| Literature DB >> 35465454 |
Tristesse C J Burton1, David C Lankin2, Dejan Nikolic2,3, Brian Guo2, Jianming Ju4, Birgit M Dietz2,3, Chun-Tao Che2, Djaja Djendoel Soejarto2,5, Richard B van Breemen3,6.
Abstract
A new isoflavonoid, xanthocerin J, along with previously described xanthocerin A, were isolated from a methanol extract of aerial parts of a traditional American Indian herb, Amorpha canescens Pursh (Asteraceae). The structures of these compounds were characterized using mass spectrometry and NMR based on an isolation protocol using magnetic microbead affinity selection screening (MagMASS) for ligands to the estrogen receptor alpha (ERα). These compounds bound to ERα from an active fraction that exhibited dose-dependent antiestrogenic activity in the in vitro Ishikawa assay. However, these compounds did not exhibit antiestrogenic activity in the cell-based Ishikawa assay. Xanthocerin A and J may exhibit synergistic or additive activity with other compounds found in A. canescens which needs further exploration. This work highlights the potential of A. canescens as a prospect for the future discovery of compounds for women's health related to estrogen pathways.Entities:
Keywords: Amorpha canescens; Antiestrogenic; Estrogen receptor-alpha; Magnetic microbead affinity selection; Xanthocerin A; Xanthocerin J; screening
Year: 2021 PMID: 35465454 PMCID: PMC9032482 DOI: 10.1016/j.phytol.2021.07.018
Source DB: PubMed Journal: Phytochem Lett ISSN: 1874-3900 Impact factor: 1.873