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- W2425791736 abstract "Twenty six 7-hydroxylisoflavones, including four new compounds 3r, 3s, 3u and 3v, were successfully synthesized. Among which twenty four, 3a similar to 3x, were directly given by One-Pot strategy from polyphenolic compounds and substituted phenylacetic acids. 2'-Hydroxylisoflavones 4a and 4b were further developed from 2'-methoxylisoflvones 3d and 3g by demethylation. Nine out of twenty-six synthesized compounds exhibited higher selectivity for estrogen receptor ER beta than genistein; 7,8-dihydroxylisoflavones showed better binding affinities for ER P than 7-hydroxylisoflavones; 4'-substituents of isoflavones influenced relative binding affinities (RBA) of ER beta/ER alpha in the order: H>Cl>F>OH; 2', 3' and 5'-substituents reduced the binding affinity to both ER alpha and ER beta." @default.
- W2425791736 created "2016-06-24" @default.
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- W2425791736 date "2011-01-01" @default.
- W2425791736 modified "2023-10-14" @default.
- W2425791736 title "Synthesis and Selective Estrogen Receptor Binding Affinity of 7-Hydroxylisoflavones" @default.
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