| Description | (-)-Oxypeucedanin hydrate is a furanocoumarin. It has a role as a metabolite. |
| In vitro | Oxypeucedanin exhibited marginal toxicity on normal fibroblast cells and sensitive parental mouse lymphoma cells;?furthermore, they were less toxic on multidrug resistant lymphoma cells.? Oxypeucedanin showed moderate MDR reversing activity.?In the checkerboard assay, oxypeucedanin and heraclenin showed slight synergistic effect with doxorubicin.?These compounds might improve the cytotoxic effect of the standard chemotherapeutic drug doxorubicin. |
| Cell experiments | Pure compounds were isolated from the extract of aerial parts of the plant by chromatographic methods.Bioactivities were tested on multidrug resistant and sensitive mouse T-lymphoma cell lines.The inhibition of the cancer MDR efflux pump ABCB1 was evaluated by flow cytometry (at 2 and 20 μM).A checkerboard microplate method was applied to study the interactions of furocoumarins and doxorubicin.Toxicity was studied using normal murine NIH/3T3 fibroblasts. |
| Synonyms | 水合氧化前胡素, OXYPEUCEDANIN HYDRATE |
| molecular weight | 304.29 |
| Molecular formula | C16H16O6 |
| CAS | 133164-11-1 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
| Solubility | DMSO: 55 mg/mL (180.75 mM) |
| References | 1. Mottaghipisheh J , Márta Nové, Spengler G , et al. Antiproliferative and cytotoxic activities of furocoumarins of Ducrosia anethifolia[J]. Pharmaceutical Biology, 2018, 56(1):658-664. |