Page last updated: 2024-08-26

lupenone and betulin

lupenone has been researched along with betulin in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (25.00)29.6817
2010's6 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hata, K; Hori, K; Takahashi, S1
Bazzocchi, IL; Jiménez, IA; Moujir, L; Núñez, MJ; Reyes, CP1
Auwerx, J; Boudjelal, G; Genet, C; Lobstein, A; Saladin, R; Schmidt, C; Schoonjans, K; Souchet, M; Strehle, A; Wagner, A1
Estévez-Braun, A; Gordillo-Román, B; Gutiérrez-Nicolás, F; Joseph-Nathan, P; Oberti, JC; Ravelo, AG1
Alcamí, J; Bazzocchi, IL; Bedoya, LM; Beltrán, M; Calderón, PO; Callies, O; Jiménez, IA; Muñoz, A; Osorio, AA1
García-Cámara, I; Moo-Puc, RE; Peraza-Sánchez, SR; Torres-Tapia, LW; Valencia-Chan, LS1
Cen, YZ; Fan, X; Li, YL; Wang, YL; Xu, SY1
Feliciano, AS; Franco, LM; Oshima-Franco, Y; Puebla, P; Rubem-Mauro, L; Santos, MG; Silva, RV1

Other Studies

8 other study(ies) available for lupenone and betulin

ArticleYear
Differentiation- and apoptosis-inducing activities by pentacyclic triterpenes on a mouse melanoma cell line.
    Journal of natural products, 2002, Volume: 65, Issue:5

    Topics: Animals; Apoptosis; Betulinic Acid; Cell Differentiation; Inhibitory Concentration 50; Magnetic Resonance Spectroscopy; Melanoma, Experimental; Mice; Molecular Structure; Oxidation-Reduction; Pentacyclic Triterpenes; Pyridinium Compounds; Spectroscopy, Fourier Transform Infrared; Structure-Activity Relationship; Triterpenes; Tumor Cells, Cultured

2002
Lupane triterpenoids from Maytenus species.
    Journal of natural products, 2005, Volume: 68, Issue:7

    Topics: Animals; Antineoplastic Agents, Phytogenic; Bacteria; Betulinic Acid; Chlorocebus aethiops; Drug Screening Assays, Antitumor; HeLa Cells; Humans; Maytenus; Microbial Sensitivity Tests; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Pentacyclic Triterpenes; Peru; Triterpenes; Tumor Cells, Cultured

2005
Structure-activity relationship study of betulinic acid, a novel and selective TGR5 agonist, and its synthetic derivatives: potential impact in diabetes.
    Journal of medicinal chemistry, 2010, Jan-14, Volume: 53, Issue:1

    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
Synthesis and anti-HIV activity of lupane and olean-18-ene derivatives. Absolute configuration of 19,20-epoxylupanes by VCD.
    Journal of natural products, 2012, Apr-27, Volume: 75, Issue:4

    Topics: Anti-HIV Agents; Circular Dichroism; Crystallography, X-Ray; Molecular Structure; Stereoisomerism; Structure-Activity Relationship; Triterpenes

2012
Isolation, Structural Modification, and HIV Inhibition of Pentacyclic Lupane-Type Triterpenoids from Cassine xylocarpa and Maytenus cuzcoina.
    Journal of natural products, 2015, May-22, Volume: 78, Issue:5

    Topics: Anti-HIV Agents; Antineoplastic Agents, Phytogenic; Celastraceae; HIV-1; Humans; Maytenus; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Peru; Plant Bark; Plant Stems; Structure-Activity Relationship; Triterpenes

2015
Lupane-Type Triterpenes of Phoradendron vernicosum.
    Journal of natural products, 2017, 11-22, Volume: 80, Issue:11

    Topics: Antineoplastic Agents, Phytogenic; Drug Screening Assays, Antitumor; HeLa Cells; Humans; KB Cells; MCF-7 Cells; Mexico; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Phoradendron; Plant Components, Aerial; Plant Extracts; Plant Leaves; Triterpenes

2017
[Studies on the triterpenoids constituents from Phyllodium elegans].
    Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 2010, Volume: 33, Issue:5

    Topics: Fabaceae; Molecular Structure; Pentacyclic Triterpenes; Plant Leaves; Plant Stems; Plants, Medicinal; Triterpenes

2010
Chemical constituents of the bark of Dipteryx alata vogel, an active species against Bothrops jararacussu venom.
    Molecules (Basel, Switzerland), 2010, Nov-12, Volume: 15, Issue:11

    Topics: Animals; Bothrops; Crotalid Venoms; Diaphragm; Dipteryx; In Vitro Techniques; Isoflavones; Magnetic Resonance Spectroscopy; Male; Mass Spectrometry; Mice; Molecular Structure; Neuromuscular Blockade; Pentacyclic Triterpenes; Phrenic Nerve; Plant Bark; Plant Extracts; Triterpenes

2010