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Pharmacological activity of C10-substituted analogs of the high-affinity kainate receptor agonist dysiherbaine
Kainate receptor antagonists have potential as therapeutic agents in a number of neuropathologies. Synthetic modification of the convulsant marine toxin neodysiherbaine A (NDH) previously yielded molecules with a diverse set of pharmacological actions on kainate receptors. Here we characterize three...
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| Main Authors: | , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2009
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2813386/ https://ncbi.nlm.nih.gov/pubmed/19962997 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuropharm.2009.11.013 |
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