Antitumor and antibacterial derivatives of oridonin: A main composition of Dong-Ling-Cao

D Li, T Han, S Xu, T Zhou, K Tian, X Hu, K Cheng, Z Li… - Molecules, 2016 - mdpi.com
Isodon rubescens has been used as a traditional green tea for more than 1000 years and
many medicinal functions of I. rubescens are also very useful, such as its well-known …

Oridonin, a Promising ent-Kaurane Diterpenoid Lead Compound

D Li, T Han, J Liao, X Hu, S Xu, K Tian, X Gu… - International Journal of …, 2016 - mdpi.com
Oridonin belongs to ent-kaurane tetracyclic diterpenoid and was first isolated from Isodon
species. It exhibits inhibitory activities against a variety of tumor cells, and pharmacological …

Oridonin derivatives as potential anticancer drug candidates triggering apoptosis through mitochondrial pathway in the liver cancer cells

D Luo, Y Yi, K Peng, T Liu, J Yang, S Liu… - European journal of …, 2019 - Elsevier
The biological function of the natural ent-kaurene diterpenoid isolated from genus Isodon,
oridonin, has been intensively studied. However, its mechanism studies and clinical …

Synthesis of spirolactone-type diterpenoid derivatives from kaurene-type oridonin with improved antiproliferative effects and their apoptosis-inducing activity in human …

D Li, H Cai, B Jiang, G Liu, Y Wang, L Wang… - European Journal of …, 2013 - Elsevier
A series of novel spirolactone-type diterpenoid derivatives of oridonin (12a–j) were
designed and synthesized. All the target compounds showed improved anti-proliferative …

Design, synthesis and biological mechanisms research on 1, 2, 3-triazole derivatives of Jiyuan Oridonin A

Y Ke, W Wang, LF Zhao, JJ Liang, Y Liu… - Bioorganic & Medicinal …, 2018 - Elsevier
Two series of derivatives with 1, 2, 3-triazole as heterocyclic moiety of Jiyuan Oridonin A, a
new ent-kaurene diterpenoid which was isolated from genus Isodon rubescens, were …

A novel potent anticancer compound optimized from a natural oridonin scaffold induces apoptosis and cell cycle arrest through the mitochondrial pathway

S Xu, H Yao, S Luo, YK Zhang, DH Yang… - Journal of Medicinal …, 2017 - ACS Publications
The cytotoxicity of the natural ent-kaurene diterpenoid, oridonin, has been extensively
studied. However, the application of oridonin for cancer therapy was hampered primarily by …

Oridonin: A promising anticancer drug from China

W Zhang, Q Huang, ZC Hua - Frontiers in biology, 2010 - Springer
Oridonin, a diterpenoid isolated from Rabdosia rubescens (Hemsl.) Hara, has been proved
to possess remarkable anticancer activity, in addition to its potential in antiinflammation and …

Enmein-type diterpenoid analogs from natural kaurene-type oridonin: Synthesis and their antitumor biological evaluation

D Li, S Xu, H Cai, L Pei, H Zhang, L Wang… - European Journal of …, 2013 - Elsevier
A series of enmein-type diterpenoid analogs (11–20) derived from natural kaurene-type
diterpenoid oridonin were synthesized and biologically evaluated. All target compounds …

Synthesis, biological evaluation and cellular localization study of fluorescent derivatives of Jiyuan Oridonin A

C Zhou, JY Zhang, HB Liu, XY Tian, Y Liu… - European Journal of …, 2022 - Elsevier
Abstract Jiyuan Oridonin A (JOA) is a naturally occurring ent-kaurane diterpenoid that
exhibits significant potential in the field of anti-tumor drug development. However, its …

Induction of G2/M Phase Arrest and Apoptosis by Oridonin in Human Laryngeal Carcinoma Cells

N Kang, JH Zhang, F Qiu, S Chen… - Journal of natural …, 2010 - ACS Publications
Oridonin (1), an active component isolated from the plant Rabdosia rubescens, has been
reported to exhibit antitumor effects. In this study, the mechanism involved in 1-induced …