ent-Atisane Diterpenoids from Euphorbia helioscopia and Their Anti-inflammatory Activities.

Phytochemical investigation on the anti-inflammatory fraction extracted from the whole plant of Euphorbia helioscopia L. led to the isolation of three new ent-atisane diterpenoids (1-3) and five known analogues (4-8). The structures and absolute configurations of the new compounds were elucidated by comprehensive analysis of the NMR, MS, IR, ECD, and X-ray crystallography. It is worth mentioning that compound 3 belongs to a rare class of ent-atisane diterpenoid featuring a hydroxyl group at C-9. Bioactivity investigation showed that compounds 4, 7, and 8 exhibited significant inhibitory effects on LPS-induced NO production in a dose-dependent manner, which indicates their anti-inflammatory potential.

Two New Eremophilane-Type Sesquiterpenoids from Ligularia sagitta.

Two new eremophilane-type sesquiterpenoids, sagittacins F and G (1 and 2), together with one known isomer of sagittacin F (3) were isolated from the leaves and stems of Ligularia sagitta. Their structures were elucidated by interpretation of spectroscopic data and the absolute configurations of 1 and 3 were determined by X-ray spectroscopy. Compound 1 belongs to a rare class of eremophilane-type sesquiterpenoid featuring an α-oriented hydroxy group at C-1. A nitric oxide (NO) production inhibitory assay was applied to evaluate their anti-inflammatory activities by using LPS-induced RAW 264.7 cells. Compounds 2 and 3 exhibited modest NO production inhibitions with IC50 values of 45.15±2.72 and 49.83±2.34 µM, respectively.

N,P-Doped carbon with encapsulated Co nanoparticles as efficient electrocatalysts for oxygen reduction reactions.

Exploring efficient non-noble ORR catalysts as alternatives to Pt-based catalysts are highly demanded for their possible application in fuel cells and rechargeable metal-air batteries. Herein, we demonstrate a rational design and synthesis of a N, P-doped carbon with encapsulated Co nanoparticles as efficient electrocatalysts for ORR. The catalyst is derived from a mixture of Co-MOF and triphenylphosphine with a mass ratio of 3 : 1 by pyrolysis in N2 atmosphere at 700 °C. The catalyst exhibited a superior ORR catalytic performance among its counterparts in 0.1 M KOH with onset and half-wave potentials of 0.88 V and 0.80 V, a much larger limiting current density of -5.93 mA cm-2 that surpassed commercial 20% Pt/C, in addition to its durability and resistance to methanol. This enhanced ORR activity of the catalyst can be attributed to the synergistic effect between Co NPs and N, P atoms, the relatively large contact surface, more exposed active sites and good electrical conductivity. This study would provide some new ideas for the design and construction of promising carbon-based non-precious metal electrocatalysts for future practical fuel cell applications.