Estrogenic activity of lignin-derivable alternatives to bisphenol A assessed via molecular docking simulations. Issue 36 (23rd June 2021)

• Record Type: Journal Article
• Authors: Amitrano, Alice; Mahajan, Jignesh S.; Korley, LaShanda T. J.; Epps, Thomas H.
• Is Part Of: RSC advances. Volume 11:Issue 36(2021)
• Page Start: 22149
• Page End: 22158
• Publication Date: 2021-06-23
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1ra02170b
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : This article explores lignin-derivable bisphenols as alternatives to bisphenol A – a suspected endocrine disruptor – by investigating their structure-activity relationships with respect to estrogen receptor alpha via molecular docking. Abstract : Lignin-derivable bisphenols are potential alternatives to bisphenol A (BPA), a suspected endocrine disruptor; however, a greater understanding of structure–activity relationships (SARs) associated with such lignin-derivable building blocks is necessary to move replacement efforts forward. This study focuses on the prediction of bisphenol estrogenic activity (EA) to inform the design of potentially safer BPA alternatives. To achieve this goal, the binding affinities to estrogen receptor alpha (ERα) of lignin-derivable bisphenols were calculated via molecular docking simulations and correlated to median effective concentration (EC50 ) values using an empirical correlation curve created from known EC50 values and binding affinities of commercial (bis)phenols. Based on the correlation curve, lignin-derivable bisphenols with binding affinities weaker than ∼−6.0 kcal mol −1 were expected to exhibit no EA, and further analysis suggested that having two methoxy groups on an aromatic ring of the bio-derivable bisphenol was largely responsible for the reduction in binding to ERα. Such dimethoxy aromatics are readily sourced from the depolymerization of hardwood biomass. Additionally, bulkier substituents on the bridging carbon of lignin-bisphenols, like diethyl or dimethoxy, were shown to weaken binding to ERα. And, as the bio-derivable aromatics maintain major structural similarities to BPA, the resultant polymeric materials should possess comparable/equivalent thermal ( e.g., glass transition temperatures, thermal decomposition temperatures) and mechanical ( e.g., tensile strength, modulus) properties to those of polymers derived from BPA. Hence, the SARs established in this work can facilitate the development of sustainable polymers that maintain the performance of existing BPA-based materials while simultaneously reducing estrogenic potential.