Chemical Name:N-[2-(5-Hydroxy-1H-indol-3-yl)ethyl]-2-oxo-3-piperidinecarboxamide
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Selective TrkB receptor agonist. Protects neurons from excitotoxicity. Protects retinas from light-induced retinal degeneration (LIRD) in vivo. Blood brain barrier and blood-retinal barrier penetrant.
Technical Data
M. Wt
301.34
Formula
C16H19N3O3
Storage
Store at -20°C
Purity
≥98% (HPLC)
CAS Number
314054-36-9
PubChem ID
5012758
InChI Key
ZIMKJLALTRLXJO-UHFFFAOYSA-N
Smiles
OC1=CC=C2NC=C(C2=C1)CCNC(C3CCCNC3=O)=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
DMSO
30.13
100
Preparing Stock Solutions
The following data is based on the product molecular weight 301.34. 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
3.32 mL
16.59 mL
33.19 mL
5 mM
0.66 mL
3.32 mL
6.64 mL
10 mM
0.33 mL
1.66 mL
3.32 mL
50 mM
0.07 mL
0.33 mL
0.66 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.
Setterholmet al (2015) Gram-scale, chemoselective synthesis of N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-2-oxopiperidine-3-carboxamide (HIOC) Tetrahedron Lett. 56 3413 PMID: 26028783
Shenet al (2012) N-acetyl serotonin derivatives as potent neuroprotectants for retinas Proc.Natl.Acad.Sci.USA 109 3540 PMID: 22331903