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Relevant bibliographies by topics / Stilbenoidy

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Academic literature on the topic 'Stilbenoidy'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Stilbenoidy"

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Kambiranda, Devaiah, Sheikh Basha, Stephen Stringer, James Obuya, and Janana Snowden. "Multi-year Quantitative Evaluation of Stilbenoids Levels Among Selected Muscadine Grape Cultivars." Molecules 24, no. 5 (2019): 981. http://dx.doi.org/10.3390/molecules24050981.

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Stilbenoids such as t-piceid, t-resveratrol, ε-viniferins, and t-pterostilbene can differ significantly among grape cultivars and years due to variation in environmental conditions and subsequent stressors encountered during a year. This study evaluated diverse muscadine grape cultivars for their ability to consistently produce four major stilbenoids such as t-piceid, t-resveratrol, ε-viniferins, and t-pterostilbene irrespective of environmental changes that can impact their production. Berries from forty-two muscadine grape cultivars were collected for three years (2013, 2014, and 2015) to me

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Pawlus, Alison D., Pierre Waffo-Téguo, Jonah Shaver, and Jean-Michel Mérillon. "Stilbenoid chemistry from wine and the genus Vitis, a review." OENO One 46, no. 2 (2012): 57. http://dx.doi.org/10.20870/oeno-one.2012.46.2.1512.

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<p style="text-align: justify;">Stilbenoids are of great interest on account of their many promising biological activities, especially in regards to prevention and potential treatment of many chronic diseases associated with aging. The simple stilbenoid monomer, <em>E</em>-resveratrol, has received the most attention due to early<em> in vitro</em> and <em>in vivo</em> biological activities in anti-aging assays. Since <em>Vitis vinifera</em>, primarily in the form of wine, is a major dietary source of these compounds, there is a tremendous a

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Chai, Yuan-yuan, Fang Wang, Yan-li Li, Ke Liu, and Hui Xu. "Antioxidant Activities of Stilbenoids fromRheum emodiWall." Evidence-Based Complementary and Alternative Medicine 2012 (2012): 1–7. http://dx.doi.org/10.1155/2012/603678.

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Rheum emodiWall has been reported to possess protective effect in many inflammatory diseases and oxidative stress-related injuries. This study aims to investigate antioxidant power of stilbenoids fromR. emodiand then explore the material basis for its antioxidant potential. The most abundant stilbenoid piceatannol-4′-O-β-D-glucopyranoside (PICG) and its aglycon piceatannol (PICE) were isolated fromR. emodirhizome. Using well-accepted antioxidant chemicals as reference, antioxidant activity of these stilbenoids was examined by measuring DPPH and superoxide anion radical scavenging, ferric reduc

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Rathore, Rajendra, and Jay K. Kochi. "Vicinal-diaryl interactions in stilbenoid hydrocarbons as observed in the through-space charge delocalization of their cation radicals." Canadian Journal of Chemistry 77, no. 5-6 (1999): 913–21. http://dx.doi.org/10.1139/v99-081.

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The conformational preference of vicinal or 1,2-phenyl groups is probed in two classes of ring-substituted 1,2-diphenylbicyclooctene (stilbenoid) hydrocarbons 1a-1d and 2a-2c. UV-vis spectroscopy reveals, and X-ray crystallography verifies, the intramolecular (edge-to-face) orientation for the phenyl-phenyl interaction in stilbenoids 1a-1d. Most importantly, when two pairs of ortho-methyl substituents are present, the cofacial phenyl groups in the stilbenoid donors are established by X-ray crystallography and spectrally observed in the cation radicals (2a+.-2c+.) by the appearance of new bands

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Billet, Kévin, Magdalena Anna Malinowska, Thibaut Munsch, et al. "Semi-Targeted Metabolomics to Validate Biomarkers of Grape Downy Mildew Infection Under Field Conditions." Plants 9, no. 8 (2020): 1008. http://dx.doi.org/10.3390/plants9081008.

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Grape downy mildew is a devastating disease worldwide and new molecular phenotyping tools are required to detect metabolic changes associated to plant disease symptoms. In this purpose, we used UPLC-DAD-MS-based semi-targeted metabolomics to screen downy mildew symptomatic leaves that expressed oil spots (6 dpi, days post-infection) and necrotic lesions (15 dpi) under natural infections in the field. Leaf extract analyses enabled the identification of 47 metabolites belonging to the primary metabolism including 6 amino acids and 1 organic acid, as well as an important diversity of specialized

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Ball, Judith M., Fabricio Medina-Bolivar, Katelyn Defrates, et al. "Investigation of Stilbenoids as Potential Therapeutic Agents for Rotavirus Gastroenteritis." Advances in Virology 2015 (2015): 1–10. http://dx.doi.org/10.1155/2015/293524.

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Rotavirus (RV) infections cause severe diarrhea in infants and young children worldwide. Vaccines are available but cost prohibitive for many countries and only reduce severe symptoms. Vaccinated infants continue to shed infectious particles, and studies show decreased efficacy of the RV vaccines in tropical and subtropical countries where they are needed most. Continuing surveillance for new RV strains, assessment of vaccine efficacy, and development of cost effective antiviral drugs remain an important aspect of RV studies. This study was to determine the efficacy of antioxidant and anti-inf

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Mattio, Luce Micaela, Giorgia Catinella, Sabrina Dallavalle, and Andrea Pinto. "Stilbenoids: A Natural Arsenal against Bacterial Pathogens." Antibiotics 9, no. 6 (2020): 336. http://dx.doi.org/10.3390/antibiotics9060336.

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The escalating emergence of resistant bacterial strains is one of the most important threats to human health. With the increasing incidence of multi-drugs infections, there is an urgent need to restock our antibiotic arsenal. Natural products are an invaluable source of inspiration in drug design and development. One of the most widely distributed groups of natural products in the plant kingdom is represented by stilbenoids. Stilbenoids are synthesised by plants as means of protection against pathogens, whereby the potential antimicrobial activity of this class of natural compounds has attract

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Treml, Leláková, Šmejkal, et al. "Antioxidant Activity of Selected Stilbenoid Derivatives in a Cellular Model System." Biomolecules 9, no. 9 (2019): 468. http://dx.doi.org/10.3390/biom9090468.

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The stilbenoids, a group of naturally occurring phenolic compounds, are found in a variety of plants, including some berries that are used as food or for medicinal purposes. They are known to be beneficial for human health as anti-inflammatory, chemopreventive, and antioxidative agents. We have investigated a group of 19 stilbenoid substances in vitro using a cellular model of THP-1 macrophage-like cells and pyocyanin-induced oxidative stress to evaluate their antioxidant or pro-oxidant properties. Then we have determined any effects that they might have on the expression of the enzymes catala

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Laavola, Mirka, Tiina Leppänen, Mari Hämäläinen, et al. "IL-6 in Osteoarthritis: Effects of Pine Stilbenoids." Molecules 24, no. 1 (2018): 109. http://dx.doi.org/10.3390/molecules24010109.

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Interleukin-6 (IL-6) is involved in the pathogenesis of various inflammatory diseases, like rheumatoid arthritis (RA). In the present study, we investigated the role of IL-6 in osteoarthritis (OA) patients and the effects of the stilbenoids monomethyl pinosylvin and pinosylvin on the expression of the cartilage matrix components aggrecan and collagen II and the inflammatory cytokine IL-6 in human OA chondrocytes. Synovial fluid and plasma samples were obtained from 100 patients with severe OA [BMI 29.7 (8.3) kg/m2, age 72 (14) years, median (IQR); 62/38 females/males] undergoing total knee rep

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Kivimäki, Konsta, Tiina Leppänen, Mari Hämäläinen, Katriina Vuolteenaho, and Eeva Moilanen. "Pinosylvin Shifts Macrophage Polarization to Support Resolution of Inflammation." Molecules 26, no. 9 (2021): 2772. http://dx.doi.org/10.3390/molecules26092772.

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Pinosylvin is a natural stilbenoid found particularly in Scots pine. Stilbenoids are a group of phenolic compounds identified as protective agents against pathogens for many plants. Stilbenoids also possess health-promoting properties in humans; for instance, they are anti-inflammatory through their suppressing action on proinflammatory M1-type macrophage activation. Macrophages respond to environmental changes by polarizing towards proinflammatory M1 phenotype in infection and inflammatory diseases, or towards anti-inflammatory M2 phenotype, mediating resolution of inflammation and repair. In

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Dissertations / Theses on the topic "Stilbenoidy"

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Holst, Hans Christof. "Stilbenoide Sternsysteme Synthese und Eigenschaften /." [S.l. : s.n.], 2003. http://ArchiMeD.uni-mainz.de/pub/2003/0031/diss.pdf.

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Soomro, Shahid A. "Design, synthesis and photochemical studies of stilbenoid dendrimers." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=975958569.

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Moss, Ryan Kurtis. "Development and validation of methods for the investigation of wine stilbenoids." Thesis, University of British Columbia, 2014. http://hdl.handle.net/2429/50808.

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Stilbenoids are secondary plant metabolites responsible for the protection of grape vine from bacterial and fungal infection. Red wine has been shown to be a major source of these compounds in the human diet, where they display an array of health benefits. The first goal of our study was to develop and validate a robust and selective method for quantification of the major stilbenoids in red and white wine using ultra-high-performance liquid chromatography coupled with electrospray ionization/quadrupole time-of-flight mass spectrometry (UHPLC-ESI-Q-TOF)

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Ressler, Daniel. "Synthesis of Resveratrol Ester Derivatives." Digital Commons @ East Tennessee State University, 2013. https://dc.etsu.edu/etd/1234.

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The goal of this research project was to synthesize derivatives of transresveratrol. In order for resveratrol to be activated and used by the body it needs to bind to Human Serum Albumin (HSA), a protein in blood plasma. The derivatives were synthesized to improve the ability of resveratrol to enter cells as well as improve their ability to bind to HSA. The three derivatives that were synthesized have converted one of the hydroxyl groups on resveratrol to an ether with a methylene chain terminated by a carboxylic acid. By varying the lengths of the methylene chain we varied the water solubilit

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Karpouk, Elena. "Photochemie von ungesättigten Sternverbindungen Wirt-Gast-Systeme bei stilbenoiden Dendrimeren /." [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=971998450.

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Van, Cleve Shelley Marie. "Synthesis of a Resveratrol Glycinate Derivative." Digital Commons @ East Tennessee State University, 2011. https://dc.etsu.edu/etd/1312.

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Recently, the compound resveratrol has had media attention as an anti carcinogen. However, the bioavailability of resveratrol is low in the human system due to its hydrophobic nature. Therefore, it must be administered in high dosages to be effective. A plethora of derivatives have been synthesized that have the potential of resveratrol but sadly share low bioavailability. The first effort of this research was an attempt to produce a more hydrophilic ester of resveratrol. Failing this, the final product was synthesized using a glycine derivative to produce 4-[(1E)-2-(3,5-diacetyloxyphenyl)ethe

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Jing, Stanley Mofor. "Synthesis of Resveratrol Esters and Aliphatic Acids." Digital Commons @ East Tennessee State University, 2011. https://dc.etsu.edu/etd/1382.

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Resveratrol (RV) is a naturally occurring phytoalexin of the stilbenoid family produced by some plant species, and present in grape skin, peanuts, and red wine. It has been found to exhibit anti-cancer, anti-inflammatory, anti-viral, anti-aging, cardio protective, and anti-oxidant properties. Bioavailability is a huge setback that limits the potentials of RV. As a result, efforts have been made to design and synthesize RV esters and aliphatic acids in an attempt to increase its bioavailability, solubility in water, and possibly improving its biological activities. Resveratrol esters, 3,5,4'-tr

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Bisson, Jonathan. "Développements méthodologiques en chromatographie de partage : application aux stilbénoïdes." Thesis, Bordeaux 2, 2012. http://www.theses.fr/2012BOR22006/document.

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Les stilbénoïdes, sont des composés phénoliques majoritairement issus du règne végétal. La Vigne par l’intermédiaire du vin et du raisin est la principale source alimentaire de stilbènes. La mise en évidence de leur rôle dans les mécanismes de défense des plantes et leurs activités biologiques, y compris sur l’Homme, en font un sujet d’étude en plein essor. L’un des objectifs de cette thèse a été de développer un ensemble de stratégies à la fois analytiques et préparatives utilisant la Chromatographie de Partage Centrifuge (CPC) pour l’étude et l’obtention de ces molécules. Dans un premier tem

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Lambert, Carole. "Étude du rôle des stilbènes dans les défenses de la vigne contre les maladies du bois." Thesis, Bordeaux 2, 2011. http://www.theses.fr/2011BOR21910/document.

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Les maladies du bois de la vigne, par exemple le syndrome de l’esca et l’eutypiose, sont dues à des champignons qui se développent dans le xylème et dégradent les tissus ligneux. Elles sont en recrudescence depuis une vingtaine d’année dans tous les vignobles du monde. A ce jour, aucun traitement curatif n’est disponible alors que ces maladies engendrent généralement la mort de la plante. L’étude des relations hôte-parasite et notamment celle des réponses de défense de plante, est nécessaire pour la compréhension et le développement de nouvelles stratégies de lutte. Parmi les molécules de défe

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Gali, Meghanath. "Synthesis of Small Molecule Inhibitors of Janus Kinase 2, Phosphodiesterase IV, GABAA and NMDA receptors: Investigation of Mcmurry, Mannich and Chemoenzymatic Strategies." Scholar Commons, 2011. http://scholarcommons.usf.edu/etd/3110.

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Stilbenoids possess a wide range of biological properties such as, anticancer, antiplatelet aggregation, antiestrogenic, antibacterial, antifungal and antiatherogenic, etc. Owing to these therapeutic values, a great deal of attention attracted in the synthesis of derivatives of stilbenes. During the course of the study, G6 a novel stilbenoid was discovered, through high throughput screening, to be a potent inhibitor of mutated JAK2-V617F. The mutated JAK2 variant has been implicated in various myeloproliferative disorders (MPDs) including polycythemia vera (PV), essential thrombocythemia (ET)

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Books on the topic "Stilbenoidy"

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Motoo, Tori, and Asakawa Yoshinori, eds. The biochemistry of the stilbenoids. Chapman & Hall, 1995.

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Gorham, J. Biochemistry of the Stilbenoids (Biochemistry of Natural Products, No 1). Springer, 1995.

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Book chapters on the topic "Stilbenoidy"

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Shen, Tao, Chun-Feng Xie, Xiao-Ning Wang, and Hong-Xiang Lou. "Stilbenoids." In Natural Products. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_63.

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Duarte, Noélia, Cátia Ramalhete, Patrícia Rijo, Mariana Alves Reis, and Maria-José U. Ferreira. "Stilbenoids in Grapes and Wine." In Handbook of Dietary Phytochemicals. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1745-3_21-1.

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Waffo-Téguo, Pierre, Stéphanie Krisa, Alison D. Pawlus, Tristan Richard, Jean-Pierre Monti, and Jean-Michel Mérillon. "Grapevine Stilbenoids: Bioavailability and Neuroprotection." In Natural Products. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_74.

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Duarte, Noélia, Cátia Ramalhete, Patrícia Rijo, Mariana Alves Reis, and Maria-José U. Ferreira. "Stilbenoids in Grapes and Wine." In Handbook of Dietary Phytochemicals. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-4148-3_21.

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Yang, Tianhong, Lingling Fang, and Fabricio Medina-Bolivar. "Production and Biosynthesis of Bioactive Stilbenoids in Hairy Root Cultures." In Production of Plant Derived Natural Compounds through Hairy Root Culture. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-69769-7_3.

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Billet, Kevin, Magdalena Anna Malinowska, Thibaut Munsch, et al. "Stilbenoid-Enriched Grape Cane Extracts for the Biocontrol of Grapevine Diseases." In Progress in Biological Control. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-51034-3_9.

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Gorena, Tamara, Claudia Mardones, Carola Vergara, Vania Saez, and Dietrich von Baer. "Evaluation of the Potential of Grape Canes as a Source of Bioactive Stilbenoids." In ACS Symposium Series. American Chemical Society, 2015. http://dx.doi.org/10.1021/bk-2015-1203.ch022.

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Beetch, Megan, and Barbara Stefanska. "DNA Methylation in Anti-cancer Effects of Dietary Catechols and Stilbenoids: An Overview of Underlying Mechanisms." In Handbook of Nutrition, Diet, and Epigenetics. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-55530-0_104.

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Beetch, Megan, and Barbara Stefanska. "DNA Methylation in Anti-Cancer Effects of Dietary Catechols and Stilbenoids: An Overview of Underlying Mechanisms." In Handbook of Nutrition, Diet, and Epigenetics. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-31143-2_104-1.

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Xiao, Kai, Hong-Jun Zhang, Li-Jiang Xuan, Juan Zhang, Ya-Ming Xu, and Dong-Lu Bai. "Stilbenoids: Chemistry and bioactivities." In Bioactive Natural Products (Part N). Elsevier, 2008. http://dx.doi.org/10.1016/s1572-5995(08)80032-4.

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Conference papers on the topic "Stilbenoidy"

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Castellano, Gloria, Adela León, and Francisco Torrens. "Quantitative Structure-Antileukemic Activity Models of stilbenoids: A Theoretical Study." In MOL2NET 2018, International Conference on Multidisciplinary Sciences, 4th edition. MDPI, 2018. http://dx.doi.org/10.3390/mol2net-04-05903.

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Coya, C., A. L. Álvarez, M. Ramos, et al. "A fluorescent stilbenoid dendrimer for solution-processed blue light emitting diodes." In Photonics Europe, edited by Paul L. Heremans, Michele Muccini, and Eric A. Meulenkamp. SPIE, 2008. http://dx.doi.org/10.1117/12.781089.

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Kamarozaman, AS, N. Ahmat, MSM Johari, ZZ Hafiz, MI Adenan, and SAS Mohamad. "Isolation of tetramer stilbenoids from Shorea leprosula Miq., acetylcholinesterase inhibitory activity and molecular docking study." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399897.

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Stefanska, Barbara, Cayla Boycott, and Tony Yang. "Abstract PO-002: Epigenetic regulation of metabolic pathways in response of breast cancer cells to stilbenoids." In Abstracts: AACR Special Virtual Conference on Epigenetics and Metabolism; October 15-16, 2020. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.epimetab20-po-002.

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Hošek, J., V. Leláková, K. Jabubczyk та ін. "Influence of the structure of prenylated and non-prenylated stilbenoids on the NF-κB/AP-1 signalling pathway and cyclooxygenases/lipoxygenase inhibition". У GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608324.

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