glycyrrhetinic acid has been researched along with 11-deoxy glycyrrhetinic acid in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (16.67) | 29.6817 |
2010's | 4 (66.67) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
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, SE | 1 |
Chen, H; Chen, JJ; Geng, CA; Huang, XY; Luo, J; Ma, YB; Wang, LJ; Zhang, XM | 1 |
Ge, GB; Hao, DC; Hou, J; Jin, Q; Li, YG; Wang, P; Yang, L; Zhou, K; Zou, LW | 1 |
Hao, XJ; Huang, LR; Li, QJ; Luo, H; Wang, DP; Yang, XS; Zhang, JX | 1 |
Fukushima, EO; Muranaka, T; Nomura, Y; Vo, NNQ | 1 |
Shen, P; Wang, W; Yu, B; Zhang, J; Zhu, Y | 1 |
6 other study(ies) available for glycyrrhetinic acid and 11-deoxy glycyrrhetinic acid
Article | Year |
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Naturally occurring pentacyclic triterpenes as inhibitors of glycogen phosphorylase: synthesis, structure-activity relationships, and X-ray crystallographic studies.
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, biological evaluation and structure-activity relationships of glycyrrhetinic acid derivatives as novel anti-hepatitis B virus agents.
Topics: Antiviral Agents; DNA Replication; DNA, Viral; Glycyrrhetinic Acid; Hepatitis B virus; Structure-Activity Relationship; Virus Replication | 2012 |
Design, synthesis, and structure-activity relationship study of glycyrrhetinic acid derivatives as potent and selective inhibitors against human carboxylesterase 2.
Topics: Carboxylesterase; Drug Design; Enzyme Inhibitors; Glycyrrhetinic Acid; Humans; Molecular Docking Simulation; Structure-Activity Relationship | 2016 |
18β-Glycyrrhetinic Acid Derivatives Possessing a Trihydroxylated A Ring Are Potent Gram-Positive Antibacterial Agents.
Topics: Ampicillin; Anti-Bacterial Agents; Bacillus subtilis; Dose-Response Relationship, Drug; Glycyrrhetinic Acid; Glycyrrhiza; Gram-Positive Bacteria; Methicillin-Resistant Staphylococcus aureus; Microbial Sensitivity Tests; Molecular Structure; Pseudomonas aeruginosa; Real-Time Polymerase Chain Reaction; Streptomyces; Streptomycin; Structure-Activity Relationship; Vancomycin | 2016 |
Structure-Activity Relationships of Pentacyclic Triterpenoids as Inhibitors of Cyclooxygenase and Lipoxygenase Enzymes.
Topics: Cyclooxygenase Inhibitors; Drug Evaluation, Preclinical; Humans; Lipoxygenase Inhibitors; Pentacyclic Triterpenes; Structure-Activity Relationship | 2019 |
Microbial transformation of glycyrrhetinic acid derivatives by Bacillus subtilis ATCC 6633 and Bacillus megaterium CGMCC 1.1741.
Topics: Animals; Anti-Inflammatory Agents; Bacillus megaterium; Bacillus subtilis; Biotransformation; Dose-Response Relationship, Drug; Glycyrrhetinic Acid; Lipopolysaccharides; Mice; Molecular Conformation; Nitric Oxide; RAW 264.7 Cells; Stereoisomerism; Structure-Activity Relationship | 2020 |