Ortega, H.E., Graupner, P.R., Asai, Y., Ten Dyke, K., Qiu, D., Shen, Y.Y., Rios, N., Arnold, A.E., Coley, P.D., Kursar, T.A., Gerwick, W.H. and Cubilla-Rios, L. (2013) Mycoleptodiscins A and B, Cytotoxic Alkaloids from the Endophytic Fungus Mycoleptodiscus Sp. F0194. Journal of Natural Products, 76, 741-744.
https://doi.org/10.1021/np300792t

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.