Rearranged ergostane-type natural products: chemistry, biology, and medicinal aspects
Classical steroids are long-known privileged leads in drug discovery. Their rearranged counterparts, though, have so far received less attention, although recent isolation and biological testing programmes have revealed a plethora of molecular entities that are both structurally intriguing, as well...
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Veröffentlicht in: | Organic & biomolecular chemistry 2019-02, Vol.17 (7), p.1624-1633 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Classical steroids are long-known privileged leads in drug discovery. Their rearranged counterparts, though, have so far received less attention, although recent isolation and biological testing programmes have revealed a plethora of molecular entities that are both structurally intriguing, as well as biologically relevant. This review will highlight those natural products, and focus on ergostane-derived seco- and
abeo
-steroids. Their isolation, structure elucidation, and biological properties are reported. A special emphasis of this review lies in their respective (and typically proposed) biosyntheses, to help guide future bio-inspired synthetic attempts.
Rearranged ergostane-type natural products are structurally intriguing and exhibit biologically relevant properties. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c8ob02325e |