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Novel mechanism of modulation at a ligand‐gated ion channel; action of 5‐Cl‐indole at the 5‐HT(3)A receptor
BACKGROUND AND PURPOSE: The 5‐HT(3) receptor is a prototypical member of the Cys‐loop ligand‐gated ion channel (LGIC) superfamily and an established therapeutic target. In addition to activation via the orthosteric site, receptor function can be modulated by allosteric ligands. We have investigated...
Uloženo v:
| Vydáno v: | Br J Pharmacol |
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| Hlavní autoři: | , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5120152/ https://ncbi.nlm.nih.gov/pubmed/27677804 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.13638 |
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