Page last updated: 2024-08-24

ursolic acid and stigmasterol

ursolic acid has been researched along with stigmasterol in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (7.69)18.2507
2000's4 (30.77)29.6817
2010's8 (61.54)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Habib-Jiwan, JL; Hoet, S; Muccioli, GG; Opperdoes, FR; Pieters, L; Quetin-Leclercq, J1
Afza, N; Bibi, N; Farheen, S; Kazmi, SU; Malik, A; Siddiqi, S; Tanoli, SA; Zhang, Y1
Chin, YW; Jee, JG; Jeong, YJ; Keum, YS; Kim, Y; Lee, J; Lee, JM; Yu, MS1
Ahn, HC; Cho, SC; Choi, BY; Fei, X; Keum, YS; Kim, HJ; Lee, K; Seo, SY1
Alcaro, S; Corona, A; Cottiglia, F; Distinto, S; Floris, C; Fois, B; Maccioni, E; Malpure, NV; Meleddu, R; Sonar, VP; Tramontano, E1
Eid, HM; Haddad, PS; Kasangana, PB; Nachar, A; Stevanovic, T1
Xu, J; Xu, Y; Zheng, X1
Chen, X; Ishibashi, M; Li, Y; Ohizumi, Y; Oshima, Y; Satake, M1
Dallavalle, S; Jayasinghe, L; Kumarihamy, BM; Merlini, L; Musso, L; Scaglioni, L1
Ahmad, AS; Mansour, AI; Nafady, AM; Ramadan, MA1
Gao, TY; Li, CH; Tang, WZ; Wang, XJ1
Luo, P; Pan, W; Su, J; Wei, J; Wei, W; Zhu, Y1
Adewole, KE; Ishola, AA1

Other Studies

13 other study(ies) available for ursolic acid and stigmasterol

ArticleYear
Antitrypanosomal activity of triterpenoids and sterols from the leaves of Strychnos spinosa and related compounds.
    Journal of natural products, 2007, Volume: 70, Issue:8

    Topics: Animals; Benin; Cell Line, Tumor; Molecular Structure; Plant Leaves; Plants, Medicinal; Sterols; Stigmasterol; Structure-Activity Relationship; Strychnos; Triterpenes; Trypanocidal Agents; Trypanosoma brucei brucei

2007
In vitro antituberculosis activities of the constituents isolated from Haloxylon salicornicum.
    Bioorganic & medicinal chemistry letters, 2010, Jul-15, Volume: 20, Issue:14

    Topics: Antitubercular Agents; Chenopodiaceae; Colorimetry; In Vitro Techniques; Microbial Sensitivity Tests; Mycobacterium tuberculosis

2010
Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13.
    Bioorganic & medicinal chemistry letters, 2012, Jun-15, Volume: 22, Issue:12

    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
Discovery of α-mangostin as a novel competitive inhibitor against mutant isocitrate dehydrogenase-1.
    Bioorganic & medicinal chemistry letters, 2015, Dec-01, Volume: 25, Issue:23

    Topics: Binding, Competitive; Drug Discovery; Humans; Isocitrate Dehydrogenase; MCF-7 Cells; Molecular Structure; Mutation; Recombinant Proteins; Structure-Activity Relationship; Xanthones

2015
Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase.
    European journal of medicinal chemistry, 2017, Apr-21, Volume: 130

    Topics: Amides; Anti-HIV Agents; Binding Sites; Caffeic Acids; Coumaric Acids; DNA-Directed DNA Polymerase; Esters; HIV Reverse Transcriptase; Plant Extracts; Ribonuclease H, Human Immunodeficiency Virus; Structure-Activity Relationship; Triterpenes

2017
Bioactive Pentacyclic Triterpenes from the Root Bark Extract of Myrianthus arboreus, a Species Used Traditionally to Treat Type-2 Diabetes.
    Journal of natural products, 2018, 10-26, Volume: 81, Issue:10

    Topics: Cell Line; Diabetes Mellitus, Type 2; Enzyme Activation; Enzyme Inhibitors; Glucose; Glucose-6-Phosphatase; Glycogen Synthase; Hepatocytes; Humans; Hypoglycemic Agents; Molecular Structure; Pentacyclic Triterpenes; Plant Bark; Plant Extracts; Plant Roots; Urticaceae

2018
[Chemical studies on Pyrrosia gralla (Gies.) Ching].
    Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 1998, Volume: 23, Issue:2

    Topics: Drugs, Chinese Herbal; Molecular Structure; Plants, Medicinal; Stigmasterol; Triterpenes; Ursolic Acid; Xanthenes; Xanthones

1998
Sterol and triterpenoid constituents of Verbena littoralis with NGF-potentiating activity.
    Journal of natural products, 2003, Volume: 66, Issue:5

    Topics: Animals; Japan; Molecular Structure; Nerve Growth Factors; Neurites; Nuclear Magnetic Resonance, Biomolecular; Oleanolic Acid; PC12 Cells; Plants, Medicinal; Rats; Stereoisomerism; Stigmasterol; Triterpenes; Tumor Cells, Cultured; Ursolic Acid; Verbena

2003
A new 3,4-seco-lupane derivative from Lasianthus gardneri.
    Journal of natural products, 2004, Volume: 67, Issue:5

    Topics: Glucosides; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Pentacyclic Triterpenes; Plant Stems; Rubiaceae; Sitosterols; Sri Lanka; Stigmasterol; Triterpenes; Ursolic Acid

2004
Chemical composition of the stem bark and leaves of Ficus pandurata Hance.
    Natural product research, 2009, Volume: 23, Issue:13

    Topics: Betulinic Acid; Ficus; Magnetic Resonance Spectroscopy; Molecular Structure; Oleanolic Acid; Pentacyclic Triterpenes; Plant Bark; Plant Leaves; Sitosterols; Spectrophotometry, Infrared; Spectrophotometry, Ultraviolet; Stigmasterol; Triterpenes; Ursolic Acid

2009
[Chemical Constituents of Paulownia tomentosa Fruits].
    Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 2015, Volume: 38, Issue:3

    Topics: Flavanones; Fruit; Lamiales; Luteolin; Phytochemicals; Stigmasterol; Triterpenes; Ursolic Acid

2015
A new anthraquinone and eight constituents from Hedyotis caudatifolia Merr. et Metcalf: isolation, purification and structural identification.
    Natural product research, 2016, Volume: 30, Issue:19

    Topics: Anthraquinones; China; Hedyotis; Magnetic Resonance Spectroscopy; Molecular Structure; Oleanolic Acid; Plants, Medicinal; Sitosterols; Stigmasterol; Triterpenes; Ursolic Acid

2016
Phytosterols and triterpenes from Morinda lucida Benth. exhibit binding tendency against class I HDAC and HDAC7 isoforms.
    Molecular biology reports, 2019, Volume: 46, Issue:2

    Topics: Cholesterol; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Molecular Docking Simulation; Morinda; Oleanolic Acid; Phytosterols; Plant Extracts; Plant Leaves; Protein Isoforms; Stigmasterol; Triterpenes; Ursolic Acid

2019