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.
Authors
- Yi‐Lin He (ORCID: https://orcid.org/0009-0004-6494-3486)
- Kun Gao
- Guoli Li (ORCID: https://orcid.org/0009-0002-7660-6386)
- Na Gao (ORCID: https://orcid.org/0000-0002-8622-9273)
- Hong‐Ying Yang (ORCID: https://orcid.org/0009-0004-9113-473X)
Institutions
- Lanzhou Jiaotong University (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- Chirality
- Published
- 2025-11-24
- DOI
- https://doi.org/10.1002/chir.70061
- Primary Topic
- Bioactive Natural Diterpenoids Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00