Synthesis, Activity, and Application of Fluorescent Analogs of [D1G, Δ14Q]LvIC Targeting α6β4 Nicotinic Acetylcholine Receptor
Author:
Affiliation:
1. Guangxi Key Laboratory of Special Biomedicine; School of Medicine, Guangxi University, Nanning 530004, China
2. Key Laboratory of Tropical Biological Resources of Ministry of Education, Hainan University, Haikou 570228, China
Funder
National Key Research and Development Program of China
Specific Research Project of Guangxi for Research Bases and Talents
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.3c00283
Reference43 articles.
1. Ion channels gated by acetylcholine and serotonin: structures, biology, and drug discovery
2. The nicotinic α6 subunit gene determines variability in chronic pain sensitivity via cross-inhibition of P2X2/3 receptors
3. Nicotinic acetylcholine receptors containing the α6 subunit contribute to ethanol activation of ventral tegmental area dopaminergic neurons
4. Functional Nicotinic Acetylcholine Receptors Containing 6 Subunits Are on GABAergic Neuronal Boutons Adherent to Ventral Tegmental Area Dopamine Neurons
5. Role of α6 nicotinic receptors in CNS dopaminergic function: relevance to addiction and neurological disorders
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