Chalcone-Monoterpene Derivatives from the Buds of and Their Potential as Protein Tyrosine Phosphatase 1B Inhibitors.

Four new compounds, racemic chalcone-monoterpene hybrids (-) and a chalcone (), along with nine known compounds (-, -), have been isolated from the buds of . The chemical structures of the isolated compounds were identified through NMR data analysis and confirmed by computational methods, including electronic circular dichroism (ECD) calculations, and further synthetic approaches. Compounds - were synthesized via a Diels-Alder reaction, a process informed by biomimetic condensation studies that combined chalcones and monoterpenes. These synthetic approaches also yielded various unnatural chalcone-monoterpene derivatives (-). The inhibitory effects on protein tyrosine phosphatase 1B (PTP1B) of both naturally isolated and synthetically obtained compounds were evaluated. Compounds , , , and exhibited potent PTP1B inhibitory activity, with IC values ranging from 0.9 ± 0.2 to 3.9 ± 0.7 μM. The enantiomers (+)- and (-)- showed enhanced activity compared to their respective enantiomers. Kinetic studies indicate that all active compounds inhibit PTP1B through mixed mechanisms, and molecular docking simulations agree with the experimental assays on PTP1B. Our results suggest that chalcone-meroterpene adducts from the buds of exhibit potential as antidiabetic agents, partly due to their PTP1B enzyme inhibition.