Статті в журналах з теми "Flavanol derivatives"
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Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Flavanol derivatives".
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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 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 джерелаTorres, J. L., and R. Bobet. "New Flavanol Derivatives from Grape (Vitis vinifera) Byproducts. Antioxidant Aminoethylthio−Flavan-3-ol Conjugates from a Polymeric Waste Fraction Used as a Source of Flavanols." Journal of Agricultural and Food Chemistry 49, no. 10 (October 2001): 4627–34. http://dx.doi.org/10.1021/jf010368v.
Повний текст джерелаLi, Feng, Suresh Awale, Yasuhiro Tezuka, and Shigetoshi Kadota. "Cytotoxicity of Constituents from Mexican Propolis against a Panel of Six Different Cancer Cell Lines." Natural Product Communications 5, no. 10 (October 2010): 1934578X1000501. http://dx.doi.org/10.1177/1934578x1000501018.
Повний текст джерелаHuang, Deng-Ming, Hui-Jing Li, Yan Zhao, and Yan-Chao Wu. "Synthesis of Bisflavanol-Type Natural Products and Their Analogues via Self-Coupling of C8-Methylol Catechin Derivatives." Synthesis 51, no. 16 (April 24, 2019): 3127–41. http://dx.doi.org/10.1055/s-0037-1610707.
Повний текст джерелаPrat-García, Samanta, Joana Oliveira, Maria del Alamo-Sanza, Victor de Freitas, Ignacio Nevares, and Nuno Mateus. "Characterization of Anthocyanins and Anthocyanin-Derivatives in Red Wines during Ageing in Custom Oxygenation Oak Wood Barrels." Molecules 26, no. 1 (December 25, 2020): 64. http://dx.doi.org/10.3390/molecules26010064.
Повний текст джерелаRío Segade, Susana, Ignacio Orriols, Vincenzo Gerbi, and Luca Rolle. "Phenolic characterization of thirteen red grape cultivars from Galicia by anthocyanin profile and flavanol composition." OENO One 43, no. 4 (December 31, 2009): 189. http://dx.doi.org/10.20870/oeno-one.2009.43.4.791.
Повний текст джерелаOrabi, Mohamed A. A., Omaish Salman Alqahtani, Bandar A. Alyami, Ahmed Abdullah Al Awadh, El-Shaymaa Abdel-Sattar, Katsuyoshi Matsunami, Dalia I. Hamdan, and Mohamed E. Abouelela. "Human Lung Cancer (A549) Cell Line Cytotoxicity and Anti-Leishmania major Activity of Carissa macrocarpa Leaves: A Study Supported by UPLC-ESI-MS/MS Metabolites Profiling and Molecular Docking." Pharmaceuticals 15, no. 12 (December 14, 2022): 1561. http://dx.doi.org/10.3390/ph15121561.
Повний текст джерелаLuo, Yu, Yuqing Jian, Yingkai Liu, Sai Jiang, Daniyal Muhammad, and Wei Wang. "Flavanols from Nature: A Phytochemistry and Biological Activity Review." Molecules 27, no. 3 (January 22, 2022): 719. http://dx.doi.org/10.3390/molecules27030719.
Повний текст джерелаAFIFY, Abd El-Moneim M. R., Emad A. SHALABY, and Hossam Saad EL-BELTAGI. "Antioxidant Activity of Aqueous Extracts of Different Caffeine Products." Notulae Botanicae Horti Agrobotanici Cluj-Napoca 39, no. 2 (November 21, 2011): 117. http://dx.doi.org/10.15835/nbha3926254.
Повний текст джерелаSánchez-Ilárduya, María Belén, Cristina Sánchez-Fernández, Sergio Garmón-Lobato, Beatriz Abad-García, Luis Angel Berrueta, Blanca Gallo, and Francisca Vicente. "Detection of non-coloured anthocyanin–flavanol derivatives in Rioja aged red wines by liquid chromatography–mass spectrometry." Talanta 121 (April 2014): 81–88. http://dx.doi.org/10.1016/j.talanta.2013.12.066.
Повний текст джерелаDESRUES, OLIVIER, CHRISTOS FRYGANAS, HONORATA M. ROPIAK, IRENE MUELLER-HARVEY, HEIDI L. ENEMARK, and STIG M. THAMSBORG. "Impact of chemical structure of flavanol monomers and condensed tannins on in vitro anthelmintic activity against bovine nematodes." Parasitology 143, no. 4 (February 18, 2016): 444–54. http://dx.doi.org/10.1017/s0031182015001912.
Повний текст джерелаItnawita, Itnawita, Zamri Adel, Ganis Fia Kartika, Sofia Anita, T. Abu Hanifah, G. A. Guntur, and U. Shyfaa. "Use of the compound (2-(4-chlorophenyl)-3-hydroxy-4H-chromene-4-one) as a ligand complex formation by copper (II)." Current Chemistry Letters 11, no. 4 (2022): 353–58. http://dx.doi.org/10.5267/j.ccl.2022.6.002.
Повний текст джерелаLutfian, Lutfian, Aris Munandar, Rismawan Adi Yunanto та Ahmad Rizki Nur Hakiki. "Effectiveness of Yoga, Fast of Dawood, Green Tea and Apple Juice as Suppressors of PPAR-γ, C/EBP-α, and SREBP-c for Management of Obesity on Adolescents". Nursing and Health Sciences Journal (NHSJ) 1, № 3 (29 грудня 2021): 223–30. http://dx.doi.org/10.53713/nhs.v1i3.79.
Повний текст джерелаOktavianawati, Ika, Sattya Arimurti, and Suharjono Suharjono. "The Impacts of Traditional Fermentation Method on the Chemical Characteristics of Arabica Coffee Beans from Bondowoso District, East Java." Journal of Pure and Applied Chemistry Research 9, no. 2 (August 31, 2020): 133–41. http://dx.doi.org/10.21776/ub.jpacr.2020.009.02.526.
Повний текст джерелаIsmiyarto, Ismiyarto, Sabirin Matsjeh, and Chairil Anwar. "Synthesis of Chalcone and Flavanone Compound Using Raw Material of Acetophenone and Benzaldehyde Derivative." Indonesian Journal of Chemistry 1, no. 2 (June 3, 2010): 81–89. http://dx.doi.org/10.22146/ijc.21948.
Повний текст джерелаUrpi-Sarda, Mireia, Emma Ramiro-Puig, Nasiruddin Khan, Sara Ramos-Romero, Rafael Llorach, Margarida Castell, Susana Gonzalez-Manzano, Celestino Santos-Buelga, and Cristina Andres-Lacueva. "Distribution of epicatechin metabolites in lymphoid tissues and testes of young rats with a cocoa-enriched diet." British Journal of Nutrition 103, no. 10 (January 26, 2010): 1393–97. http://dx.doi.org/10.1017/s0007114509993473.
Повний текст джерелаTistechok, Stepan, Marc Stierhof, Anna Kachor, Maksym Myronovskyi, Oleksandr Gromyko та Andriy Luzhetskyy. "Flavacol and Its Novel Derivative 3-β-Hydroxy Flavacol from Streptomyces sp. Pv 4-95 after the Expression of Heterologous AdpA". Microorganisms 10, № 12 (25 листопада 2022): 2335. http://dx.doi.org/10.3390/microorganisms10122335.
Повний текст джерелаVargas-Arana, Gabriel, Claudia Merino-Zegarra, Ángel Martín Rodríguez del-Castillo, Cristina Quispe, Ezequiel Viveros-Valdez, and Mario J. Simirgiotis. "Antioxidant, Antiproliferative and Anti-Enzymatic Capacities, Nutritional Analysis and UHPLC-PDA-MS Characterization of Ungurahui Palm Fruits (Oenocarpus bataua Mart) from the Peruvian Amazon." Antioxidants 11, no. 8 (August 18, 2022): 1598. http://dx.doi.org/10.3390/antiox11081598.
Повний текст джерелаMardjan, Muhammad Idham Darussalam, Retno Ambarwati, Sabirin Matsjeh, Tutik Dwi Wahyuningsih, and Winarto Haryadi. "SYNTHESIS OF FLAVANONE-6-CARBOXYLIC ACID DERIVATIVES FROM SALICYLIC ACID DERIVATIVE." Indonesian Journal of Chemistry 12, no. 1 (February 14, 2012): 70–76. http://dx.doi.org/10.22146/ijc.21374.
Повний текст джерелаValkovska, Valda, and Liāna Orola. "Characterization of Pigments from <i>Malus domestica</i> Leaves for Wool Dyeing." Key Engineering Materials 903 (November 10, 2021): 63–68. http://dx.doi.org/10.4028/www.scientific.net/kem.903.63.
Повний текст джерелаKobori, Ryo, Syuichi Yakami, Takashi Kawasaki, and Akiko Saito. "Changes in the Polyphenol Content of Red Raspberry Fruits during Ripening." Horticulturae 7, no. 12 (December 10, 2021): 569. http://dx.doi.org/10.3390/horticulturae7120569.
Повний текст джерелаŠuković, Danijela, Bojana Knežević, Uroš Gašić, Milica Sredojević, Ivanka Ćirić, Slavica Todić, Jelena Mutić, and Živoslav Tešić. "Phenolic Profiles of Leaves, Grapes and Wine of Grapevine Variety Vranac (Vitis vinifera L.) from Montenegro." Foods 9, no. 2 (January 28, 2020): 138. http://dx.doi.org/10.3390/foods9020138.
Повний текст джерелаSong, Lijun, Jie Zheng, Li Zhang, Shijuan Yan, Wenjie Huang, Jun He, and Pengzhan Liu. "Phytochemical Profiling and Fingerprint Analysis of Chinese Jujube (Ziziphus jujuba Mill.) Leaves of 66 Cultivars from Xinjiang Province." Molecules 24, no. 24 (December 11, 2019): 4528. http://dx.doi.org/10.3390/molecules24244528.
Повний текст джерелаOffor, Benedict C., Msizi I. Mhlongo, Paul A. Steenkamp, Ian A. Dubery, and Lizelle A. Piater. "Untargeted Metabolomics Profiling of Arabidopsis WT, lbr-2-2 and bak1-4 Mutants Following Treatment with Two LPS Chemotypes." Metabolites 12, no. 5 (April 22, 2022): 379. http://dx.doi.org/10.3390/metabo12050379.
Повний текст джерелаOganesyan, Eduard T., та Stanislav S. Shatokhin. "USING QUANTUM-CHEMICAL PARAMETERS FOR PREDICTING ANTI-RADICAL (НО∙) ACTIVITY OF RELATED STRUCTURES CONTAINING A CINNAMOYL FRAGMENT II. DERIVATIVES OF 2’,4’-DIHYDROXYCHALCONE, FLAVANONE AND FLAVONE, CONTAINING A HYDROXY GROUP IN POSITION 7". Pharmacy & Pharmacology 8, № 2 (14 жовтня 2020): 112–23. http://dx.doi.org/10.19163/2307-9266-2020-8-2-112-123.
Повний текст джерелаYan-Nan, He, Ning Peng-Fei, Yue Tai-Xin, and Zhang Zhen-Wen. "Comparing phenolic composition of Cabernet Gernischet wines between rain-shelter cultivation and open-field cultivation." Czech Journal of Food Sciences 34, No. 3 (June 17, 2016): 254–70. http://dx.doi.org/10.17221/429/2015-cjfs.
Повний текст джерелаMaciel Diogo, Gabriela, Josimara Souza Andrade, Policarpo Ademar Sales Junior, Silvane Maria Fonseca Murta, Viviane Martins Rebello Dos Santos, and Jason Guy Taylor. "Trypanocidal Activity of Flavanone Derivatives." Molecules 25, no. 2 (January 17, 2020): 397. http://dx.doi.org/10.3390/molecules25020397.
Повний текст джерелаSyah, Yana M., and Emilio L. Ghisalberti. "Flavanone derivatives from Macaranga tanarius." Biochemical Systematics and Ecology 62 (October 2015): 151–54. http://dx.doi.org/10.1016/j.bse.2015.08.009.
Повний текст джерелаStec, Katarzyna, Joanna Kozłowska, Anna Wróblewska-Kurdyk, Bożena Kordan, Mirosław Anioł, and Beata Gabryś. "Effect of Naringenin and Its Derivatives on the Probing Behavior of Myzus persicae (Sulz.)." Molecules 25, no. 14 (July 13, 2020): 3185. http://dx.doi.org/10.3390/molecules25143185.
Повний текст джерелаChand, Karam, Amir Nasrolahi Shirazi, Preeti Yadav, Rakesh K. Tiwari, Meena Kumari, Keykavous Parang, and Sunil K. Sharma. "Synthesis and antiproliferative and c-Src kinase inhibitory activities of cinnamoyl- and pyranochromen-2-one derivatives." Canadian Journal of Chemistry 91, no. 8 (August 2013): 741–54. http://dx.doi.org/10.1139/cjc-2013-0053.
Повний текст джерелаSykuła, Anna, Agnieszka Kowalska-Baron, Krystian Gałęcki, Paulina Błazińska, and Elżbieta Łodyga-Chruścińska. "Structural and Spectral Investigation of a Series of Flavanone Derivatives." Molecules 26, no. 5 (February 28, 2021): 1298. http://dx.doi.org/10.3390/molecules26051298.
Повний текст джерелаHsu, Feng-Lin, Yan-Jyu Tsai, Mei-Chuan Kao, and Chieh-Fu Chen. "Antihepatotoxic Activity of Phenolic Flavan-3-ols and Their Derivatives." American Journal of Chinese Medicine 21, no. 01 (January 1993): 45–50. http://dx.doi.org/10.1142/s0192415x93000066.
Повний текст джерелаWang, Enhua, Lishou Yang, Qian Yang, Fanghong Yang, Ji Luo, Menglan Gan, Xue Wang, Shanmin Song, Yang Lei, and Xiaosheng Yang. "Polyphosphoric acid-promoted one-pot synthesis and neuroprotective effects of flavanones against NMDA-induced injury in PC12 cells." RSC Advances 12, no. 43 (2022): 28098–103. http://dx.doi.org/10.1039/d2ra03562f.
Повний текст джерелаConidi, Egea-Corbacho, and Cassano. "A Combination of Aqueous Extraction and Polymeric Membranes as a Sustainable Process for the Recovery of Polyphenols from Olive Mill Solid Wastes." Polymers 11, no. 11 (November 12, 2019): 1868. http://dx.doi.org/10.3390/polym11111868.
Повний текст джерелаChen, R. C., G. B. Sun, J. Wang, H. J. Zhang, and X. B. Sun. "Naringin protects against anoxia/reoxygenation-induced apoptosis in H9c2 cells via the Nrf2 signaling pathway." Food & Function 6, no. 4 (2015): 1331–44. http://dx.doi.org/10.1039/c4fo01164c.
Повний текст джерелаSinyeue, Cynthia, Mariko Matsui, Michael Oelgemöller, Frédérique Bregier, Vincent Chaleix, Vincent Sol, and Nicolas Lebouvier. "Synthesis and Investigation of Flavanone Derivatives as Potential New Anti-Inflammatory Agents." Molecules 27, no. 6 (March 9, 2022): 1781. http://dx.doi.org/10.3390/molecules27061781.
Повний текст джерелаFu, X., T. Sévenet, F. Remy, M. Païs, A. Hamid A. Hadi, and L. M. Zeng. "Flavanone and Chalcone Derivatives from Cryptocarya kurzii." Journal of Natural Products 56, no. 7 (July 1993): 1153–63. http://dx.doi.org/10.1021/np50097a021.
Повний текст джерелаShi, Lei, Xiu E. Feng, Jing Rong Cui, Lian Hua Fang, Guan Hua Du, and Qing Shan Li. "Synthesis and biological activity of flavanone derivatives." Bioorganic & Medicinal Chemistry Letters 20, no. 18 (September 2010): 5466–68. http://dx.doi.org/10.1016/j.bmcl.2010.07.090.
Повний текст джерелаZheng, Xu Xu, Jing Jing Xie, Zhong Yi Yin, and Jia Jia Jing. "A Simple Method of Cyclization of the 2'-Hydroxychalcone with Polystyrene-Pyridine Resine under Mild Conditions." Advanced Materials Research 295-297 (July 2011): 1156–59. http://dx.doi.org/10.4028/www.scientific.net/amr.295-297.1156.
Повний текст джерелаMphahlele, Malose J. "ChemInform Abstract: Schmidt Reaction of Flavanone Derivatives: Synthesis of Benzoheterazepine Derivatives." ChemInform 42, no. 21 (April 28, 2011): no. http://dx.doi.org/10.1002/chin.201121212.
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