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Orthosteric and allosteric potentiation of heteromeric neuronal nicotinic acetylcholine receptors
Heteromeric nicotinic ACh receptors (nAChRs) were thought to have two orthodox agonist‐binding sites at two α/β subunit interfaces. Highly selective ligands are hard to develop by targeting orthodox agonist sites because of high sequence similarity of this binding pocket among different subunits. Re...
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| 出版年: | Br J Pharmacol |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5980197/ https://ncbi.nlm.nih.gov/pubmed/28199738 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.13745 |
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