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Lin, C., Chen, D.-R., Hsieh, W.-C., Yu, W.-F., Lin, C.-C., Ko, M.-H., Juan, C.-H., Tsuang, B.-J. and Lin, P.-H. (2013) Investigation of the Cumulative Body Burden of Estrogen-3,4-Quinone in Breast Cancer Patients and Controls Using Albumin Adducts as Biomarkers. Toxicology Letters, 218, 194-199.
https://doi.org/10.1016/j.toxlet.2013.02.004

has been cited by the following article:

• TITLE: Steroids, Tri- and Meroterpenoids with a Quinone Structure—A Review

  AUTHORS: Maryam S. M. Aghaei, Thies Thiemann

  KEYWORDS: Steroid, Secosteroid, Meroterpenoid, Triterpenoid, Quinone, Anti-Tumour Agent, Antibiotic, Natural Product

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.14 No.1, March 29, 2024

  ABSTRACT: Terpenoids with quinoid structures are found as natural products. This includes steroidal quinones, quinones with a secosteroid structure and meroterpenoid quinones. Importantly, catechol estrogens as endogenous metabolites of estradiol and estrone are precursors of reactive quinones and semiquinones, which are thought to contribute to estrogen-induced carcinogenesis. On the other hand, a number of quinones that include substituted naphthoquinones and anthraquinones are highly cytotoxic and have been used in cancer treatment. This makes the structures interesting synthetic targets. The following is a review of important natural and synthetic terpenoid and steroid quinone hybrids.