Chemical Name:N,N',N''Tris(2-hydroxyethyl)-1,3,5-benzenetricarboxamide
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Potent tropomyosin-related kinase B (TrkB) agonist (IC50 = 47 nM). Induces activation of Trk, Akt and ERK in mouse hippocampus and striatum. Reverses deficits in motor task learning in mice following traumatic brain injury; restores respiratory function in a rat model of Rett syndrome.
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Technical Data
M. Wt
339.34
Formula
C15H21N3O6
Storage
Store at +4°C
Purity
≥98% (HPLC)
CAS Number
37988-18-4
PubChem ID
2054170
InChI Key
RGWJKANXFYJKHN-UHFFFAOYSA-N
Smiles
O=C(NCCO)C1=CC(C(NCCO)=O)=CC(C(NCCO)=O)=C1
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
DMSO
33.93
100
water
33.93
100
Preparing Stock Solutions
The following data is based on the product molecular weight 339.34. 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
2.95 mL
14.73 mL
29.47 mL
5 mM
0.59 mL
2.95 mL
5.89 mL
10 mM
0.29 mL
1.47 mL
2.95 mL
50 mM
0.06 mL
0.29 mL
0.59 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Massaet al (2010) Small molecule BDNF mimetics activate TrkB signaling and prevent neuronal degeneration in rodents. J.Clin.Invest. 120 1774 PMID: 20407211
Schmidet al (2012) A TrkB small molecule partial agonist rescues TrkB phosphorylation deficits and improves respiratory function in a mouse model of Rett syndrome. J.Neurosci. 32 1803 PMID: 22302819