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Oxeladin | CAS No: 468-61-1 | GMP-certified suppliers
A medication that was historically used as a central nervous system antitussive agent for cough suppression but is now obsolete due to safety and regulatory concerns.
Therapeutic categories
Acids, CarbocyclicAntitussive AgentsCentral Nervous System AgentsCough and Cold PreparationsRespiratory System Agents
Generic name
Oxeladin
Molecule type
small molecule
CAS number
468-61-1
DrugBank ID
DB04822
Approval status
Approved drug, Withdrawn drug
ATC code
R05DB09
Product Snapshot
- Oxeladin is available as oral solutions, tablets, and syrups, representing non-injectable small molecule formulations
- It is primarily utilized for respiratory indications requiring cough suppression
- The product has a mixed regulatory status with approvals in some markets and withdrawals in others
Clinical Overview
Oxeladin (CAS Number 468-61-1) is an organic compound classified within the phenylpropane chemical class, characterized by the presence of a phenylpropane moiety. It has historically been utilized as an antitussive agent, acting on the central nervous system to suppress cough. Despite its previous medical use in cough and cold preparations and respiratory system treatments, oxeladin's clinical indication is not specifically defined in available data.
Pharmacodynamic and detailed mechanism of action information for oxeladin is not available in the literature. As an antitussive, it was presumably intended to modulate the cough reflex centrally, although precise receptor targets or pathways have not been documented.
The compound was withdrawn from the Canadian, United States, and United Kingdom markets in 1976 due to its association with carcinogenicity. Toxicological studies identified risks that outweighed therapeutic benefits, leading to its market removal. Due to this history, oxeladin is no longer approved for clinical use and carries significant safety concerns.
Key absorption, distribution, metabolism, and excretion (ADME) parameters have not been published or are inaccessible. Given its withdrawal and lack of contemporary data, current pharmaceutical use is effectively obsolete.
Oxeladin was historically marketed under various formulations as a cough suppressant but no notable brands remain active in current pharmaceutical channels. Regulatory oversight prohibits its clinical use in countries with stringent safety standards.
For formulation scientists and API sourcing professionals, strict due diligence is essential when handling oxeladin. Its carcinogenic potential mandates comprehensive quality control and compliance with hazardous substance regulations. Sourcing of oxeladin APIs should consider its regulatory status, potential legal constraints, and the necessity of validated purity and impurity profiles to ensure worker safety and environmental containment.
Pharmacodynamic and detailed mechanism of action information for oxeladin is not available in the literature. As an antitussive, it was presumably intended to modulate the cough reflex centrally, although precise receptor targets or pathways have not been documented.
The compound was withdrawn from the Canadian, United States, and United Kingdom markets in 1976 due to its association with carcinogenicity. Toxicological studies identified risks that outweighed therapeutic benefits, leading to its market removal. Due to this history, oxeladin is no longer approved for clinical use and carries significant safety concerns.
Key absorption, distribution, metabolism, and excretion (ADME) parameters have not been published or are inaccessible. Given its withdrawal and lack of contemporary data, current pharmaceutical use is effectively obsolete.
Oxeladin was historically marketed under various formulations as a cough suppressant but no notable brands remain active in current pharmaceutical channels. Regulatory oversight prohibits its clinical use in countries with stringent safety standards.
For formulation scientists and API sourcing professionals, strict due diligence is essential when handling oxeladin. Its carcinogenic potential mandates comprehensive quality control and compliance with hazardous substance regulations. Sourcing of oxeladin APIs should consider its regulatory status, potential legal constraints, and the necessity of validated purity and impurity profiles to ensure worker safety and environmental containment.
Identification & chemistry
| Generic name | Oxeladin |
|---|---|
| Molecule type | Small molecule |
| CAS | 468-61-1 |
| UNII | SNC1080T5Y |
| DrugBank ID | DB04822 |
Formulation & handling
- Oxeladin is a small molecule with low water solubility, primarily formulated for oral administration in solutions, tablets, and syrups.
- Given its high LogP of 4.43, solubility enhancement strategies may be needed for bioavailability improvement in formulations.
- No peptide or biologic considerations apply; stability and handling should consider potential sensitivity to moisture and light due to its phenylpropane structure.
