maslinic acid has been researched along with corosolic acid in 25 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (28.00) | 29.6817 |
| 2010's | 16 (64.00) | 24.3611 |
| 2020's | 2 (8.00) | 2.80 |
| Authors | Studies |
|---|---|
| Liu, J; Ni, P; Sun, H; Wen, X; Wu, G; Wu, X; Zhang, L | 1 |
| 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 |
| Cheng, K; Liu, J; Sun, H; Xie, J; Zhang, P | 1 |
| Acebey-Castellon, IL; Bouthagane, N; Doan Thi Mai, H; Gangloff, SC; Hung, NV; Lavaud, C; Le Magrex Debar, E; Litaudon, M; Muhammad, D; Roseau, N; Sevenet, T; Voutquenne-Nazabadioko, L | 1 |
| 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, X | 1 |
| Camelio, AM; Cho, J; Claussen, KR; DiGiovanni, J; Nelson, AT; Siegel, D; Tremmel, L | 1 |
| Li, H; Tian, S; Wang, C; Wei, X; Wu, P; Xu, L; Xue, J | 1 |
| Choi, SU; Kim, CS; Kim, SY; Lee, KR; Oh, J; Subedi, L | 1 |
| Fukushima, EO; Muranaka, T; Nomura, Y; Vo, NNQ | 1 |
| Chen, C; Cheng, K; Dai, L; Hu, K; Li, H; Liu, L; Sun, H; Wen, X; Xu, Q; Yuan, H | 1 |
| Li, ZY; Lin, HW; Shen, Y; Shu, W; Wang, QH; Zhou, JB | 1 |
| Duan, HQ; Liu, P; Pan, Q; Yao, Z; Zhang, YW | 1 |
| Chen, J; Li, WL; Lv, H; Zhang, HQ | 1 |
| Kang, SH; Shi, YQ; Yang, CX | 1 |
| Fang, W; Tao, J | 1 |
| Bruni, R; Caligiani, A; Malavasi, G; Marseglia, A; Palla, G; Tognolini, M | 1 |
| Chen, G; Hu, N; Li, G; Liu, D; Liu, S; Suo, Y; Wu, H; You, J | 1 |
| Li, H; Ma, X; Rao, Z; Sun, Q; Wang, Q | 1 |
| Hu, YJ; Qi, J; Yang, J; Yu, BY | 1 |
| Cao, J; Peng, LQ; Xu, JJ | 1 |
| Dai, Z; Fan, F; Li, S; Liu, Y; Ma, X; Qu, G; Sun, Z; Wang, D; Zhang, L; Zhang, X | 1 |
| Bishayee, A; Deshmukh, RR; Kumar, P; Kumar, S; Sharma, H | 1 |
| Baba, K; Hiramatsu, R; Kataoka, T; Koeda, S; Suradej, B; Tanigaki, R; Waku, T | 1 |
| Hong, Y; Liu, X; Wang, X; Yang, W; Yin, X; Zeng, Z | 1 |
| Hong, Y; Huang, J; Ke, C; Liu, X; Yang, W; Yin, X; Yu, C; Zang, X | 1 |
1 review(s) available for maslinic acid and corosolic acid
| Article | Year |
|---|---|
Pentacyclic triterpenes: New tools to fight metabolic syndrome.
Topics: Animals; Heart; Humans; Insulin Resistance; Liver; Metabolic Syndrome; Muscle, Skeletal; Oleanolic Acid; Oxidative Stress; Pentacyclic Triterpenes; Triterpenes; Ursolic Acid | 2018 |
24 other study(ies) available for maslinic acid and corosolic acid
| Article | Year |
|---|---|
Pentacyclic triterpenes. Part 1: the first examples of naturally occurring pentacyclic triterpenes as a new class of inhibitors of glycogen phosphorylases.
Topics: Animals; Blood Glucose; Cyclization; Enzyme Inhibitors; Fasting; Glycogen Phosphorylase; Liver; Mice; Molecular Structure; Muscles; Rats; Triterpenes | 2005 |
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 |
Practical synthesis of bredemolic acid, a natural inhibitor of glycogen phosphorylase.
Topics: Animals; Glycogen Phosphorylase; Muscles; Oleanolic Acid; Rabbits; Stereoisomerism; Triterpenes | 2008 |
Triterpenoid saponins from Symplocos lancifolia.
Topics: Anti-Bacterial Agents; Enterococcus faecalis; Escherichia coli; Magnoliopsida; Microbial Sensitivity Tests; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plant Leaves; Pseudomonas aeruginosa; Saponins; Staphylococcus aureus; Triterpenes; Vietnam | 2011 |
Identification of pentacyclic triterpenes derivatives as potent inhibitors against glycogen phosphorylase based on 3D-QSAR studies.
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.
Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Cytokines; Female; Mice; Mice, Inbred Strains; Molecular Conformation; Oleanolic Acid; Oxygen; Skin; Triterpenes; Ursolic Acid | 2015 |
Bioactive Pentacyclic Triterpenoids from the Leaves of Cleistocalyx operculatus.
Topics: Animals; Drug Screening Assays, Antitumor; Drugs, Chinese Herbal; Hep G2 Cells; Humans; Interleukin-6; Macrophages; MCF-7 Cells; Mice; Molecular Structure; Myrtaceae; Nuclear Magnetic Resonance, Biomolecular; Oleanolic Acid; Pentacyclic Triterpenes; Plant Leaves; Triterpenes; Tumor Necrosis Factor-alpha | 2016 |
Bioactive Triterpenoids from the Twigs of Chaenomeles sinensis.
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 |
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 |
Synthesis and anti-inflammatory activity of saponin derivatives of δ-oleanolic acid.
Topics: Acetyl-CoA Carboxylase; AMP-Activated Protein Kinases; Animals; Anti-Inflammatory Agents; Dose-Response Relationship, Drug; Glycyrrhizic Acid; Humans; Interleukin-6; Liver; Macrophages; Male; Medicine, Chinese Traditional; Mice; Mice, Inbred BALB C; Oleanolic Acid; Pentacyclic Triterpenes; Phosphorylation; Sapogenins; Saponins; Tumor Necrosis Factor-alpha | 2021 |
[Study on chemical constituents of Potentilla chinensis Ser].
Topics: Flavones; Flavonoids; Molecular Structure; Oleanolic Acid; Plants, Medicinal; Potentilla; Sitosterols; Triterpenes | 2006 |
[Triterpenes from herb of Potentilla chinesis].
Topics: Animals; Antineoplastic Agents, Phytogenic; Cell Line; Cell Survival; Chromatography, High Pressure Liquid; Fibroblasts; HeLa Cells; Humans; Mice; Molecular Structure; Plants, Medicinal; Potentilla; Triterpenes | 2006 |
[Studies on the triterpenes from loquat leaf (Eriobotrya japonica)].
Topics: Chromatography, High Pressure Liquid; Chromatography, Thin Layer; Molecular Structure; Oleanolic Acid; Plant Leaves; Plants, Medicinal; Rosaceae; Triterpenes; Ursolic Acid | 2008 |
[Triterpenoids and steroids of root of Rubus biflorus].
Topics: Magnetic Resonance Spectroscopy; Molecular Structure; Oleanolic Acid; Plant Roots; Plants, Medicinal; Rosaceae; Sitosterols; Steroids; Triterpenes | 2008 |
[Chemical constituents from Sambucus chinensis].
Topics: Oleanolic Acid; Sambucus; Triterpenes | 2012 |
A simple GC-MS method for the screening of betulinic, corosolic, maslinic, oleanolic and ursolic acid contents in commercial botanicals used as food supplement ingredients.
Topics: Betulinic Acid; Dietary Supplements; Gas Chromatography-Mass Spectrometry; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Plants; Triterpenes; Ursolic Acid | 2013 |
Simultaneous determination of six triterpenic acids in some Chinese medicinal herbs using ultrasound-assisted dispersive liquid-liquid microextraction and high-performance liquid chromatography with fluorescence detection.
Topics: Betulinic Acid; Chromatography, High Pressure Liquid; Fluorescence; Limit of Detection; Liquid Phase Microextraction; Medicine, Chinese Traditional; Oleanolic Acid; Pentacyclic Triterpenes; Plants, Medicinal; Solvents; Triterpenes; Ultrasonics; Ursolic Acid | 2015 |
Probing the binding interaction of human serum albumin with three bioactive constituents of Eriobotrta japonica leaves: Spectroscopic and molecular modeling approaches.
Topics: Binding Sites; Circular Dichroism; Eriobotrya; Humans; Molecular Docking Simulation; Plant Leaves; Protein Binding; Protein Structure, Tertiary; Serum Albumin; Spectrometry, Fluorescence; Spectroscopy, Fourier Transform Infrared; Triterpenes | 2015 |
Integrating qualitative and quantitative characterization of Prunellae Spica by HPLC-QTOF/MS and HPLC-ELSD.
Topics: China; Chromatography, High Pressure Liquid; Cinnamates; Depsides; Drugs, Chinese Herbal; Molecular Structure; Prunella; Rosmarinic Acid; Tandem Mass Spectrometry; Triterpenes | 2016 |
Microcrystalline cellulose based matrix solid phase dispersion microextration for isomeric triterpenoid acids in loquat leaves by ultrahigh-performance liquid chromatography and quadrupole time-of-flight mass spectrometry.
Topics: Cellulose; Chromatography, High Pressure Liquid; Eriobotrya; Isomerism; Limit of Detection; Oleanolic Acid; Plant Leaves; Solid Phase Extraction; Solvents; Tandem Mass Spectrometry; Triterpenes; Ursolic Acid | 2016 |
Identification of a novel cytochrome P450 enzyme that catalyzes the C-2α hydroxylation of pentacyclic triterpenoids and its application in yeast cell factories.
Topics: Bioreactors; Catalysis; Crataegus; Cytochrome P-450 Enzyme System; Hydroxylation; Metabolic Engineering; Plasmids; Saccharomyces cerevisiae; Triterpenes | 2019 |
Asiatic Acid, Corosolic Acid, and Maslinic Acid Interfere with Intracellular Trafficking and N-Linked Glycosylation of Intercellular Adhesion Molecule-1.
Topics: A549 Cells; Cytokines; Endoplasmic Reticulum; Glycosylation; Golgi Apparatus; Humans; Intercellular Adhesion Molecule-1; Microscopy, Confocal; Pentacyclic Triterpenes; Polysaccharides; Protein Transport; Triterpenes | 2018 |
Synthesis of water soluble pentacyclic dihydroxyterpene carboxylic acid derivatives coupled amino acids and their inhibition activities on α-glucosidase.
Topics: alpha-Glucosidases; Amino Acids; Dose-Response Relationship, Drug; Glycoside Hydrolase Inhibitors; Humans; Molecular Conformation; Solubility; Structure-Activity Relationship; Triterpenes; Water | 2019 |
Semi-synthesis of C28-modified triterpene acid derivatives from maslinic acid or corosolic acid as potential α-glucosidase inhibitors.
Topics: alpha-Glucosidases; Chemistry Techniques, Synthetic; Glycoside Hydrolase Inhibitors; Humans; Models, Molecular; Molecular Docking Simulation; Saccharomyces cerevisiae; Triterpenes | 2020 |