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Tuaimenal A, a Meroterpene from the Irish Deep-Sea Soft Coral Duva florida, Displays Inhibition of the SARS-CoV-2 3CLpro Enzyme

[Image: see text] Cold water benthic environments are a prolific source of structurally diverse molecules with a range of bioactivities against human disease. Specimens of a previously chemically unexplored soft coral, Duva florida, were collected during a deep-sea cruise that sampled marine inverte...

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Detalles Bibliográficos
Autores principales: Avalon, Nicole E., Nafie, Jordan, De Marco Verissimo, Carolina, Warrensford, Luke C., Dietrick, Sarah G., Pittman, Amanda R., Young, Ryan M., Kearns, Fiona L., Smalley, Tracess, Binning, Jennifer M., Dalton, John P., Johnson, Mark P., Woodcock, H. Lee, Allcock, A. Louise, Baker, Bill J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9127705/
https://www.ncbi.nlm.nih.gov/pubmed/35549259
http://dx.doi.org/10.1021/acs.jnatprod.2c00054
Descripción
Sumario:[Image: see text] Cold water benthic environments are a prolific source of structurally diverse molecules with a range of bioactivities against human disease. Specimens of a previously chemically unexplored soft coral, Duva florida, were collected during a deep-sea cruise that sampled marine invertebrates along the Irish continental margin in 2018. Tuaimenal A (1), a cyclized merosesquiterpenoid representing a new carbon scaffold with a highly substituted chromene core, was discovered through exploration of the soft coral secondary metabolome via NMR-guided fractionation. The absolute configuration was determined through vibrational circular dichroism. Functional biochemical assays and in silico docking experiments found tuaimenal A selectively inhibits the viral main protease (3CLpro) of SARS-CoV-2.