friedelin has been researched along with betulinic acid in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (38.46) | 29.6817 |
| 2010's | 8 (61.54) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Akhtar, MN; Choudhary, MI; Khan, SN; Zareen, S | 1 |
| Auwerx, J; Boudjelal, G; Genet, C; Lobstein, A; Saladin, R; Schmidt, C; Schoonjans, K; Souchet, M; Strehle, A; Wagner, A | 1 |
| Chin, YW; Jee, JG; Jeong, YJ; Keum, YS; Kim, Y; Lee, J; Lee, JM; Yu, MS | 1 |
| Batista-Gonzalez, A; Brunhofer, G; Fallarero, A; Gopi Mohan, C; Karlsson, D; Shinde, P; Vuorela, P | 1 |
| Ahn, HC; Cho, SC; Choi, BY; Fei, X; Keum, YS; Kim, HJ; Lee, K; Seo, SY | 1 |
| Pascoal Neto, C; Pinto, PC; Silvestre, AJ; Sousa, AF | 1 |
| Kuiate, JR; Mouokeu, S; Tane, P; Wabo, HK | 1 |
| Benny, TK; Manoharan, KP; Song, FJ; Yang, D | 1 |
| Beng, VP; Etoa, FX; Kuete, V; Lall, N; Mbaveng, AT; Metuno, R; Meyer, JJ; Ngadjui, BT; Ngameni, B; Wabo, GF | 1 |
| Blanchard, P; Charreau, B; Dang, BT; Derbré, S; Gény, C; Litaudon, M; Loirand, G; Pacaud, P; Rakolomalala, G; Randriamboavonjy, JI; Richomme, P; Rouger, C; Séraphin, D; Tonnerre, P | 1 |
| Hu, HJ; Liu, Q; Wang, ZT; Yang, L; Yang, YB | 1 |
| Alcântara, AFC; Araújo, CRR; Dessimoni-Pinto, NAV; Murta, SMF; Romanha, AJ; Sales-Junior, PA; Silva, RR; Silva, TM; Souza-Fagundes, EM; Takahashi, JA | 1 |
| Cai, YT; Geng, HW | 1 |
13 other study(ies) available for friedelin and betulinic acid
| Article | Year |
|---|---|
alpha-Glucosidase inhibitory activity of triterpenoids from Cichorium intybus.
Topics: alpha-Glucosidases; Cichorium intybus; Glycoside Hydrolase Inhibitors; Molecular Structure; Pentacyclic Triterpenes; Plants, Medicinal; Saccharomyces; Seeds; Triterpenes | 2008 |
Structure-activity relationship study of betulinic acid, a novel and selective TGR5 agonist, and its synthetic derivatives: potential impact in diabetes.
Topics: 3T3-L1 Cells; Animals; Betulinic Acid; CHO Cells; Cricetinae; Cricetulus; Male; Mice; Mice, Inbred C57BL; Molecular Conformation; Pentacyclic Triterpenes; Receptors, G-Protein-Coupled; Stereoisomerism; Structure-Activity Relationship; Triterpenes | 2010 |
Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13.
Topics: Adenosine Triphosphate; Antiviral Agents; Apigenin; Breast; Cell Line; Cell Proliferation; Colorimetry; DNA; DNA Helicases; Epithelial Cells; Female; Flavonoids; Fluorescence Resonance Energy Transfer; Hepacivirus; Humans; Hydrolysis; Inhibitory Concentration 50; Kinetics; Methyltransferases; RNA Helicases; Severe acute respiratory syndrome-related coronavirus; Species Specificity; Viral Nonstructural Proteins; Viral Proteins | 2012 |
Exploration of natural compounds as sources of new bifunctional scaffolds targeting cholinesterases and beta amyloid aggregation: the case of chelerythrine.
Topics: Acetylcholinesterase; Amyloid beta-Peptides; Benzophenanthridines; Binding Sites; Butyrylcholinesterase; Catalytic Domain; Cholinesterase Inhibitors; Humans; Isoquinolines; Kinetics; Molecular Docking Simulation; Structure-Activity Relationship | 2012 |
Discovery of α-mangostin as a novel competitive inhibitor against mutant isocitrate dehydrogenase-1.
Topics: Binding, Competitive; Drug Discovery; Humans; Isocitrate Dehydrogenase; MCF-7 Cells; Molecular Structure; Mutation; Recombinant Proteins; Structure-Activity Relationship; Xanthones | 2015 |
Triterpenic and other lipophilic components from industrial cork byproducts.
Topics: Betulinic Acid; Gas Chromatography-Mass Spectrometry; Pentacyclic Triterpenes; Plant Bark; Quercus; Triterpenes | 2006 |
Antidermatophytic triterpenoids from Syzygium jambos (L.) Alston (Myrtaceae).
Topics: Antifungal Agents; Betulinic Acid; Microbial Sensitivity Tests; Microsporum; Mitosporic Fungi; Nuclear Magnetic Resonance, Biomolecular; Oleanolic Acid; Pentacyclic Triterpenes; Plant Extracts; Syzygium; Trichophyton; Triterpenes | 2007 |
Triterpenoids from Eugenia grandis: structure elucidation by NMR spectroscopy.
Topics: Betulinic Acid; Deuterium; Magnetic Resonance Spectroscopy; Molecular Conformation; Oleanolic Acid; Pentacyclic Triterpenes; Protons; Reference Standards; Sensitivity and Specificity; Sitosterols; Stereoisomerism; Syzygium; Triterpenes | 2007 |
Antimicrobial activity of the methanolic extract, fractions and compounds from the stem bark of Irvingia gabonensis (Ixonanthaceae).
Topics: Anti-Infective Agents; Betulinic Acid; Cameroon; Candida; Cellulose; Diterpenes; Ellagic Acid; Gram-Negative Bacteria; Gram-Positive Bacteria; Microbial Sensitivity Tests; Oleanolic Acid; Pentacyclic Triterpenes; Plant Bark; Plant Extracts; Triterpenes | 2007 |
Advanced glycation inhibition and protection against endothelial dysfunction induced by coumarins and procyanidins from Mammea neurophylla.
Topics: Animals; Antineoplastic Agents, Phytogenic; Betulinic Acid; Biflavonoids; Catechin; Cell Survival; Coumarins; Endothelial Cells; Fruit; Glycation End Products, Advanced; Male; Mammea; Molecular Structure; Pentacyclic Triterpenes; Plant Bark; Plant Extracts; Plant Leaves; Proanthocyanidins; Rats; Rats, Wistar; Triterpenes; Xanthones | 2014 |
[Chemical constituents of Clerodendrum trichotomum Leaves].
Topics: Betulinic Acid; Clerodendrum; Indoles; Oleanolic Acid; Pentacyclic Triterpenes; Plant Leaves; Sitosterols; Sterols; Stigmasterol; Triterpenes | 2014 |
Constituents from stem barks of Luehea ochrophylla Mart and evaluation of their antiparasitic, antimicrobial, and antioxidant activities.
Topics: Animals; Anti-Infective Agents; Antioxidants; Antiparasitic Agents; Betulinic Acid; Chlorocebus aethiops; Drug Evaluation, Preclinical; Glucosides; Inhibitory Concentration 50; Magnetic Resonance Spectroscopy; Malvaceae; Pentacyclic Triterpenes; Plant Bark; Plant Extracts; Sitosterols; Sterols; Triterpenes; Vero Cells | 2017 |
[Chemical Constituents from the Roots of Rhodomyrtus tomentosa].
Topics: Betulinic Acid; Magnoliaceae; Pentacyclic Triterpenes; Plant Roots; Sitosterols; Triterpenes | 2016 |