Amide-Iminoate Isomerism in Antineuroinflammatory Isoquinoline Alkaloids from .

J Nat Prod

State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Guangxi Normal University, Guilin 541004, People's Republic of China.

Published: April 2020

Six new (-) and two known (, ) alkaloids that were chemically inseparable geometrical isomers (two isomers present in a 1:1 ratio for - and and a 1:3 ratio for , , and ) were identified from . Their structures and absolute configurations were determined by spectroscopic data analyses and comparison of their experimental and calculated ECD spectra. Moreover, using NOE correlations and DFT-based calculations, the NMR data of each geometrical isomer of - were assigned. The biological evaluation of - showed that and have stronger inhibitory effects (IC values, 12.0 and 12.6 μM, respectively) than minocycline (IC value, 17.5 μM) against NO production in overactivated BV2 cells, suggesting they have great potential in the development of neuroinflammatory therapeutics for treating neurodegenerative diseases.

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http://dx.doi.org/10.1021/acs.jnatprod.9b00483DOI Listing

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Amide-Iminoate Isomerism in Antineuroinflammatory Isoquinoline Alkaloids from .

J Nat Prod

April 2020

State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, Guangxi Normal University, Guilin 541004, People's Republic of China.

Six new (-) and two known (, ) alkaloids that were chemically inseparable geometrical isomers (two isomers present in a 1:1 ratio for - and and a 1:3 ratio for , , and ) were identified from . Their structures and absolute configurations were determined by spectroscopic data analyses and comparison of their experimental and calculated ECD spectra. Moreover, using NOE correlations and DFT-based calculations, the NMR data of each geometrical isomer of - were assigned.

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