Page last updated: 2024-08-17

spironolactone and oridonin

spironolactone has been researched along with oridonin in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Cai, H; Jiang, J; Li, D; Wang, L; Xu, J; Xu, S; Yao, H; Zhang, Y1
Cai, H; Jiang, B; Li, D; Liu, G; Sun, Y; Wang, L; Wang, Y; Wu, X; Xu, J; Yao, H1
He, C; Jia, Y; Ni, X; Wu, X; Xu, J; Xu, S; Yao, H; Zhou, K1

Other Studies

3 other study(ies) available for spironolactone and oridonin

ArticleYear
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.
    European journal of medicinal chemistry, 2012, Volume: 52

    Topics: Animals; Antineoplastic Agents; Chemistry Techniques, Synthetic; Diterpenes; Diterpenes, Kaurane; Female; Humans; K562 Cells; Mice; Spironolactone; Structure-Activity Relationship; Xenograft Model Antitumor Assays

2012
Synthesis of spirolactone-type diterpenoid derivatives from kaurene-type oridonin with improved antiproliferative effects and their apoptosis-inducing activity in human hepatoma Bel-7402 cells.
    European journal of medicinal chemistry, 2013, Volume: 59

    Topics: Antineoplastic Agents; Apoptosis; Cell Cycle; Cell Line, Tumor; Diterpenes; Diterpenes, Kaurane; Flow Cytometry; Humans; Inhibitory Concentration 50; Liver Neoplasms; Models, Molecular; Paclitaxel; Spironolactone

2013
Spirolactone-type and enmein-type derivatives as potential anti-cancer agents derived from oridonin.
    Bioorganic & medicinal chemistry, 2022, 10-15, Volume: 72

    Topics: Antineoplastic Agents; Apoptosis; Biological Products; Cell Line, Tumor; Cell Proliferation; Cyclin B1; Diterpenes; Diterpenes, Kaurane; Esters; Humans; Reactive Oxygen Species; Spironolactone; Structure-Activity Relationship

2022