Lunasin (lunasin) vs Ammonaps (sodium phenylbutyrate)

Lunasin (lunasin) vs Ammonaps (sodium phenylbutyrate)

Lunasin is a peptide initially identified in soybeans that has been researched for its potential health benefits, including anti-inflammatory and anticancer properties, although its efficacy and applications in clinical settings remain under investigation. Ammonaps, also known as sodium phenylbutyrate, is a medication approved for the treatment of urea cycle disorders, which are genetic conditions that affect the body's ability to remove ammonia from the bloodstream. When deciding between Lunasin and Ammonaps, it is crucial to consider the specific medical condition being treated, as Ammonaps is an established treatment for a specific medical indication, while Lunasin's use in clinical settings is not yet well-defined and should be discussed with a healthcare provider.

Difference between Lunasin and Ammonaps

Metric Lunasin (lunasin) Ammonaps (sodium phenylbutyrate)
Generic name Lunasin Sodium phenylbutyrate
Indications Not specified; under investigation for various potential uses Urea cycle disorders
Mechanism of action Believed to have anti-inflammatory and anticancer properties Converts to phenylacetate which reacts with glutamine to form phenylacetylglutamine, thereby reducing ammonia levels
Brand names Not available as a prescription drug under a brand name Buphenyl, Pheburane
Administrative route Oral (as part of dietary supplements) Oral, Rectal
Side effects Limited data available Body odor, taste aversion, nausea, headache, fatigue, rash
Contraindications Limited data available Hypersensitivity to sodium phenylbutyrate or its excipients, hepatic or renal impairment
Drug class Not classified as a drug Urea cycle disorder agent
Manufacturer Not applicable Horizon Pharma (Buphenyl), Swedish Orphan Biovitrum (Pheburane)

Efficacy

Lunasin and Amyotrophic Lateral Sclerosis (ALS)

Lunasin is a peptide originally identified in soybeans, and it has been studied for its potential health benefits, including anti-inflammatory and neuroprotective effects. In the context of Amyotrophic Lateral Sclerosis (ALS), a progressive neurodegenerative disease, Lunasin has attracted interest due to its potential to modulate pathways that could be involved in the disease's progression. However, the efficacy of Lunasin in treating or altering the course of ALS has not been conclusively demonstrated in large-scale clinical trials. Early studies and anecdotal reports have suggested possible benefits, but these findings require validation through more rigorous scientific investigation.

Ammonaps (Sodium Phenylbutyrate) and ALS

Ammonaps, known generically as sodium phenylbutyrate, is a drug approved for the treatment of urea cycle disorders, which are genetic disorders that lead to the accumulation of ammonia in the blood. Its efficacy in ALS has been explored due to its potential to reduce neuronal stress and modulate gene expression. Research into sodium phenylbutyrate for ALS has indicated that it may have neuroprotective effects and could potentially improve certain cellular functions that are compromised in ALS. Nonetheless, the clinical impact of sodium phenylbutyrate on ALS progression and patient outcomes remains to be fully established through controlled clinical trials.

Combined Therapy Approach

Some research has investigated the combined use of Lunasin and sodium phenylbutyrate in ALS. The rationale behind this combination therapy is that each compound might target different aspects of the disease, potentially leading to a more effective treatment strategy. While preclinical studies have shown promise, the translation of these findings to clinical efficacy in ALS patients requires further investigation. It is critical that any combined therapy approach be supported by evidence from clinical trials that assess not only efficacy but also safety and tolerability in the ALS population.

Current Status of Research

As of the current knowledge cutoff, the research into Lunasin and sodium phenylbutyrate for the treatment of ALS is ongoing. While there is some preliminary evidence that suggests potential benefits, the medical community awaits more definitive results from well-designed clinical trials. Patients with ALS and healthcare providers are encouraged to discuss the risks and benefits of any new or off-label treatments and to consider participation in clinical trials as a means to contribute to the advancement of knowledge in this challenging disease area.

Regulatory Agency Approvals

Lunasin
  • Food and Drug Administration (FDA), USA
Ammonaps
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia

Access Lunasin or Ammonaps today

If Lunasin or Ammonaps are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

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