The RCE used in this study was an autohydrolyzed hydroalcoholic extract of the aerial parts of Trifolium pratense L., Fabaceae, which had previously been used in a clinical trial.25 The extract contained 30% w/w isoflavones [BA (14.47%), FN (14.26%), GN (0.41%), and DZ (0.23%)] and was manufactured by Pure World Botanicals, Inc. (South Hackensack, NJ) as described previously.25,27 The chemical profile of this clinical red clover extract, batch BC190, which has been used throughout these studies, was extensively described previously.35 All pure compounds were obtained from Sigma-Aldrich (St. Louis, MO), unless otherwise indicated.
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