Weight | 279.344 g/mol |
---|---|
Formula | C13H21N5O2 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 3 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
Tezampanel (154652-83-2)
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SMILESC1CC2CNC(CC2CC1CCC3=NNN=N3)C(=O)O
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InChIKeyZXFRFPSZAKNPQQ-UHFFFAOYSA-N
- Pubchem - Tezampanel
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Tezampanel (INN, USAN) (code names LY-293,558, NGX-424) is a drug originally developed by Eli Lilly which acts as a competitive antagonist of the AMPA and kainate subtypes of the ionotropic glutamate receptor family, with selectivity for the GluR5 subtype of the kainate receptor. It has neuroprotective and anticonvulsant properties, the former of which may, at least in part, occur via blockade of calcium uptake into neurons. Tezampanel has a range of effects which may be useful for medicinal purposes, as well as its applications in scientific research.
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