
Biological Activity
Synthetic thyrotropin-releasing hormone (TRH) analog. Displays ~ 30 - 100-fold more potent CNS activity and ~ 50-fold weaker endocrine activity than TRH. Antinociceptive and neuroprotective.
Technical Data
M. Wt | 405.41 |
Formula | C17H23N7O5 |
Storage | Store at -20°C |
Purity | ≥96% (HPLC) |
CAS Number | 103300-74-9 |
PubChem ID | 114750 |
InChI Key | LQZAIAZUDWIVPM-SRVKXCTJSA-N |
Smiles | CN(C(C[C@@H]([C@@](N[C@@H](CC3=CNC=N3)C(N2[C@H]([C@](N)=O)CCC2)=O)=O)N1)=O)C1=O |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
water | 20.27 | 50 |
Preparing Stock Solutions
The following data is based on the product molecular weight 405.41. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.47 mL | 12.33 mL | 24.67 mL |
5 mM | 0.49 mL | 2.47 mL | 4.93 mL |
10 mM | 0.25 mL | 1.23 mL | 2.47 mL |
50 mM | 0.05 mL | 0.25 mL | 0.49 mL |
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Product Datasheets
References
References are publications that support the products' biological activity.
Suzuki et al (1990) Synthesis and central nervous system actions of thyrotropin-releasing hormone analogues containing a dihydroorotic acid moiety. J.Med.Chem. 33 2130 PMID: 2115588
Urayama et al (2002) Neuroprotective effect and brain receptor binding of taltirelin, a novel thyrotropin-releasing hormone (TRH) analogue, in transient forebrain ischemia of C57BL/6J mice. Life Sci. 72 601 PMID: 12467901
Tanabe et al (2007) The synthetic TRH analogue taltirelin exerts modality-specific antinociceptive effects via distinct descending monoaminergic systems. Br.J.Pharmacol. 150 403 PMID: 17220907
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