A pair of new isoquinoline alkaloid enantiomers with cardioprotective effect from Corydalis yanhusuo

A new isoquinoline alkaloid derivative, yanhusanine M (1), featuring a rare C-8 hydroxymethyl substituent, was isolated from the tubers of Corydalis yanhusuo. The structure was elucidated by comprehensive spectroscopic analyses, including HR-ESI-MS, IR, 1D and 2D NMR (COSY, HMBC, HSQC, NOESY) and 13C NMR chemical shifts calculations coupled with the DP4+ probability method. It was resolved into its enantiomers, (+)-1 and (−)-1, via chiral-phase HPLC, and their absolute configurations were determined by comparison of experimental and calculated ECD spectra. Both enantiomers exhibited significant cardioprotective effects at the concentrations of 10–500 nM.

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Publication Details

Journal
Journal of Asian Natural Products Research
Published
2026-10-27
DOI
https://doi.org/10.1080/10286020.2026.2748977
Primary Topic
Synthesis and Biological Activity
Type
article
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article

A pair of new isoquinoline alkaloid enantiomers with cardioprotective effect from Corydalis yanhusuo

J Zhou, Huan Xia, Dong-Jie Fang, Gui‐Yang Xia et al.
Journal of Asian Natural Products Research
Synthesis and Biological Activity
article

A pair of new isoquinoline alkaloid enantiomers with cardioprotective effect from Corydalis yanhusuo

J Zhou, Huan Xia, Dong-Jie Fang, Gui‐Yang Xia, Sheng Lin, Xiao-Hong Wei
article en

Abstract

A new isoquinoline alkaloid derivative, yanhusanine M (1), featuring a rare C-8 hydroxymethyl substituent, was isolated from the tubers of Corydalis yanhusuo. The structure was elucidated by comprehensive spectroscopic analyses, including HR-ESI-MS, IR, 1D and 2D NMR (COSY, HMBC, HSQC, NOESY) and 13C NMR chemical shifts calculations coupled with the DP4+ probability method. It was resolved into its enantiomers, (+)-1 and (−)-1, via chiral-phase HPLC, and their absolute configurations were determined by comparison of experimental and calculated ECD spectra. Both enantiomers exhibited significant cardioprotective effects at the concentrations of 10–500 nM.

Journal of Asian Natural Products Research
Qinghai University (CN), Beijing University of Chinese Medicine (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine (CN)
Openalex Percentile: Top 16%
Synthesis and Biological Activity
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