Article citationsMore>>
Yildizhan, S., Van Loon, J., Sramkova, A., Ayasse, M., Aresene, C., Ten Broeke, C. and Schulz, S. (2009) Aphrodisiac Pheromones from the Wings of the Small Cabbage White and Large Cabbage White Butterflies, Pieris rapae and Pieris brassicae. ChemBioChem, 10, 1666-1677.
https://doi.org/10.1002/cbic.200900183
has been cited by the following article:
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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.