Several analogues of 7-O-and 40-O-substituted isoxanthohumol and 8-prenylnaringenin, the strongest known phytoestrogen and potential anticancerogenic agent, were synthesized. Acyl, alkyl, and allyl derivatives of isoxanthohumol underwent the demethylation process using MgI2 × 2Et2O in anhydrous THF with the yields of 61-89%. Some of the compounds approached the international criteria of antiproliferative activity (4μg/ml) for synthetic agents against the human cancer cell lines.
CITATION STYLE
Anioł, M., Świderska, A., Stompor, M., & Żołnierczyk, A. K. (2012). Antiproliferative activity and synthesis of 8-prenylnaringenin derivatives by demethylation of 7-O-and 4’-O-substituted isoxanthohumols. Medicinal Chemistry Research, 21(12), 4230–4238. https://doi.org/10.1007/s00044-011-9967-8
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