| Literature DB >> 33502811 |
Fabien Emmetiere1, Ranjala Ratnayake2, Henry A M Schares3, Katherine F M Jones4, Emily Bevan-Smith1, Hendrik Luesch2, Daniel A Harki3,4, Alexander J Grenning1.
Abstract
Described herein is a function-oriented synthesis route and biological evaluation of pseudoguaianolide analogues. The 10-step synthetic route developed retains the topological complexity of the natural product, installs functional handles for late-stage diversification, and forges the key bioactive Michael acceptors early in the synthesis. The analogues were found to be low-micromolar Nrf2 activators and micromolar NF-κB inhibitors and dependent on the local environment of the Michael acceptor moieties.Entities:
Keywords: NF-κB inhibitors; Nrf2 activators; enyne metathesis; modular synthesis; pseudoguaianolides
Mesh:
Substances:
Year: 2021 PMID: 33502811 PMCID: PMC8195264 DOI: 10.1002/chem.202100038
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236