Добірка наукової літератури з теми "Flavanol derivatives"
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Статті в журналах з теми "Flavanol derivatives"
Gómez-Juaristi, Miren, Beatriz Sarria, Sara Martínez-López, Laura Bravo Clemente, and Raquel Mateos. "Flavanol Bioavailability in Two Cocoa Products with Different Phenolic Content. A Comparative Study in Humans." Nutrients 11, no. 7 (June 26, 2019): 1441. http://dx.doi.org/10.3390/nu11071441.
Повний текст джерелаFan, Peihong, Hongxiang Lou, Wentao Yu, Dongmei Ren, Bin Ma, and Mei Ji. "Novel flavanol derivatives from grape seeds." Tetrahedron Letters 45, no. 15 (April 2004): 3163–66. http://dx.doi.org/10.1016/j.tetlet.2004.02.054.
Повний текст джерелаYang, Minghui, Le Cai, Xiaojing Shen, Mian Zhao, Tianpeng Yin, and Zhongtao Ding. "Two Unusual Flavanol Derivatives from Brainea insignis." Chinese Journal of Chemistry 30, no. 6 (June 2012): 1323–26. http://dx.doi.org/10.1002/cjoc.201200158.
Повний текст джерелаФедосеева (Fedoseeva), Людмила (Ljudmila) Михайловна (Mihajlovna), and Георгий (Georgij) Родионович (Rodionovich) Кутателадзе (Kutateladze). "STUDY OF SOME PHENOLIC COMPOUNDS OF THE COMMON SORREL AERAL PART, GROWING IN THE AL-TAI TERRITORY." chemistry of plant raw material, no. 4 (April 18, 2017): 91–96. http://dx.doi.org/10.14258/jcprm.2017041861.
Повний текст джерелаMottaghipisheh, Javad, and Marcello Iriti. "Sephadex® LH-20, Isolation, and Purification of Flavonoids from Plant Species: A Comprehensive Review." Molecules 25, no. 18 (September 10, 2020): 4146. http://dx.doi.org/10.3390/molecules25184146.
Повний текст джерелаVidal-Casanella, Oscar, Oscar Nuñez, and Javier Saurina. "Liquid Chromatographic Fingerprints for the Characterization of Flavanol-Rich Nutraceuticals Based on 4-Dimethylaminocinnamaldehyde Precolumn Derivatization." Scientia Pharmaceutica 89, no. 2 (May 6, 2021): 18. http://dx.doi.org/10.3390/scipharm89020018.
Повний текст джерелаSÁNCHEZ-ILÁRDUYA, M. B., C. SÁNCHEZ-FERNÁNDEZ, M. VILORIA-BERNAL, D. M. LÓPEZ-MÁRQUEZ, L. A. BERRUETA, B. GALLO, and F. VICENTE. "Mass spectrometry fragmentation pattern of coloured flavanol-anthocyanin and anthocyanin-flavanol derivatives in aged red wines of Rioja." Australian Journal of Grape and Wine Research 18, no. 2 (May 25, 2012): 203–14. http://dx.doi.org/10.1111/j.1755-0238.2012.00190.x.
Повний текст джерелаLi, Dong-Li, Xiao-Ming Li, Ze-Yu Peng, and Bin-Gui Wang. "Flavanol Derivatives from Rhizophora stylosa and Their DPPH Radical Scavenging Activity." Molecules 12, no. 5 (May 26, 2007): 1163–69. http://dx.doi.org/10.3390/12051163.
Повний текст джерелаAldrich, Leslie, Qiwen Gao, Lianyan Xu, Vincent Parise, and Yash Mehta. "Enantioselective Synthesis of 4-Amino-3-hydroxybenzopyran Flavanol Derivatives from Chalcones." Synthesis 50, no. 24 (November 21, 2018): 4796–808. http://dx.doi.org/10.1055/s-0037-161114.
Повний текст джерелаNawrot-Hadzik, Izabela, Adam Matkowski, Jakub Hadzik, Barbara Dobrowolska-Czopor, Cyprian Olchowy, Marzena Dominiak, and Paweł Kubasiewicz-Ross. "Proanthocyanidins and Flavan-3-Ols in the Prevention and Treatment of Periodontitis—Antibacterial Effects." Nutrients 13, no. 1 (January 7, 2021): 165. http://dx.doi.org/10.3390/nu13010165.
Повний текст джерелаДисертації з теми "Flavanol derivatives"
方顥伶. "One-Pot Synthesis of Bioactive Decahydroquinolines and Flavanone Derivatives Using Iodine as Catalyst." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/10554964013312880949.
Повний текст джерелаChiou, Yi-Ling, and 邱翊玲. "Effects of flavanone derivatives and fenofibrate on melanogenesis in murine B16-F10 melanoma cells." Thesis, 2009. http://ndltd.ncl.edu.tw/handle/38776993419825850819.
Повний текст джерела靜宜大學
化粧品科學系碩士班
98
The color of mammalian skin and hair is determined by a number of factors, the most obvious phenotypical characteristics of which is the distribution of melanin pigment. Therefore, melanocytes act as important regulators for skin pigmentation and targets to study the mechanism of melanoma. In the present study, we investigated the action mechanisms of Citrus flavonoids and peroxisome proliferator-activated receptors (PPARs) activators on melanogenesis in B16-F10 melanoma cells. The most abundant Citrus flavonoids are flavanones, such as naringenin, naringin, narirutin, hesperetin, hesperidin and neohesperidin. We showed that the synthesis of melanin was strongly increased by naringrnin or hesperetin, the flavanone aglycone. In this study, the cellular tyrosinase activity also enhanced by naringenin in a concentration-dependent manner. Moreover, naringenin increased the intracellular cAMP level and the naringenin-induced melanogenesis was completely abolished by H89, an inhibitor of protein kinase A. Furthermore, we determined the roles of mitogen-activated protein kinases (MAPKs) on naringenin-induced melanogenesis. The melanin contents of naringenin-treated cells were significantly raised by the addition of U0126 and LY294002, an inhibitor of MAPK kinase and phosphatidylinositol 3-kinase (PI3K), respectively. These results suggest that naringenin increases melanin synthesis through a cAMP-dependent mechanism and probably via the modulation of MAPK or PI3K pathway. PPARs (peroxisome proliferator-activated receptors) are members of the nuclear hormone receptor superfamily. Agonists of PPARs have been known to play an important role in epidermis homeostasis. However, the molecular events of PPARs have not been well investigated in melanocytes. We evaluated the effects of PPAR agonists on the melanogenic activities. The data showed that only the PPARα activator (fenofibrate) significantly inhibited the melanin synthesis, not PPARβ activator (GW0742) or PPARγ activator (ciglitazone). In addition, fenofibrate also diminished the expression of MITF but did not alter the cellular tyrosinase activity. The present study implies that PPARα activator reduces melanin synthesis via the down-regulation of MITF in B16-F10 melanoma cells. PPARα may contribute to the regulation of melanogenesis.
Passreiter, C. M., A.-K. Suckow-Schnitker, A. Kulawik, Jonathan A. Addae-Kyereme, Colin W. Wright, and W. Wätjen. "Prenylated flavanone derivatives isolated from Erythrina addisoniae are potent inducers of apoptotic cell death." 2015. http://hdl.handle.net/10454/7498.
Повний текст джерелаExtracts of Erythrina addisoniae are frequently used in the traditional medicine of Western Africa, but insufficient information about active compounds is available. From the stem bark of E. addisoniae, three (1, 2, 4) and three known (3, 5, 6) flavanones were isolated: addisoniaflavanones I and II, containing either a 2″,3″-epoxyprenyl moiety (1) or a 2″,3″-dihydroxyprenyl moiety (2) were shown to be highly toxic (MTT assay: EC50 values of 5.25 ± 0.7 and 8.5 ± 1.3 μM, respectively) to H4IIE hepatoma cells. The cytotoxic potential of the other isolated flavanones was weaker (range of EC50 values between 15 and >100 μM). Toxic effects of addisoniaflavanone I and II were detectable after 3 h (MTT assay). Both compounds induced an apoptotic cell death (caspase-3/7 activation, nuclear fragmentation) in the hepatoma cells and, at high concentrations, also necrosis (membrane disruption: ethidium bromide staining). Formation of DNA strand breaks was not detectable after incubation with these compounds (comet assay). In conclusion, the prenylated flavanones addisoniaflavanones I and II may be of interest for pharmacological purposes due to their high cytotoxic and pro-apoptotic potential against hepatoma cells.
Liao, Wei-Ting, and 廖唯廷. "Synthesis of Flavanone Derivatives via Conjugate Addition of Chromones and Arylboronic Acids by Reusable Palladium Catalyst in Water." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/xh89a3.
Повний текст джерела國立臺北科技大學
有機高分子研究所
105
Flavonoids and flavanones are privileged structural motifs in numerous nature products and pharmaceutical molecules that show a variety of biological activities. For example: anti-oxidation, anti-inflammatory, anti-bacterial, anti-cancer and so on. In this study, we developed a Pd(OAc)2/cationic 2,2’-bipyridyl-catalytic system to catalyzed conjugate addition of chromones and arylboronic acids forming flavanone derivatives using water as the reaction medium. In comparison with other published conditions, our reaction not only use water as the green solvent for the further reuse studies but achieve excellent selectivity and good to excellent yields under low catalyst loading.
Частини книг з теми "Flavanol derivatives"
D’Ascenzio, Melissa. "The Role of Flavonoids and other Selected (Poly) Phenols in Cancer Prevention and Therapy: A Focus on Epigenetics." In Flavonoids and Phenolics, 384–489. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815079098122010015.
Повний текст джерелаEshghi, Hossein, Mahsa Khoshnevis, and Fatemeh Pirani. "Recent Progress on Natural and Synthetic Flavanone and its Derivatives." In Frontiers in Natural Product Chemistry: Volume 9, 185–256. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815040586122090009.
Повний текст джерелаТези доповідей конференцій з теми "Flavanol derivatives"
Šaćirović, Sabina, Andrija Ćirić, Mališa Antić, and Zoran Marković. "HPLC ANALYSIS OF PHENOLS OF SLOVENIAN RED WINES: CABERNET SAUVIGNON AND MERLOT." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.165s.
Повний текст джерелаPeng, Han, and Fereidoon Shahidi. "Antioxidant activity of EGC (epigallocatechin) ester derivatives in food and biological model system." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/qchb4629.
Повний текст джерела