Compounds > maslinic acid
Page last updated: 2024-08-25

maslinic acid and epi-maslinic acid

maslinic acid has been researched along with epi-maslinic acid in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Liu, J; Ni, P; Sun, H; Wen, X; Wu, X; Zhang, L; Zhang, 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
Li, J; Li, JY; Qiu, WW; Shen, Q; Tang, J; Wang, B; Yang, F; Zou, H1
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
Camelio, AM; Cho, J; Claussen, KR; DiGiovanni, J; Nelson, AT; Siegel, D; Tremmel, L1
Choi, SU; Kim, CS; Kim, SY; Lee, KR; Oh, J; Subedi, L1

Other Studies

6 other study(ies) available for maslinic acid and epi-maslinic acid

ArticleYear
Pentacyclic triterpenes. Part 2: Synthesis and biological evaluation of maslinic acid derivatives as glycogen phosphorylase inhibitors.
    Bioorganic & medicinal chemistry letters, 2006, Volume: 16, Issue:3

    Topics: Animals; Enzyme Inhibitors; Glycogen Phosphorylase, Muscle Form; Muscles; Rabbits; Structure-Activity Relationship; Triterpenes

2006
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
Synthesis and biological evaluation of heterocyclic ring-substituted maslinic acid derivatives as novel inhibitors of protein tyrosine phosphatase 1B.
    Bioorganic & medicinal chemistry letters, 2009, Dec-01, Volume: 19, Issue:23

    Topics: Dose-Response Relationship, Drug; Drug Design; Enzyme Inhibitors; Molecular Conformation; Protein Tyrosine Phosphatase, Non-Receptor Type 1; Stereoisomerism; Structure-Activity Relationship; Triterpenes

2009
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
Synthesis of oxygenated oleanolic and ursolic acid derivatives with anti-inflammatory properties.
    Bioorganic & medicinal chemistry letters, 2015, Oct-01, Volume: 25, Issue:19

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Cytokines; Female; Mice; Mice, Inbred Strains; Molecular Conformation; Oleanolic Acid; Oxygen; Skin; Triterpenes; Ursolic Acid

2015
Bioactive Triterpenoids from the Twigs of Chaenomeles sinensis.
    Journal of natural products, 2017, 04-28, Volume: 80, Issue:4

    Topics: Animals; Antineoplastic Agents, Phytogenic; Drug Screening Assays, Antitumor; Humans; Lipopolysaccharides; Microglia; Molecular Structure; Nerve Growth Factor; Neuroprotective Agents; Nitric Oxide; Plant Components, Aerial; Republic of Korea; Rosaceae; Triterpenes

2017