMP-certified suppliers

A medication that serves as a respiratory system agent candidate within the xanthene class, intended for investigational use in respiratory disorder research and pharmaceutical development.

Therapeutic categories

Heterocyclic Compounds, Fused-RingRespiratory System AgentsXanthenes
Generic name
Mepixanox
Molecule type
small molecule
CAS number
17854-59-0
DrugBank ID
DB13579
Approval status
Experimental drug
ATC code
R07AB09

Product Snapshot

  • Mepixanox is formulated as an oral solution or drops
  • It is indicated for experimental therapeutic applications
  • The compound currently holds an experimental approval status with no established regulatory authorizations

Clinical Overview

Mepixanox (CAS Number 17854-59-0) is a chemical entity classified within the xanthone family, characterized by a polycyclic aromatic structure incorporating a xanthene moiety conjugated to a ketone functional group at carbon 9. Xanthones are tricyclic compounds composed of two benzene rings fused through a central pyran ring. This structural class is notable for diverse biological activities, although specific details on Mepixanox’s pharmacological profile remain incomplete.

Currently, Mepixanox is designated as an experimental compound and has not received formal approval for therapeutic use. It is categorized under respiratory system agents, suggesting potential investigational application in respiratory disorders, though no explicit clinical indications or pharmacodynamics data have been reported. The absence of mechanistic information limits understanding of its mode of action.

No detailed absorption, distribution, metabolism, and excretion (ADME) parameters are available for Mepixanox. Likewise, comprehensive safety, toxicity, or tolerability data have not been disclosed in public scientific literature. Such data would be essential for evaluating its risk-benefit profile and informing clinical development.

Due to the lack of branded formulations and regulatory approval, Mepixanox is primarily of interest in research and early-phase pharmaceutical investigation rather than routine clinical use. Its categorization as a fused-ring heterocyclic compound with potential respiratory system activity may guide further studies.

When considering Mepixanox for API procurement, emphasis should be placed on sourcing from manufacturers that adhere to stringent quality standards, including compliance with good manufacturing practice (GMP) and thorough impurity profiling. The experimental status of the compound necessitates careful verification of batch consistency and analytical characterization to support research and development activities.

Identification & chemistry

Generic name Mepixanox
Molecule type Small molecule
CAS 17854-59-0
UNII 7419T4YQQW
DrugBank ID DB13579

Formulation & handling

  • Mepixanox is formulated for oral administration, commonly as a solution or drops.
  • As a small molecule with moderate lipophilicity (LogP 3.59) and low water solubility, solubilization strategies may be required for formulation.
  • No specific data indicates sensitivity to food or metabolic instability; however, its polycyclic aromatic structure warrants consideration of photostability and oxidation during handling.

Regulatory status

Mepixanox is a type of Respiratory Tract Agents


Respiratory Tract Agents are a vital category of pharmaceutical APIs (Active Pharmaceutical Ingredients) designed to treat respiratory conditions and diseases. These agents are specifically formulated to target the respiratory system, which includes the lungs, airways, and nasal passages. They play a crucial role in managing various respiratory disorders, such as asthma, chronic obstructive pulmonary disease (COPD), and allergic rhinitis.

Respiratory Tract Agents encompass a wide range of medications, including bronchodilators, corticosteroids, antihistamines, and mucolytics. Bronchodilators are commonly used to relieve airway constriction and facilitate smooth breathing by relaxing the muscles in the airways. Corticosteroids help reduce inflammation in the respiratory system, alleviating symptoms and preventing exacerbations. Antihistamines work by blocking histamine receptors, thus mitigating allergic reactions that often impact the respiratory tract. Mucolytics aid in loosening and thinning mucus, making it easier to expel from the airways.

These APIs are developed through rigorous research and development processes, ensuring their efficacy, safety, and compliance with regulatory standards. Pharmaceutical manufacturers rely on advanced technologies and stringent quality control measures to produce high-quality Respiratory Tract Agents. These APIs are subsequently incorporated into various dosage forms, including inhalers, nasal sprays, nebulizers, and oral medications.

Respiratory Tract Agents are essential in the management of respiratory conditions, providing relief from symptoms, improving lung function, and enhancing the overall quality of life for patients. They are prescribed by healthcare professionals and often used in combination therapies to achieve optimal results. As respiratory disorders continue to affect a significant portion of the global population, the development and availability of effective Respiratory Tract Agents play a vital role in addressing these health challenges and improving patient outcomes.