Compounds > oleanolic acid
Page last updated: 2024-08-21

oleanolic acid and 3-oxo-12-ursen-28-oic acid

oleanolic acid has been researched along with 3-oxo-12-ursen-28-oic acid in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's2 (40.00)2.80

Authors

AuthorsStudies
Boumediene, K; Da Nascimento, S; Dassonville-Klimpt, A; Galéra, P; Gnoatto, SC; Gosmann, G; Moslemi, S; Sonnet, P1
Alexacou, KM; Cheng, K; Gimisis, T; Hao, J; Hayes, JM; Leonidas, DD; Liu, J; Ni, P; Oikonomakos, NG; Sun, H; Wen, X; Zhang, L; Zhang, P; Zographos, SE1
Chen, J; Chen, L; Cheng, K; Gong, Y; Hao, J; Jiang, H; Li, H; Li, L; Liang, Z; Liu, H; Liu, J; Luo, C; Sun, H; Wen, X; Zhang, L; Zhang, P; Zhang, X; Zheng, M; Zhu, X1
An, LK; Hu, DX; Xiao, LG; Yan, XL; Yu, Q; Zhang, HL; Zhang, Y1
Adámek, R; Borková, L; Frydrych, I; Gurská, S; Hajdúch, M; Jakubcová, N; Lišková, B; Medvedíková, M; Urban, M1

Other Studies

5 other study(ies) available for oleanolic acid and 3-oxo-12-ursen-28-oic acid

ArticleYear
Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition.
    European journal of medicinal chemistry, 2008, Volume: 43, Issue:9

    Topics: Acetylation; Amides; Aromatase; Aromatase Inhibitors; Dose-Response Relationship, Drug; Esterification; Humans; Ilex paraguariensis; Inhibitory Concentration 50; Oxidation-Reduction; Triterpenes; Ursolic Acid

2008
Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies.
    Journal of medicinal chemistry, 2008, Jun-26, Volume: 51, Issue:12

    Topics: Adenosine Monophosphate; Allosteric Site; Animals; Binding Sites; Crystallography, X-Ray; Glycogen Phosphorylase; Hypoglycemic Agents; Kinetics; Models, Molecular; Muscles; Oleanolic Acid; Pentacyclic Triterpenes; Protein Binding; Protein Conformation; Rabbits; Stereoisomerism; Structure-Activity Relationship; Triterpenes

2008
Identification of pentacyclic triterpenes derivatives as potent inhibitors against glycogen phosphorylase based on 3D-QSAR studies.
    European journal of medicinal chemistry, 2011, Volume: 46, Issue:6

    Topics: Animals; Enzyme Inhibitors; Glycogen Phosphorylase, Muscle Form; Models, Molecular; Molecular Conformation; Muscle, Skeletal; Pentacyclic Triterpenes; Quantitative Structure-Activity Relationship; Rabbits; Stereoisomerism

2011
Secondary metabolites from Isodon ternifolius (D. Don) Kudo and their anticancer activity as DNA topoisomerase IB and Tyrosyl-DNA phosphodiesterase 1 inhibitors.
    Bioorganic & medicinal chemistry, 2020, 06-01, Volume: 28, Issue:11

    Topics: Animals; Antineoplastic Agents, Phytogenic; Cattle; Cell Proliferation; Cell Survival; DNA Topoisomerases, Type I; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Humans; Isodon; Molecular Structure; Phosphodiesterase Inhibitors; Phosphoric Diester Hydrolases; Structure-Activity Relationship; Topoisomerase I Inhibitors; Tumor Cells, Cultured

2020
Synthesis and biological evaluation of triterpenoid thiazoles derived from betulonic acid, dihydrobetulonic acid, and ursonic acid.
    European journal of medicinal chemistry, 2020, Jan-01, Volume: 185

    Topics: Antineoplastic Agents; Apoptosis; Cell Proliferation; Cells, Cultured; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Fibroblasts; Humans; Membrane Potential, Mitochondrial; Microsomes; Molecular Structure; Oleanolic Acid; Structure-Activity Relationship; Terpenes; Thiazoles; Triterpenes

2020