4-Oxystilbene compounds are selective ligands for neuronal nicotinic αBungarotoxin receptors

1. Starting from the structure of an old 4-oxystilbene derivate with ganglioplegic activity (MG624), we synthesized two further derivates (F2 and F3) and two stereoisomers of F3 (F3A and F3B), and studied their selective effect on neuronal nicotinic acetylcholine receptor (AChR) subtypes. 2. MG 624,...

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Bibliografiset tiedot
Päätekijät: Gotti, C, Balestra, B, Moretti, M, Rovati, G E, Maggi, L, Rossoni, G, Berti, F, Villa, L, Pallavicini, M, Clementi, F
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1998
Aiheet:
Papers
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1565512/
https://ncbi.nlm.nih.gov/pubmed/9720791
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.bjp.0701957
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