Academic literature on the topic 'Ellagic acid derivatives'

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Journal articles on the topic "Ellagic acid derivatives"

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Simões-Pires, Claudia A., Sandra Vargas, Andrew Marston, et al. "Ellagic Acid Derivatives from Syzygium cumini Stem Bark: Investigation of their Antiplasmodial Activity." Natural Product Communications 4, no. 10 (2009): 1934578X0900401. http://dx.doi.org/10.1177/1934578x0900401012.

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Bioguided fractionation of Syzygium cumini (Myrtaceae) bark decoction for antiplasmodial activity was performed, leading to the isolation of three known ellagic acid derivatives (ellagic acid, ellagic acid 4-O-α-L-2″-acetylrhamnopyranoside, 3-O-methylellagic acid 3′-O-α-L-rhamnopyranoside), as well as the new derivative 3-O-methylellagic acid 3′-O-β-D-glucopyranoside. Activity investigation was based on the reduction of P. falciparum (PfK1) parasitaemia in vitro and the inhibition of β-hematin formation, a known mechanism of action of some antimalarial drugs. Among the investigated ellagic aci
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Sullim Lee, Et al. "In Silico Screening of Ellagic Acid Derivatives and Their Metabolites as Inhibitors for NF-?b and Tnf?" International Journal on Recent and Innovation Trends in Computing and Communication 11, no. 9 (2023): 3160–65. http://dx.doi.org/10.17762/ijritcc.v11i9.9465.

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The aim of this study was to evaluate inhibitory effects of ellagic acid derivatives and their metabolites on tumor necrosis factor ? (TNF?) and nuclear factor-?B (NF-?B). In silico molecular docking was performed. 3-O-methyl-3', 4' -methylenedioxy ellagic acid (MMDEA) and urolithin D were to be potent inhibitors of TNF? among tested molecules. For NF-?B (p50 and p65 subunits), MMDEA was found to be a potent inhibitor comparable with tanshinone IIA, a known NF-?B inhibitor. Ellagic acid derivatives seemed to be more effective than urolithins, their metabolites. All of the ellagic acid derivati
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Tadzhibav, M. M., É. Kh Batirov, A. D. Vdovin, V. M. Malikov, K. L. Lutfullin, and M. R. Yagudaev. "Ellagic acid derivatives fromEuphorbia ferganensis." Chemistry of Natural Compounds 23, no. 5 (1987): 630–31. http://dx.doi.org/10.1007/bf00598694.

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Choi, Young-Hee, John Pezzuto, A. Kinghorn, and Norman Farnsworth. "Ellagic Acid Derivatives ofAgrostistachys hookeri1." Planta Medica 54, no. 06 (1988): 511–13. http://dx.doi.org/10.1055/s-2006-962532.

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Filho, Wilson Wolter, Arnaldo I. Da Rocha, Massayoshi Yoshida, and Otto R. Gottlieb. "Ellagic acid derivatives from Rhabdodendron macrophyllum." Phytochemistry 24, no. 9 (1985): 1991–93. http://dx.doi.org/10.1016/s0031-9422(00)83107-6.

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Li, Xing-Cong, Hala N. Elsohly, Charles D. Hufford, and Alice M. Clark. "NMR assignments of ellagic acid derivatives." Magnetic Resonance in Chemistry 37, no. 11 (1999): 856–59. http://dx.doi.org/10.1002/(sici)1097-458x(199911)37:11<856::aid-mrc529>3.0.co;2-x.

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Djoukeng, Jules Desire, Eliane Abou-Mansour, Leon Azefack Tapondjou, David Lontsi, and Raffaele Tabacchi. "Identification of Ellagic Acid Derivatives from Stem Bark of Syzygium Guineense (Myrtaceae)." Natural Product Communications 2, no. 3 (2007): 1934578X0700200. http://dx.doi.org/10.1177/1934578x0700200307.

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An LC-DAD-ESI-MSn technique was developed to investigate crude extracts of the stem bark of S. guineense for phenolic compounds. Ellagic acids were detected on the basis of their UV absorption spectra and ESI-MS fragmentation patterns. Six ellagic acid conjugates in the complex extract of S. guineense were identified. With the aim to confirm the structures, further purification of the extract afforded the known 3-O-ellagic acid-4′-O-α-rhampyranonosides (3), two new ellagic acid rhamnopyranosides, 3-O-methylellagic acid-4′-O-α-2″-O-acetylrhamnopyranoside (4) and 3-O-methylellagic acid-4′-O-α-3″
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Xu, Ya-ming, Jing-Zhen Deng, Ji Ma, et al. "DNA damaging activity of ellagic acid derivatives." Bioorganic & Medicinal Chemistry 11, no. 7 (2003): 1593–96. http://dx.doi.org/10.1016/s0968-0896(02)00452-2.

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Heur, Young-Hun, Wenguang Zeng, Gary D. Stoner, Gregory A. Nemeth, and Bruce Hilton. "Synthesis of Ellagic Acid O-Alkyl Derivatives and Isolation of Ellagic Acid as a Tetrahexanoyl Derivative from Fragaria ananassa." Journal of Natural Products 55, no. 10 (1992): 1402–7. http://dx.doi.org/10.1021/np50088a003.

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Salih, Enass Y. A., Riitta Julkunen-Tiitto, Olavi Luukkanen, Marketta Sipi, Mustafa K. M. Fahmi, and Pia Johanna Fyhrquist. "Potential Anti-Tuberculosis Activity of the Extracts and Their Active Components of Anogeissus leiocarpa (DC.) Guill. and Perr. with Special Emphasis on Polyphenols." Antibiotics 9, no. 7 (2020): 364. http://dx.doi.org/10.3390/antibiotics9070364.

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In Sudanese traditional medicine, decoctions of the stem bark of Anogeissus leiocarpa are used for the treatment of tuberculosis (TB). However, this plant has not been investigated before for its antimycobacterial effects. Our screening results show, for the first time, that many extracts of various parts of A. leiocarpa exhibit growth inhibitory activity against Mycobacterium smegmatis. Minimum inhibitory concentration (MIC) values ranged between 625 and 5000 µg/mL, with an ethyl acetate extract of the root showing the lowest MIC value. The good antimycobacterial effects of the root part coul
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Dissertations / Theses on the topic "Ellagic acid derivatives"

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Przewloka, Simon. "An investigation into commercially feasible applications of ellagic acid and its derivatives." Thesis, The Author [Mt. Helen, Vic.] :, 1999. http://researchonline.federation.edu.au/vital/access/HandleResolver/1959.17/35930.

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"Significant quantities of ellagic acid and its metal salts, in the form of waste byproducts, are readily available from both the pulping and tanning industries should a feasible commercial use for the acid (1) be found. The purpose of this work was to prepare key derivatives of ellagic acid and assess their feasibilty for use on a commercial scale. To accomplish this, it was first necessary to prepare ellagic acid in high yield."<br>Doctor of Philosophy
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Book chapters on the topic "Ellagic acid derivatives"

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Perchellet, Jean-Pierre, Hala U. Gali, Elisabeth M. Perchellet, Darren S. Klish, and Andrew D. Armbrust. "Antitumor-Promoting Activities of Tannic Acid, Ellagic Acid, and Several Gallic Acid Derivatives in Mouse Skin." In Plant Polyphenols. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3476-1_47.

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Alagawany, Mahmoud, Mohamed E. Abd El-Hack, Muhammad Saeed, Shaaban S. Elnesr, and Mayada R. Farag. "Clove (Syzygium aromaticum) and its Derivatives in Poultry Feed." In Antibiotic Alternatives in Poultry and Fish Feed. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815049015122010008.

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Production of safe and healthy poultry diets of high profitability is the central aim of poultry men. This safety is achieved by using natural products as growth stimulants. Natural feed additives such as medicinal products derived from herbs and spices are mainly used in the poultry feed industry as appetite and enzyme secretion stimulants. The use of clove (Syzygium aromaticum) and its derivatives has lately received much greater attention as an alternative to traditional antibiotics. The clove exhibited strong antibacterial, antioxidant, anti-septic and anti-inflammatory properties and appe
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Lorenzo, José M., Paulo E. Munekata, Predrag Putnik, Danijela Bursać Kovačević, Voster Muchenje, and Francisco J. Barba. "Sources, Chemistry, and Biological Potential of Ellagitannins and Ellagic Acid Derivatives." In Studies in Natural Products Chemistry. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-444-64181-6.00006-1.

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