Bioactive enmein-type 6,7-seco-ent-kaurane diterpenoids: natural products, synthetic derivatives and apoptosis related mechanism
- PMID: 30242610
- DOI: 10.1007/s12272-018-1078-3
Bioactive enmein-type 6,7-seco-ent-kaurane diterpenoids: natural products, synthetic derivatives and apoptosis related mechanism
Abstract
Diterpenoids are important and widely distributed natural compounds with various biological effects, including antitumor, anti-inflammatory and so on. Great efforts have been put in phytochemistry research on diterpenoids. A number of structural modified derivatives and pharmacophore incorporated hybrids were also designed and synthesized with promising therapeutic effects. Among the hopefuls, enmein-type 6,7-seco-ent-kaurane diterpenoids with unique ring system and stereogenic centers exhibit attractive activities. Based on their lead-like properties, enmein-type diterpenoids are suitable for further medicinal study. The derivatives were biologically evaluated and showed promising activities, which warranted in-depth research for further understanding. In this review, the natural bioactive enmein-type diterpenoids and the synthetic derivatives were comprehensively summarized.
Keywords: 6,7-seco-ent-kaurane; Diterpenoid; Enmein-type; Natural product; Synthetic derivative.
Similar articles
-
Bioactive Natural Spirolactone-Type 6,7-seco-ent-Kaurane Diterpenoids and Synthetic Derivatives.Molecules. 2018 Nov 8;23(11):2914. doi: 10.3390/molecules23112914. Molecules. 2018. PMID: 30413071 Free PMC article. Review.
-
Synthesis, Cytotoxicity and Antimicrobial Activity of New Enmein-type Kauranoid Diterpenoid Derivatives.Anticancer Agents Med Chem. 2017;17(12):1679-1688. doi: 10.2174/1871521409666170412114648. Anticancer Agents Med Chem. 2017. PMID: 28403782
-
Cytotoxic diterpenoids from Pteris ensiformis.J Asian Nat Prod Res. 2017 Feb;19(2):188-193. doi: 10.1080/10286020.2016.1274307. J Asian Nat Prod Res. 2017. PMID: 28252343
-
The conversion of oridonin to spirolactone-type or enmein-type diterpenoid: synthesis and biological evaluation of ent-6,7-seco-oridonin derivatives as novel potential anticancer agents.Eur J Med Chem. 2012 Jun;52:242-50. doi: 10.1016/j.ejmech.2012.03.024. Epub 2012 Mar 23. Eur J Med Chem. 2012. PMID: 22483090
-
Recent progress in the development of natural ent-kaurane diterpenoids with anti-tumor activity.Mini Rev Med Chem. 2011 Sep;11(10):910-9. doi: 10.2174/138955711796575416. Mini Rev Med Chem. 2011. PMID: 21781025 Review.
Cited by
-
Isodon rubescens research literature based on Web of Science database for visual analysis: A review.Medicine (Baltimore). 2025 May 2;104(18):e41945. doi: 10.1097/MD.0000000000041945. Medicine (Baltimore). 2025. PMID: 40324265 Free PMC article. Review.
-
Therapeutic Potential of Terpenoids in Cancer Treatment: Targeting Mitochondrial Pathways.Cancer Rep (Hoboken). 2024 Sep;7(9):e70006. doi: 10.1002/cnr2.70006. Cancer Rep (Hoboken). 2024. PMID: 39234662 Free PMC article. Review.
-
Enmein Decreases Synaptic Glutamate Release and Protects against Kainic Acid-Induced Brain Injury in Rats.Int J Mol Sci. 2021 Nov 30;22(23):12966. doi: 10.3390/ijms222312966. Int J Mol Sci. 2021. PMID: 34884781 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
- 21772124/National Natural Science Foundation of China
- 21502121/National Natural Science Foundation of China
- 2017T100186/China Postdoctoral Science Foundation
- 20170540858/Natural Science Foundation of Liaoning Province
- 2017LQN05/General Scientific Research Projects of Department of Education in Liaoning Province
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous