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Submit ReviewTrofinetide is an IGF-1 synthetic analog. It suppresses expression of IL-1β, TNF-α, IFN-γ and E-selectin, and inhibits both acute and delayed neuroinflammation following penetrating ballistic-like brain injury (PBBI) in rats.
M. Wt | 315.32 |
Formula | C13H21N3O6 |
Storage | Store at -20°C |
Purity | ≥98% (HPLC) |
CAS Number | 853400-76-7 |
InChI Key | BUSXWGRAOZQTEY-SDBXPKJASA-N |
Smiles | C(N[C@@H](CCC(O)=O)C(O)=O)(=O)[C@@]1(C)N(C(CN)=O)CCC1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
water | 31.53 | 100 | |
DMSO | 15.77 | 50 with gentle warming |
The following data is based on the product molecular weight 315.32. Batch specific molecular weights may vary from batch to batch due to the degree 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 | 3.17 mL | 15.86 mL | 31.71 mL |
5 mM | 0.63 mL | 3.17 mL | 6.34 mL |
10 mM | 0.32 mL | 1.59 mL | 3.17 mL |
50 mM | 0.06 mL | 0.32 mL | 0.63 mL |
References are publications that support the biological activity of the product.
Wei et al (2009) NNZ-2566 treatment inhibits neuroinflammation and pro-inflammatory cytokine expression induced by experimental penetrating ballistic-like brain injury in rats. J.Neuroinflammation 6 19 PMID: 19656406
If you know of a relevant reference for Trofinetide, please let us know.
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Citations are publications that use Tocris products.
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Written by Sonia Tucci, Lynsay Kobelis and Tim Kirkham, this review provides a synopsis of the increasing number of peptides that have been implicated in appetite regulation and energy homeostasis; putative roles of the major peptides are outlined and compounds available from Tocris are listed.