Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud

Molecules. 2018 Apr 18;23(4):935. doi: 10.3390/molecules23040935.

Abstract

Diterpenoids are the focus of natural product drug discovery because of their great structural diversity and pronounced biological activities. Euphorbia fischeriana Steud is a Chinese traditional medicinal herb for curing edema, ascites, and cancer. This plant contains rich diterpenoids. Based on the carbon skeleton and substituents, it can be classified into thirteen subtypes: ent-abietane, daphnane, tigliane, ingenane, ent-atisane, ent-rosane, ent-kaurene, ent-kaurane, secotigliane, lathyrane, ent-pimarene, isopimarene and dimeric. In this paper, we reviewed the chemical structures and biological activities of 90 diterpenoids isolated from this medicinal herb. We hope that this work can serve as a reference for further research of these diterpenoids and lay the foundation for drug discovery.

Keywords: Euphorbia fischeriana Steud; bioactivity; diterpenoids.

Publication types

  • Review

MeSH terms

  • Diterpenes / chemistry*
  • Diterpenes / pharmacology*
  • Euphorbia / chemistry*
  • Humans
  • Structure-Activity Relationship

Substances

  • Diterpenes