Taltirelin
From PeptidePlaza, the free peptide reference · Entry #1125 · Nootropic · Sources fetched 2026-09-11 · Editorial standards
Taltirelin (also known as taltireline, TA 0910, taltirelina, taltirelinum) is a nootropic research peptide. Taltirelin is a synthetic thyrotropin-releasing hormone (TRH) analog that acts as an agonist for the thyrotropin-releasing hormone receptor.
Taltirelin is a thyrotropin-releasing hormone receptor agonist, mimicking the action of natural TRH. It is currently in Phase 2 clinical trials. Research has explored its potential as a respiratory stimulant, particularly with arousal properties, and as a reversal agent for opioid-induced respiratory depression. Studies also investigate its role in inducing tyrosine hydroxylase (TH) expression by regulating TRHR and RAR in medium spiny neurons, and its potential application in the treatment of spinocerebellar degeneration.
1 Mechanism of action
Thyrotropin-releasing hormone receptor agonist (agonist)
Primary targets: Thyrotropin-releasing hormone receptor
2 Chemical and physical properties
| CAS number | 103300-74-9 |
|---|---|
| Molar mass | 405.4 g/mol |
| Purity (typical) | Not independently verified |
| Storage | −20 °C, lyophilised powder, desiccated |
| Solubility | Sterile water / bacteriostatic water |
| Receptors / targets | Thyrotropin-releasing hormone receptor |
3 Research studies (8)
- A method for predicting drugs that can boost the efficacy of immune checkpoint blockade
Nature immunology (2024) - Thyrotropin-releasing hormone analog as a stable upper airway-preferring respiratory stimulant with arousal properties
Journal of applied physiology (Bethesda, Md. : 1985) (2022) - Are thyrotropin-releasing hormone (TRH) and analog taltirelin viable reversal agents of opioid-induced respiratory depression?
Pharmacology research & perspectives (2022) · Review - Taltirelin induces TH expression by regulating TRHR and RARα in medium spiny neurons
Journal of translational medicine (2024) - [Treatment for Spinocerebellar Degeneration]
Brain and nerve = Shinkei kenkyu no shinpo (2023) - A Comparison of Breathing Stimulants for Reversal of Synthetic Opioid-Induced Respiratory Depression in Conscious Rats
The Journal of pharmacology and experimental therapeutics (2021) - Diversity of thyrotropin-releasing hormone receptors in the pituitary and discrete brain regions of rats
Japanese journal of pharmacology (1999) - [Synthesis and pharmacological action of TRH analog peptide (Taltirelin)]
Nihon yakurigaku zasshi. Folia pharmacologica Japonica (1997) · Review
4 Safety and risk profile
4.1 Regulatory status
Taltirelin is currently classified as Phase 2 clinical trials. It has no approved human indication in the United States; availability elsewhere does not imply demonstrated safety or efficacy.
5 Frequently asked questions
- What is taltirelin?
- Taltirelin is a synthetic analog of thyrotropin-releasing hormone (TRH). It functions as an agonist, meaning it activates the thyrotropin-releasing hormone receptor, mimicking the effects of the natural hormone.
- How does taltirelin work?
- Taltirelin works by acting as an agonist for the thyrotropin-releasing hormone receptor. This mechanism allows it to stimulate pathways associated with TRH, including inducing tyrosine hydroxylase expression by regulating TRHR and RAR in specific neurons.
- What is taltirelin studied for?
- Taltirelin is studied for its potential as a respiratory stimulant, particularly for its arousal properties, and as a reversal agent for opioid-induced respiratory depression. It is also investigated for its role in spinocerebellar degeneration and its ability to induce TH expression.
- What is the regulatory status of taltirelin?
- Taltirelin is currently in Phase 2 clinical trials. This indicates that it is undergoing further evaluation for its efficacy and safety in a larger group of people after initial safety assessments.
6 References
- Taltirelin — compound summary PubChem. View source
- Taltirelin — molecule record ChEMBL. View source
- Taltirelin — published literature (65 records) PubMed. View source
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