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Review
. 2021 Oct 31;26(21):6598.
doi: 10.3390/molecules26216598.

Phytochemistry and Pharmacological Activities of the Diterpenoids from the Genus Daphne

Affiliations
Review

Phytochemistry and Pharmacological Activities of the Diterpenoids from the Genus Daphne

Yi-Wen Nie et al. Molecules. .

Abstract

There are abundant natural diterpenoids in the plants of the genus Daphne from the Thymelaeaceae family, featuring a 5/7/6-tricyclic ring system and usually with an orthoester group. So far, a total of 135 diterpenoids has been isolated from the species of the genus Daphne, which could be further classified into three main types according to the substitution pattern of ring A and oxygen-containing functions at ring B. A variety of studies have demonstrated that these compounds exert a wide range of bioactivities both in vitro and in vivo including anticancer, anti-inflammatory, anti-HIV, antifertility, neurotrophic, and cholesterol-lowering effects, which is reviewed herein. Meanwhile, the fascinating structure-activity relationship is also concluded in this review in the hope of providing an easy access to available information for the synthesis and optimization of efficient drugs.

Keywords: Daphne; bioactivities; diterpenoid.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Classification and skeletons of diterpenoids from the genus Daphne.
Scheme 1
Scheme 1
Distribution of diterpenoids in the species of the genus Daphne.
Figure 2
Figure 2
Structures of 12-hydroxydaphnetoxins (154).
Figure 3
Figure 3
Structures of daphnetoxins (5583).
Figure 4
Figure 4
Structures of genkwanines (8495).
Figure 5
Figure 5
Skeleton of resiniferonoids (9697).
Figure 6
Figure 6
Structures of 1-alkyldaphnanes (98107).
Figure 7
Figure 7
Structures of other daphnane diterpenoids from the genus Daphne (108123).
Figure 8
Figure 8
Structures of tigliane-type diterpenoids (124133).
Figure 9
Figure 9
Structures of lathyrane-type diterpenoids (134135).
Scheme 2
Scheme 2
Heat map of the IC50 values (μM) of cytotoxicity of some diterpenoids in various carcinoma cell lines in vitro.
Figure 10
Figure 10
SAR of diterpenoids as antineoplastics.

References

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