Academic literature on the topic 'Flavonoid Glucuronides'

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Journal articles on the topic "Flavonoid Glucuronides"

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Mues, Rüdiger, Gesine Leidinger, Vera Lauck, H. Dietmar Zinsmeister, Timo Koponen, and Kenneth R. Markham. "Rhizomnium magnifolium and R. pseudopunctatum, the First Mosses to Yield Flavone Glucuronides." Zeitschrift für Naturforschung C 41, no. 11-12 (1986): 971–75. http://dx.doi.org/10.1515/znc-1986-11-1203.

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Abstract Rhizomnium magnifolium and R. pseudopunctatum show an identical flavonoid pattern with six flavone glucuronides. Three of them; namely apometzgerin 7-O-glucuronide, selgin 7,5′-di-O-glucuronide and tricetin 7,3′-di-O-glucuronide are new natural compounds. This is the first report of flavonoid glucuronides in mosses.
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Yu, Yanhao, Yinquan Qu, Shuyang Wang, Qian Wang, Xulan Shang, and Xiangxiang Fu. "An Integrative Analysis of Metabolome and Transcriptome Reveals the Molecular Regulatory Mechanism of the Accumulation of Flavonoid Glycosides in Different Cyclocarya paliurus Ploidies." Forests 14, no. 4 (2023): 770. http://dx.doi.org/10.3390/f14040770.

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Cyclocarya paliurus (Batal) Iljinskaja is mainly used for harvesting leaves as materials for tea production and ingredients for the food industry. As its most important component, the contents of its total or specific flavonoids are supposed to vary at different ploidy levels. In the present study, two ploidy levels of C. paliurus are used to study their metabolome and transcriptome profiles. Though the total content of the flavonoids in leaves that were collected in September (the main harvesting season) presented insignificant differences between the two ploidies, flavonoid glucuronides were
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Bai, Yue, Lu Chen, Yun-Feng Cao, et al. "Beta-Glucuronidase Inhibition by Constituents of Mulberry Bark." Planta Medica 87, no. 08 (2021): 631–41. http://dx.doi.org/10.1055/a-1402-6431.

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AbstractIntestinal bacterial β-glucuronidases, the key enzymes responsible for the hydrolysis of various glucuronides into free aglycone, have been recognized as key targets for treating various intestinal diseases. This study aimed to investigate the inhibitory effects and mechanisms of the Mulberry bark constituents on E. coli β-glucuronidase (EcGUS), the most abundant β-glucuronidases produced by intestinal bacteria. The results showed that the flavonoids isolated from Mulberry bark could strongly inhibit E. coli β-glucuronidase, with IC50 values ranging from 1.12 µM to 10.63 µM, which were
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Uehara, Ayumi, Shinobu Akiyama, and Tsukasa Iwashina. "Foliar Flavonoids from Tanacetum vulgare var. boreale and their Geographical Variation." Natural Product Communications 10, no. 3 (2015): 1934578X1501000. http://dx.doi.org/10.1177/1934578x1501000307.

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Foliar flavonoids of Tanacetum vulgare var. boreale were isolated. Eight flavonoid glycosides, 7- O-glucosides of apigenin, luteolin, scutellarein and 6-hydroxyluteolin, and 7- O-glucuronides of apigenin, luteolin, chrysoeriol and eriodictyol were identified. Moreover, eight flavonoid aglycones, apigenin, luteolin, hispidulin, nepetin, eupatilin, jaceosidin, pectolinarigenin and axillarin were also isolated and identified. The flavonoid composition of two varieties of T. vulgare, i.e. var. boreale and var. vulgare, were compared. All samples of var. boreale and one sample of var. vulgare had t
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O'Leary, Karen A., Andrea J. Day, Paul W. Needs, William S. Sly, Nora M. O'Brien та Gary Williamson. "Flavonoid glucuronides are substrates for human liver β-glucuronidase". FEBS Letters 503, № 1 (2001): 103–6. http://dx.doi.org/10.1016/s0014-5793(01)02684-9.

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Adiji, Olubu A., Maite L. Docampo-Palacios, Anislay Alvarez-Hernandez, Giulio M. Pasinetti, Xiaoqiang Wang, and Richard A. Dixon. "UGT84F9 is the major flavonoid UDP-glucuronosyltransferase in Medicago truncatula." Plant Physiology 185, no. 4 (2021): 1617–37. http://dx.doi.org/10.1093/plphys/kiab016.

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Abstract Mammalian phase II metabolism of dietary plant flavonoid compounds generally involves substitution with glucuronic acid. In contrast, flavonoids mainly exist as glucose conjugates in plants, and few plant UDP-glucuronosyltransferase enzymes have been identified to date. In the model legume Medicago truncatula, the major flavonoid compounds in the aerial parts of the plant are glucuronides of the flavones apigenin and luteolin. Here we show that the M. truncatula glycosyltransferase UGT84F9 is a bi-functional glucosyl/glucuronosyl transferase in vitro, with activity against a wide rang
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Kamiya, Kohei, Yasuhisa Saiki, Takao Hama, et al. "Flavonoid glucuronides from Helicteres isora." Phytochemistry 57, no. 2 (2001): 297–301. http://dx.doi.org/10.1016/s0031-9422(01)00005-x.

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Afsharypuor, S., and G. B. Lockwood. "Flavonoid Glucuronides from Alyssum minimum." Journal of Natural Products 49, no. 5 (1986): 944–45. http://dx.doi.org/10.1021/np50047a041.

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Huang, Ying, Tess De Bruyne, Sandra Apers, et al. "Flavonoid glucuronides from Picria fel-terrae." Phytochemistry 52, no. 8 (1999): 1701–3. http://dx.doi.org/10.1016/s0031-9422(99)00242-3.

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Yang, Yan, Hui-Min Wang, Yuan-Feng Tong, et al. "Systems metabolic engineering of Escherichia coli to enhance the production of flavonoid glucuronides." RSC Advances 6, no. 40 (2016): 33622–30. http://dx.doi.org/10.1039/c6ra03304k.

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Dissertations / Theses on the topic "Flavonoid Glucuronides"

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Adiji, Olubu Adeoye. "Identification, Characterization and Engineering of UDP-Glucuronosyltransferases for Synthesis of Flavonoid Glucuronides." Thesis, University of North Texas, 2020. https://digital.library.unt.edu/ark:/67531/metadc1752363/.

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Flavonoids are polyphenolics compounds that constitute a major group of plant specialized metabolites, biosynthesized via the phenylpropanoid/polymalonate pathways. The resulting specialized metabolites can be due to decoration of flavonoid compounds with sugars, usually glucose, by the action of regiospecific UDP-glycosyltransferase (UGT) enzymes. In some cases, glycosylation can involve enzymatic attachment of other sugar moieties, such as glucuronic acid, galactose, rhamnose or arabinose. These modifications facilitate or impact the bioactivity, stability, solubility, bioavailability and ta
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Book chapters on the topic "Flavonoid Glucuronides"

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Oi, Naomi, Takashi Hashimoto, and Kazuki Kanazawa. "A Possible Mechanism That Flavonoids Exert Anticarcinogenesis with Activation of β-Glucuronidase in Cancerous Tissues." In ACS Symposium Series. American Chemical Society, 2008. http://dx.doi.org/10.1021/bk-2008-0993.ch010.

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Mol, J. N. M., R. E. Koes, R. van Blokland, et al. "The Potential Use of the Glucuronidase Reporter Gene and Antisense Technologies to Unravel Biological Functions of Flavonoids." In NATO ASI Series. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74158-6_6.

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Theja, Indireddy, and Banoth Ramya Kuber. "Recent Advances in Flavonoid Metabolism: An Updated Review." In Flavonoid Metabolism - Recent Advances and Applications in Crop Breeding [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.106243.

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Flavonoids are polyhydroxylated natural chemicals that have been shown to improve human health. These are a type of bioactive molecules that can be found in abundance in plants. These polyphenolic chemicals are naturally generated from plant metabolites. Before entering the intestine, flavonoid glycosides are deglycosylated, while aglycones can readily pass-through cell membranes. They are absorbed and transferred to the liver, where they undergo substantial metabolism, resulting in glucuronides, sulfates, and methylation compounds. These conjugates are responsible for the health-promoting possessions of flavonoids. The flavonol subclass was the first to be researched, with quercetin as the most common dietary flavonol, and information on other flavonoid subclasses is still developing. Cellular signaling pathways mediate the antidiabetic benefits of dietary flavonoids in the pancreas, liver, and skeletal muscle. Flavonoids modulate distinct signaling pathways in pancreatic cells, hepatocytes, adipocytes, and skeletal myofibers via acting on various molecular targets. Flavonoids may help people with diabetes firstly by improving hyperglycemia through glucose metabolism regulation in hepatocytes and secondly by reducing insulin resistance, inflammation, and oxidative stress in muscle and fat and by increasing glucose uptake in skeletal muscle and white adipose tissue. A greater understanding of the flavonoid pathway’s regulatory mechanisms would likely favor the progress of novel bioprocessing techniques for the production of value-added plants with optimal flavonoid content.
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Akinyinka Akinwumi, Kazeeem, Oluwole Olusoji Eleyowo, and Omolara Omowunmi Oladipo. "A Review on the Ethnobotanical Uses, Phytochemistry and Pharmacology Effect of Luffa cylindrica." In Pharmacognosy - Medicinal Plants [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.98405.

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Luffa cylindrica, popularly known as sponge gourd is a tropic and sub-tropical fibrous plant with fruits containing black seeds. The fruit is consumed by humans as a vegetable in many parts of Asia, while different parts of the plant are used for cosmetics and as medicine in many parts of the globe. The plant has been used in the treatment of many ailments including nose cancer, snake venom, wound healing, edema, enterobiasis, filaria, whooping cough, stomach upset, stomach pain and malaria. Many health-promoting compounds such as flavonoids (apigenin-7- glucuronide luteolin-7-O-β-D-glucuronide methyl ester, -O-feruloyl-β-D-glucose, luteolin-7-O-β-D-glucuronide methyl ester), phenolics acids (p-Coumaric, gallic, caffeic, chlorogenic), triterpenoids (oleanolic acid and echinocystic acid), saponins (Lucyoside A-M), tannins (catechin), ribosome-inactivating proteins (α- luffin), carotenoids (9 -cis neoxanthin, all-trans-lutein, all-trans-β-carotene), chlorophylls (chlorophyll a and b, pheophytin), cucurbitacin B and gypsogenin have been detected or isolated from different parts of the plants. Extracts of the plant and isolated compounds have wide spectrum pharmacological activities and have been shown to possess antiemetic, antidiabetic, antiviral, wound healing, anticancer, antipyretic, anti-inflammatory, antifungal, anti-bacteria, anthelmintic, hypoglycemic and antihyperglycemic, anti-inflammatory, antioxidant activity, and hepato-protective effects in animal models. However, further information is needed on its safety and mechanisms of action. The present article is an updated review of the ethnobotanical uses, pharmacological actions, phytochemistry, safety, and future application of Luffa cylindrica in translational medicine.
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