Two new steroidal alkaloids from the aerial part of <i>Fritillaria walujewii</i>

Phytochemical investigation on the aerial part of <i>Fritillaria walujewii</i> Regel resulted in the isolation of two new steroidal alkaloids, named as walujewine F (<b>1</b>) and G (<b>2</b>), and five previously reported compounds <b>3</b>-<b>7</b>. Structural elucidation of compounds <b>1</b>-<b>7</b> was achieved by employing various spectroscopic techniques. The cholinesterase inhibitory potential of all the compounds was systematically evaluated. Compound <b>1</b> exhibited moderate AChE inhibition with the IC<sub>50</sub> value of 70.37 μM, while compound <b>2</b> demonstrated obvious dual AChE and BChE inhibitory effects, with the IC<sub>50</sub> values of 91.69 μM and 67.12 μM, respectively, but lower than the positive control galantamine (IC<sub>50</sub> values of 2.80 μM for AChE and 21.85 μM for BChE).

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Publication Details

Journal
Natural Product Research
Published
2025-12-17
DOI
https://doi.org/10.1080/14786419.2025.2605668
Primary Topic
Phytochemical Studies and Bioactivities
Type
article
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article

Two new steroidal alkaloids from the aerial part of Fritillaria walujewii

Tong Sun, Yu‐Ming Liu, Wenkai Zhao, Lei Yingjie et al.
Natural Product Research
Phytochemical Studies and Bioactivities
article

Two new steroidal alkaloids from the aerial part of Fritillaria walujewii

Tong Sun, Yu‐Ming Liu, Wenkai Zhao, Lei Yingjie, Feng-Chen Wu
article en

Abstract

Phytochemical investigation on the aerial part of <i>Fritillaria walujewii</i> Regel resulted in the isolation of two new steroidal alkaloids, named as walujewine F (<b>1</b>) and G (<b>2</b>), and five previously reported compounds <b>3</b>-<b>7</b>. Structural elucidation of compounds <b>1</b>-<b>7</b> was achieved by employing various spectroscopic techniques. The cholinesterase inhibitory potential of all the compounds was systematically evaluated. Compound <b>1</b> exhibited moderate AChE inhibition with the IC<sub>50</sub> value of 70.37 μM, while compound <b>2</b> demonstrated obvious dual AChE and BChE inhibitory effects, with the IC<sub>50</sub> values of 91.69 μM and 67.12 μM, respectively, but lower than the positive control galantamine (IC<sub>50</sub> values of 2.80 μM for AChE and 21.85 μM for BChE).

Natural Product Research
Tianjin University of Science and Technology (CN), Tianjin University of Technology and Education (CN), Tianjin University of Technology (CN), Tianjin Institute of Pharmaceutical Research (China) (CN)
Openalex Percentile: Top 63%
Phytochemical Studies and Bioactivities
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Two new steroidal alkaloids from the aerial part of <i>Fritillaria walujewii</i> — Tong Sun, Yu‐Ming Liu, et al. · Natural Product Research (2025) | TGRS Research Map | TGRS