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- W2131955620 abstract "The highly potent natural alkaloid epibatidine remains a source of inspiration in the search for new analgesic drugs. In this paper, we describe an expansion of our previously reported synthesis of epibatidine analogues, and five synthetic alkaloids characterized by a symmetric, 1-substituted 7-azabicyclo[2.2.1]heptane skeleton, were evaluated for their biological activity. Two of these are binding selectively to the α4β2 subtype of the nicotinic acetylcholine receptor. Their Ki values were determined to be 40 and 290 nM. After a favourable evaluation of these compounds' cytotoxicity and metabolic stability, they were submitted to a rat tail flick test. The compounds did not show antinociceptive effects, which may be caused by a combination of insufficient potency and poor brain penetration." @default.
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- W2131955620 date "2014-01-01" @default.
- W2131955620 modified "2023-10-03" @default.
- W2131955620 title "Synthesis of 1-substituted epibatidine analogues and their in vitro and in vivo evaluation as α4β2nicotinic acetylcholine receptor ligands" @default.
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- W2131955620 doi "https://doi.org/10.1039/c3ra44379e" @default.
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