Anti‐Inflammatory Jatrophane Diterpenoids With Multiple Chiral Carbon Centers From <scp> <i>Jatropha curcas</i> </scp>

Two previously undescribed jatrophane-type diterpenoids (1, 2) and 11 known compounds (3-13) were isolated from the whole plants of Jatropha curcas L. Their structures were elucidated using IR, HR-ESI-MS, 1D-, and 2D-NMR spectra, and the absolute configurations were established by ECD. The anti-inflammatory activity of these compounds was evaluated by inhibiting NO production in LPS-stimulated RAW264.7 macrophages, and compounds 5, 8-11, and 13 showed potent activity with IC<sub>50</sub> values ranging from 16.86 to 32.49 μM, which were comparable with that of the positive control l-NMMA (IC<sub>50</sub>: 21.90 μM). The structure-activity relationships of jatrophane-type diterpenoids revealed that compounds 5 and 11 showed the most potent anti-inflammatory effects.

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Publication Details

Journal
Chirality
Published
2025-11-24
DOI
https://doi.org/10.1002/chir.70061
Primary Topic
Bioactive Natural Diterpenoids Research
Type
article
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0.00
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article

Anti‐Inflammatory Jatrophane Diterpenoids With Multiple Chiral Carbon Centers From Jatropha curcas

Yi‐Lin He, Kun Gao, Guoli Li, Na Gao et al.
Chirality
Bioactive Natural Diterpenoids Research
article

Anti‐Inflammatory Jatrophane Diterpenoids With Multiple Chiral Carbon Centers From Jatropha curcas

Yi‐Lin He, Kun Gao, Guoli Li, Na Gao, Hong‐Ying Yang
article en

Abstract

Two previously undescribed jatrophane-type diterpenoids (1, 2) and 11 known compounds (3-13) were isolated from the whole plants of Jatropha curcas L. Their structures were elucidated using IR, HR-ESI-MS, 1D-, and 2D-NMR spectra, and the absolute configurations were established by ECD. The anti-inflammatory activity of these compounds was evaluated by inhibiting NO production in LPS-stimulated RAW264.7 macrophages, and compounds 5, 8-11, and 13 showed potent activity with IC<sub>50</sub> values ranging from 16.86 to 32.49 μM, which were comparable with that of the positive control l-NMMA (IC<sub>50</sub>: 21.90 μM). The structure-activity relationships of jatrophane-type diterpenoids revealed that compounds 5 and 11 showed the most potent anti-inflammatory effects.

ChiralityVol. 37(12)
Lanzhou Jiaotong University (CN), Lanzhou University (CN)
Openalex Percentile: Top 67%
Bioactive Natural Diterpenoids Research
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Anti‐Inflammatory Jatrophane Diterpenoids With Multiple Chiral Carbon Centers From <scp> <i>Jatropha curcas</i> </scp> — Yi‐Lin He, Kun Gao, et al. · Chirality (2025) | TGRS Research Map | TGRS