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Bisoxatin acetate | CAS No: 14008-48-1 | GMP-certified suppliers
A medication that is currently experimental, intended for research in medicinal chemistry with potential applications in various disease areas pending clinical investigation.
Generic name
Bisoxatin acetate
Molecule type
small molecule
CAS number
14008-48-1
DrugBank ID
DB14654
Approval status
Experimental drug
Product Snapshot
- Bisoxatin acetate is an oral small molecule formulation
- It is primarily developed for experimental use in metabolic and inflammatory conditions
- The compound is currently in the experimental stage with no approved regulatory status
Clinical Overview
Bisoxatin acetate (CAS number 14008-48-1) is an organic compound classified within the diphenylmethane chemical class. Diphenylmethanes are characterized by a central methane moiety bonded to two phenyl groups, conferring a distinct structural framework often relevant in medicinal chemistry.
This compound is currently designated as experimental, with no approved clinical indications or established therapeutic uses. Consequently, details regarding its pharmacodynamics, mechanism of action, or drug category classification remain unavailable in the public domain. Similarly, clinically relevant pharmacological profiles such as target receptors, enzyme interactions, or modulation pathways have not been characterized to date.
Pharmacokinetic information including absorption, distribution, metabolism, and excretion (ADME) parameters has not been reported. Without these data, the systemic exposure, bioavailability, metabolic stability, and clearance mechanisms are unknown. Safety and toxicity profiles have not been documented, limiting assessment of its tolerability or potential adverse effects in humans.
No marketed formulations or brand names correspond to Bisoxatin acetate currently. Its usage context remains restricted to research and experimental studies, highlighting its early developmental status in pharmaceutical pipelines.
From a sourcing perspective, procurement of Bisoxatin acetate API should focus on suppliers adhering to stringent quality control standards. Due to its experimental nature, ensuring chemical purity, batch-to-batch consistency, and compliance with regulatory guidelines for research-grade materials is critical. Verification via analytical methods such as NMR, HPLC, and mass spectrometry is recommended to confirm identity and specification adherence. Additionally, comprehensive documentation regarding manufacturing processes and impurity profiles will facilitate regulatory submissions and investigational use.
This compound is currently designated as experimental, with no approved clinical indications or established therapeutic uses. Consequently, details regarding its pharmacodynamics, mechanism of action, or drug category classification remain unavailable in the public domain. Similarly, clinically relevant pharmacological profiles such as target receptors, enzyme interactions, or modulation pathways have not been characterized to date.
Pharmacokinetic information including absorption, distribution, metabolism, and excretion (ADME) parameters has not been reported. Without these data, the systemic exposure, bioavailability, metabolic stability, and clearance mechanisms are unknown. Safety and toxicity profiles have not been documented, limiting assessment of its tolerability or potential adverse effects in humans.
No marketed formulations or brand names correspond to Bisoxatin acetate currently. Its usage context remains restricted to research and experimental studies, highlighting its early developmental status in pharmaceutical pipelines.
From a sourcing perspective, procurement of Bisoxatin acetate API should focus on suppliers adhering to stringent quality control standards. Due to its experimental nature, ensuring chemical purity, batch-to-batch consistency, and compliance with regulatory guidelines for research-grade materials is critical. Verification via analytical methods such as NMR, HPLC, and mass spectrometry is recommended to confirm identity and specification adherence. Additionally, comprehensive documentation regarding manufacturing processes and impurity profiles will facilitate regulatory submissions and investigational use.
Identification & chemistry
| Generic name | Bisoxatin acetate |
|---|---|
| Molecule type | Small molecule |
| CAS | 14008-48-1 |
| UNII | 79W5LFS83K |
| DrugBank ID | DB14654 |
Formulation & handling
- Bisoxatin acetate is a small molecule with low water solubility, indicating formulation strategies may require solubilizing agents or suitable solvents for oral administration. Its moderate lipophilicity (LogP 3.57) suggests potential for good membrane permeability but limited aqueous solubility. Stability considerations should include protection from moisture due to its low water solubility and experimental status, requiring validation under various storage conditions.
