Er Alpha-Agonist And Er Beta-Antagonist Bifunctional Next-Generation Bisphenols With No Halogens: Bpap, Bpb, And Bpz

As demonstrated for bisphenol AF (BPAF), the electrostatic halogen bond based on the London dispersion force of halogen atoms was found to be a major driving force of their bifunctional ER alpha-agonist and ER beta antagonist activities. Because similar electronic effects are anticipated for hydrocarbon groups (alkyl or aryl groups), we hypothesized that bisphenol compounds consisting of such groups also work bifunctionally. In the present study, we examined bisphenol AP (BPAP), B (BPB), and Z (BPZ). After recognizing their considerably strong receptor binding affinities, we evaluated the abilities of BPAP, BPB, and BPZ to activate ER alpha and ER beta in a luciferase reporter gene assay. These bisphenols were fully active for ER alpha but completely inactive for ER beta. When we examined their inhibitory activities for 17 beta-estradiol in ER beta by two different qualitative and quantitative analytical methods, we found that those bisphenols worked as definite antagonists. Consequently, they were established as bifunctional ER alpha-agonists and ER beta antagonists. The present structure-activity analyses revealed that the dispersion force works not only on the halogens but also on the hydrocarbon groups, and that it is a major driving force of bifunctional ER alpha agonist and ER beta-antagonist activities.(c) 2021 Elsevier B.V. All rights reserved.