Recent Advances in Ent-Abietane Diterpenes: Natural Sources, Biological Activities and Total Synthesis

<i>Ent</i>-abietane diterpenoids constitute a class of terpenes with a C<sub>20</sub> carbon skeleton that underlie a wide range of biological activities. <i>Ent</i>-abietane diterpenoids, enantiomeric to the abietane counterparts, represent a family of diterpenoid natural products characterized by their distinct 6/6/6 tricyclic carbocyclic skeletons with exceptional structural complexity. An increasing number of these <i>ent</i>-abietane diterpenoids have recently been identified, constituting a well-defined group of naturally occurring compounds. This review provides a comprehensive summary of the natural sources, chemical structures, biological profiles and total synthesis of these <i>ent</i>-abietane diterpenoids from 2016 to early 2025.

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Journal
Molecules
Published
2025-12-25
DOI
https://doi.org/10.3390/molecules31010098
Primary Topic
Biological Activity of Diterpenoids and Biflavonoids
Type
article
Field-Weighted Citation Impact
0.00

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article

Recent Advances in Ent-Abietane Diterpenes: Natural Sources, Biological Activities and Total Synthesis

Zheng Chang-bo, Ji Li, Jian-Neng Yao, Yanan Zhu et al.
Molecules
Biological Activity of Diterpenoids and Biflavonoids
article

Recent Advances in Ent-Abietane Diterpenes: Natural Sources, Biological Activities and Total Synthesis

Zheng Chang-bo, Ji Li, Jian-Neng Yao, Yanan Zhu, L. Xie, Haixia Deng, Lu Li
article en

Abstract

<i>Ent</i>-abietane diterpenoids constitute a class of terpenes with a C<sub>20</sub> carbon skeleton that underlie a wide range of biological activities. <i>Ent</i>-abietane diterpenoids, enantiomeric to the abietane counterparts, represent a family of diterpenoid natural products characterized by their distinct 6/6/6 tricyclic carbocyclic skeletons with exceptional structural complexity. An increasing number of these <i>ent</i>-abietane diterpenoids have recently been identified, constituting a well-defined group of naturally occurring compounds. This review provides a comprehensive summary of the natural sources, chemical structures, biological profiles and total synthesis of these <i>ent</i>-abietane diterpenoids from 2016 to early 2025.

MoleculesVol. 31(1)
Kunming Medical University (CN)
National Natural Science Foundation of China, Kunming Medical University, Yunnan Key Research and Development Program
Openalex Percentile: Top 36%
Biological Activity of Diterpenoids and Biflavonoids
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