4.7 Article

Diversity-oriented synthesis of diterpenoid alkaloids yields a potent anti-inflammatory agent

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PHYTOMEDICINE
卷 117, 期 -, 页码 -

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ELSEVIER GMBH
DOI: 10.1016/j.phymed.2023.154907

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Natural products; Diterpenoid alkaloids; Diversity-oriented synthesis; Anti-inflammatory; Autophagy

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A series of new derivatives were synthesized from the diterpenoid alkaloids deltaline and talatisamine through a diversity-oriented synthesis strategy. These derivatives demonstrated strong anti-inflammatory effects and were able to suppress the secretion of inflammatory factors. The representative derivative deltanaline showed potent anti-inflammatory activity in both in vitro and in vivo models, making it a promising lead compound for the treatment of inflammatory diseases.
Background: The diterpenoid alkaloids belong to a highly esteemed group of natural compounds, which display significant biological activities. It is a productive strategy to expand the chemical space of these intriguing natural compounds for drug discovery. Methods: We prepared a series of new derivatives bearing diverse skeletons and functionalities from the diterpenoid alkaloids deltaline and talatisamine based on a diversity-oriented synthesis strategy. The antiinflammatory activity of these derivatives was initially screened and evaluated by the release of nitric oxide (NO), tumor necrosis factor (TNF-alpha), and interleukin-6 (IL-6) in lipopolysaccharide (LPS)-activated RAW264.7 cells. Futhermore, the anti-inflammatory activity of the representative derivative 31a was validated in various inflammatory animal models, including phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced mice ear edema, LPS-stimulated acute kidney injury, and collagen-induced arthritis (CIA). Results: It was found that several derivatives were able to suppress the secretion of NO, TNF-alpha, and IL-6 in LPSactivated RAW264.7 cells. Compound 31a, one of the representative derivatives named as deltanaline, demonstrated the strongest anti-inflammatory effects in LPS-activated macrophages and three different animal models of inflammatory diseases by inhibiting nuclear factor kappa-B (NF-kappa B)/mitogen-activated protein kinase (MAPK) signaling and inducing autophagy. Conclusion: Deltanaline is a new structural compound derived from natural diterpenoid alkaloids, which may serve as a new lead compound for the treatment of inflammatory diseases.

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