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Adam W Keasling

2 papers in the library · 2 citations · publishing 2019-2023

Papers

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Heteroaromatic salvinorin A analogue (P-3 l) elicits antinociceptive and anxiolytic-like effects.

Fitoterapia June 1, 2023 Caroline V. L. Moreira, Ana Luiza G Faria, Daiany P B Silva et al. 2 citations

Previous studies have attributed the prominent analgesic, hallucinogenic, sedative, and anxiolytic properties of Salvia divinorum to Salvinorin A. However, the overall pharmacological profile of this isolate limits its clinical applications. To address these limitations, our study evaluates the C(22)-fused-heteroaromatic analogue of salvinorin A [2-O-salvinorin B benzofuran-2-carboxylate]...

DOI: 10.1016/j.fitote.2023.105488 (opens in new tab) Full text (opens in new tab) Antinociceptive Anxiolytic Benzodiazepine site Opioid receptors +14

Salvindolin elicits opioid system-mediated antinociceptive and antidepressant-like activities.

Journal of Psychopharmacology July 2019 Adam W Keasling, Pankaj Pandey, Robert J Doerksen et al.

Salvinorin A is known as a highly selective kappa opioid receptor agonist with antinociceptive but mostly pro-depressive effects. In this article, we present its new semisynthetic analog with preferential mu opioid affinity, and promising antinociceptive, as well as antidepressant-like activities. Competitive binding studies were performed for salvindolin with kappa opioid and mu opioid. The...