Page last updated: 2024-08-21

oleanolic acid and 23-hydroxybetulinic acid

oleanolic acid has been researched along with 23-hydroxybetulinic 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's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
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
Aquino, R; Capasso, A; Festa, M; Mencherini, T; Picerno, P; Russo, P1
Ge, GB; Li, YC; Lin, S; Song, YQ; Tian, GH; Xia, GY; Zhang, JF; Zhong, WC1
Jiang, J; Liu, J; Wu, X; Xu, J; Yao, H; Ye, W; Zhang, H; Zhu, P1

Other Studies

5 other study(ies) available for oleanolic acid and 23-hydroxybetulinic acid

ArticleYear
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
Triterpenoid constituents from the roots of Paeonia rockii ssp. rockii.
    Journal of natural products, 2011, Oct-28, Volume: 74, Issue:10

    Topics: Amino Acid Chloromethyl Ketones; Antineoplastic Agents, Phytogenic; Apoptosis; Betulinic Acid; Biphenyl Compounds; Caspase Inhibitors; Drug Screening Assays, Antitumor; HEK293 Cells; HT29 Cells; Humans; Italy; Oleanolic Acid; Paeonia; Pentacyclic Triterpenes; Picrates; Plant Roots; Triterpenes

2011
Bioactivity-Guided Discovery of Human Carboxylesterase Inhibitors from the Roots of
    Journal of natural products, 2020, 10-23, Volume: 83, Issue:10

    Topics: Carboxylesterase; Cell Line, Tumor; Enzyme Inhibitors; Glucosides; Humans; Molecular Structure; Monoterpenes; Paeonia; Plant Extracts; Plant Roots; Sesquiterpenes; Structure-Activity Relationship

2020
Synthesis and biological evaluation of ambradiolic acid as an inhibitor of glycogen phosphorylase.
    Fitoterapia, 2015, Volume: 100

    Topics: Animals; Enzyme Inhibitors; Glycogen Phosphorylase; Molecular Structure; Muscle, Skeletal; Oleanolic Acid; Pentacyclic Triterpenes; Rabbits; Structure-Activity Relationship; Triterpenes

2015