Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Methyllycaconitine analogues have mixed antagonist effects at nicotinic acetylcholine receptors

Loading...
Thumbnail Image

Date

Authors

Barker, David
Lin, Diana S-H
Carland, Jane E
Chu, Cindy P-Y
Chebib, Mary
Brimble, Margaret A
Savage, G Paul
McLeod, Malcolm

Journal Title

Journal ISSN

Volume Title

Publisher

Pergamon-Elsevier Ltd

Abstract

Bicyclic analogues of methyllycaconitine (MLA), such as 12, have been synthesised that incorporate the C1-OMe substituent present in the natural product. Electrophysiology experiments using Xenopus oocytes expressing nicotinic acetylcholine receptors (nAChRs) were conducted on these analogues and a related tricyclic analogue 2. The most potent compound, 2, was an antagonist at all receptors studied but displayed different antagonist effects at each receptor subtype. This study more clearly defines the biological effects of MLA analogues at nAChRs and demonstrates that these analogues are not selective ligands for the α7 nAChR subtype.

Description

Citation

Source

Bioorganic and Medicinal Chemistry

Book Title

Entity type

Access Statement

License Rights

Restricted until

2037-12-31
abcd