Two new cassane diterpenoids from the seed kernels of <i>Caesalpinia sinensis</i>

Two new cassane diterpenoids, sucupiranin MN (<b>1</b>) and sucupiranin ML (<b>2</b>), together with two known compounds sucutinirane C (<b>3</b>) and deacetylsucutinirane C (<b>4</b>) were isolated from the seed kernels of <i>Caesalpinia sinensis</i>. Their structures were elucidated by means of analysis of comprehensive spectroscopic data, especially HRESIMS and 1D/2D NMR spectroscopy. Compounds <b>1–4</b> are typical furan-type cassane derivatives with an aromatized C ring. Biological evaluation revealed that compounds <b>1–4</b> at the concentration of 10 μM could inhibit the overproduction of NO in LPS-stimulated RAW 264.7 macrophages.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.25325034
Primary Topic
Biological Stains and Phytochemicals
Type
article
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article

Two new cassane diterpenoids from the seed kernels of Caesalpinia sinensis

Figshare
Biological Stains and Phytochemicals
article

Two new cassane diterpenoids from the seed kernels of Caesalpinia sinensis

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Abstract

Two new cassane diterpenoids, sucupiranin MN (<b>1</b>) and sucupiranin ML (<b>2</b>), together with two known compounds sucutinirane C (<b>3</b>) and deacetylsucutinirane C (<b>4</b>) were isolated from the seed kernels of <i>Caesalpinia sinensis</i>. Their structures were elucidated by means of analysis of comprehensive spectroscopic data, especially HRESIMS and 1D/2D NMR spectroscopy. Compounds <b>1–4</b> are typical furan-type cassane derivatives with an aromatized C ring. Biological evaluation revealed that compounds <b>1–4</b> at the concentration of 10 μM could inhibit the overproduction of NO in LPS-stimulated RAW 264.7 macrophages.

Figshare
Openalex Percentile: Top 44%
Biological Stains and Phytochemicals
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Two new cassane diterpenoids from the seed kernels of <i>Caesalpinia sinensis</i> · Figshare (2025) | TGRS Research Map | TGRS