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Diterpenoids with anti-inflammatory activities from Isodon rubescens
Xia Tang1, Jin-Lu Xu2, Xin-Yue Li2
1Guangdong Provincial Key Laboratory of Translational Cancer Research of Chinese Medicines, Joint International Research Laboratory of Translational Cancer Research of Chinese Medicines, International Institute for Translational Chinese Medicine, School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou 510006, China; Chinese Medicine Guangdong Laboratory (Hengqin Laboratory), Guangdong-Macao In-Depth Cooperation Zone in Hengqin, Hengqin 519000, China.
Nine new diterpenoids from Isodon rubescens were identified. Compound 10 demonstrated significant anti-inflammatory activity by inhibiting NF-κB nuclear translocation without cytotoxicity.
Area of Science:
- Natural Products Chemistry
- Pharmacology
Background:
- Isodon rubescens is a plant source of bioactive compounds.
- Diterpenoids are a class of natural products with diverse biological activities.
Purpose of the Study:
- To isolate and characterize new diterpenoids from Isodon rubescens.
- To evaluate the anti-inflammatory potential of isolated compounds.
Main Methods:
- Isolation of compounds using chromatographic techniques.
- Structure elucidation via mass spectrometry and X-ray crystallography.
- In vitro anti-inflammatory assay using lipopolysaccharide-stimulated RAW264.7 cells.
Main Results:
- Nine new diterpenoids (Henanabinins A-I) and 14 known analogues were isolated.
- Structures of new compounds were determined, with compound 1's absolute configuration confirmed by X-ray diffraction.
- Compound 10 (rubescensin B) showed potent inhibition of NF-κB nuclear translocation (IC50 = 3.073 μM) and no cytotoxicity at 12.5 μM.
Conclusions:
- Isodon rubescens is a rich source of structurally diverse diterpenoids.
- Rubescensin B exhibits promising anti-inflammatory properties via NF-κB inhibition.
- Further investigation into rubescensin B as a potential anti-inflammatory agent is warranted.
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