Artykuły w czasopismach na temat „QUERCETIN ANALOGUES”
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Otieno, Filex, i Richard Kagia. "Virtual screening for chemical analogues similar to phytochemicals that inhibit aldose reductase in the development of diabetic microvascular complications". F1000Research 12 (21.03.2023): 314. http://dx.doi.org/10.12688/f1000research.129663.1.
Pełny tekst źródłaPardo, Antonelle, Thomas Josse, Laetitia Mespouille, Bertrand Blankert, Philippe Dubois i Pierre Duez. "Synthesis of Quercetin-imprinted Polymer Spherical Particles with Improved Ability to Capture Quercetin Analogues". Phytochemical Analysis 28, nr 4 (26.01.2017): 289–96. http://dx.doi.org/10.1002/pca.2674.
Pełny tekst źródłaBiler, Michal, David Biedermann, Kateřina Valentová, Vladimír Křen i Martin Kubala. "Quercetin and its analogues: optical and acido–basic properties". Phys. Chem. Chem. Phys. 19, nr 39 (2017): 26870–79. http://dx.doi.org/10.1039/c7cp03845c.
Pełny tekst źródłaImai, Kohei, Ikuo Nakanishi, Kei Ohkubo, Yusuke Ohba, Takuya Arai, Mirei Mizuno, Shunichi Fukuzumi, Ken-ichiro Matsumoto i Kiyoshi Fukuhara. "Synthesis of methylated quercetin analogues for enhancement of radical-scavenging activity". RSC Advances 7, nr 29 (2017): 17968–79. http://dx.doi.org/10.1039/c7ra02329d.
Pełny tekst źródłaDuan, Yu, Na Sun, Min Xue, Xiaolan Wang i Hu Yang. "Synthesis of regioselectively acylated quercetin analogues with improved antiplatelet activity". Molecular Medicine Reports 16, nr 6 (12.10.2017): 9735–40. http://dx.doi.org/10.3892/mmr.2017.7781.
Pełny tekst źródłaFernández-Aparicio, Mónica, Marco Masi, Alessio Cimmino, Susana Vilariño i Antonio Evidente. "Allelopathic Effect of Quercetin, a Flavonoid from Fagopyrum esculentum Roots in the Radicle Growth of Phelipanche ramosa: Quercetin Natural and Semisynthetic Analogues Were Used for a Structure-Activity Relationship Investigation". Plants 10, nr 3 (13.03.2021): 543. http://dx.doi.org/10.3390/plants10030543.
Pełny tekst źródłaLitvin, V. A., i R. A. Njoh. "Quercetin as a precursor in the synthesis of analogues of fulvic acids and their antibacterial properties". Voprosy Khimii i Khimicheskoi Tekhnologii, nr 2 (marzec 2021): 56–64. http://dx.doi.org/10.32434/0321-4095-2021-135-2-56-64.
Pełny tekst źródłaAtala, Elias, Jocelyn Fuentes, Maria Jose Wehrhahn i Hernan Speisky. "Oxidation of Quercetin and Its Structural Analogues Differentially Affects Its Antioxidant Properties". Free Radical Biology and Medicine 100 (listopad 2016): S93. http://dx.doi.org/10.1016/j.freeradbiomed.2016.10.231.
Pełny tekst źródłaNayak, Yogendra, Venkatachalam Hillemane, Vijay Kumar Daroji, B. S. Jayashree i M. K. Unnikrishnan. "Antidiabetic Activity of Benzopyrone Analogues in Nicotinamide-Streptozotocin Induced Type 2 Diabetes in Rats". Scientific World Journal 2014 (2014): 1–12. http://dx.doi.org/10.1155/2014/854267.
Pełny tekst źródłaPrimikyri, Alexandra, Eleftheria Hatzimichael, Evdoxia Karali, Eleftherios Kostaras, Michalis Manztaris, Jae-Sun Shin, Seung-Wook Chi i in. "Decoding The BH3-Mimetic Pro-Apoptotic Activity Of Quercetin In Jurkat Cells". Blood 122, nr 21 (15.11.2013): 1672. http://dx.doi.org/10.1182/blood.v122.21.1672.1672.
Pełny tekst źródłaNör, Carolina, Ana Paula Machado Bernardi, Juliana Schulte Haas, Jan Schripsema, Sandra Beatriz Rech i Gilsane Lino Von Poser. "Phenolic Constituents of Hypericum Flowers". Natural Product Communications 3, nr 2 (luty 2008): 1934578X0800300. http://dx.doi.org/10.1177/1934578x0800300227.
Pełny tekst źródłaCoorssen, J. R. "Phospholipase activation and secretion: evidence that PLA2, PLC, and PLD are not essential to exocytosis". American Journal of Physiology-Cell Physiology 270, nr 4 (1.04.1996): C1153—C1163. http://dx.doi.org/10.1152/ajpcell.1996.270.4.c1153.
Pełny tekst źródłaSingh, Salam Pradeep, Rocktotpal Konwarh, Bolin Kumar Konwar i Niranjan Karak. "Molecular docking studies on analogues of quercetin with d-alanine:d-alanine ligase of Helicobacter pylori". Medicinal Chemistry Research 22, nr 5 (7.09.2012): 2139–50. http://dx.doi.org/10.1007/s00044-012-0207-7.
Pełny tekst źródłaTasdemir, Deniz, Marcel Kaiser, Reto Brun, Vanessa Yardley, Thomas J. Schmidt, Fatma Tosun i Peter Rüedi. "Antitrypanosomal and Antileishmanial Activities of Flavonoids and Their Analogues: In Vitro, In Vivo, Structure-Activity Relationship, and Quantitative Structure-Activity Relationship Studies". Antimicrobial Agents and Chemotherapy 50, nr 4 (kwiecień 2006): 1352–64. http://dx.doi.org/10.1128/aac.50.4.1352-1364.2006.
Pełny tekst źródłaJahangir, Muhammad, Atta-ur-Rehman, Ibrahim Bayoumi Abdel Farid, Robert Verpoorte, Imran Khan i Jiangnan Peng. "NMR-Based Metabolomics for Geographical Discrimination of Adhatoda vasica Leaves". Plants 12, nr 3 (18.01.2023): 453. http://dx.doi.org/10.3390/plants12030453.
Pełny tekst źródłaBiswas, Subhankar, Neetinkumar D. Reddy, B. S. Jayashree i C. Mallikarjuna Rao. "Evaluation of Novel 3-Hydroxyflavone Analogues as HDAC Inhibitors against Colorectal Cancer". Advances in Pharmacological Sciences 2018 (27.12.2018): 1–14. http://dx.doi.org/10.1155/2018/4751806.
Pełny tekst źródłaHossion, Abugafar M. L., Yoshito Zamami, Rafiya K. Kandahary, Tomofusa Tsuchiya, Wakano Ogawa, Akimasa Iwado i Kenji Sasaki. "Quercetin Diacylglycoside Analogues Showing Dual Inhibition of DNA Gyrase and Topoisomerase IV as Novel Antibacterial Agents". Journal of Medicinal Chemistry 54, nr 11 (9.06.2011): 3686–703. http://dx.doi.org/10.1021/jm200010x.
Pełny tekst źródłaCai, Weirong, Yong Chen, Liangliang Xie, Hong Zhang i Chunyuan Hou. "Characterization and density functional theory study of the antioxidant activity of quercetin and its sugar-containing analogues". European Food Research and Technology 238, nr 1 (14.09.2013): 121–28. http://dx.doi.org/10.1007/s00217-013-2091-x.
Pełny tekst źródłaDarko, Mitrović. "In silico analysis of molecular descriptors for quercetin analogues: a way to improve blood–brain barrier permeation". Intrinsic Activity 11, Suppl.1 (22.09.2023): A2.25. http://dx.doi.org/10.25006/ia.11.s1-a2.25.
Pełny tekst źródłaAdamus-Grabicka, Angelika A., Magdalena Markowicz-Piasecka, Marcin Cieślak, Karolina Królewska-Golińska, Paweł Hikisz, Joachim Kusz, Magdalena Małecka i Elzbieta Budzisz. "Biological Evaluation of 3-Benzylidenechromanones and Their Spiropyrazolines-Based Analogues". Molecules 25, nr 7 (1.04.2020): 1613. http://dx.doi.org/10.3390/molecules25071613.
Pełny tekst źródłaKondhare, Dasharath, Sushma Deshmukh i Harshad Lade. "Curcumin Analogues with Aldose Reductase Inhibitory Activity: Synthesis, Biological Evaluation, and Molecular Docking". Processes 7, nr 7 (2.07.2019): 417. http://dx.doi.org/10.3390/pr7070417.
Pełny tekst źródłaDe Sousa Lages, Adriana, Valentim Lopes, João Horta, João Espregueira-Mendes, Renato Andrade i Alexandre Rebelo-Marques. "Therapeutics That Can Potentially Replicate or Augment the Anti-Aging Effects of Physical Exercise". International Journal of Molecular Sciences 23, nr 17 (1.09.2022): 9957. http://dx.doi.org/10.3390/ijms23179957.
Pełny tekst źródłaRen, Yulin, Tyler Frank, Gunnar Meyer, Jizhou Lei, Jessica R. Grebenc, Ryan Slaughter, Yu G. Gao i A. Douglas Kinghorn. "Potential Benefits of Black Chokeberry (Aronia melanocarpa) Fruits and Their Constituents in Improving Human Health". Molecules 27, nr 22 (13.11.2022): 7823. http://dx.doi.org/10.3390/molecules27227823.
Pełny tekst źródłaBouktaib, Mohamed, Stéphane Lebrun, Aziz Atmani i Christian Rolando. "Hemisynthesis of all the O-monomethylated analogues of quercetin including the major metabolites, through selective protection of phenolic functions". Tetrahedron 58, nr 50 (grudzień 2002): 10001–9. http://dx.doi.org/10.1016/s0040-4020(02)01306-6.
Pełny tekst źródłaD.Bharathi, P. Valentina i N. Ramalakshmi. "MOLECULAR DOCKING OF NOVEL BENZOPYRAN ANALOGUES AND INHIBITION PROPERTIES OF ANTIDIABETIC AGENTS AGAINST α-AMYLASE AND αGLUCOSIDASE". RASAYAN Journal of Chemistry 15, nr 04 (2022): 2873–78. http://dx.doi.org/10.31788/rjc.2022.1547075.
Pełny tekst źródłaBurchinsky, S. G., i М. A. Kalinichenko. "Neurogeroprotection in neurological practice: new possibilities". Medicine of Ukraine, nr 2-3(258-259) (17.06.2022): 25–30. http://dx.doi.org/10.37987/1997-9894.2022.2-3(258-259).264051.
Pełny tekst źródłaBonaldo, Federico, Fulvio Mattivi, Daniele Catorci, Panagiotis Arapitsas i Graziano Guella. "H/D Exchange Processes in Flavonoids: Kinetics and Mechanistic Investigations". Molecules 26, nr 12 (10.06.2021): 3544. http://dx.doi.org/10.3390/molecules26123544.
Pełny tekst źródłaZhang, Jun-Sheng, Han-Zhuang Weng, Jia-Luo Huang, Gui-Hua Tang i Sheng Yin. "Anti-inflammatory Ingenane Diterpenoids from the Roots of Euphorbia kansui". Planta Medica 84, nr 18 (25.06.2018): 1334–39. http://dx.doi.org/10.1055/a-0646-4306.
Pełny tekst źródłaZou, Xiang-Yue, Ying-Jie He, Yi-Hui Yang, Xin-Pei Yan, Zhang-Bao Li i Hua Yang. "Systematic Identification of Bioactive Compositions in Leaves of Morus Cultivars Using UHPLC-ESI-QTOF-MS/MS and Comprehensive Screening of High-Quality Resources". Separations 9, nr 3 (15.03.2022): 76. http://dx.doi.org/10.3390/separations9030076.
Pełny tekst źródłaAbdizadeh, Tooba. "Efficacy Evaluation of Quercetin and Its Analogues on the Main Protease Enzyme of the COVID-19 Using Molecular Docking Studies". journal of ilam university of medical sciences 30, nr 4 (1.10.2022): 66–85. http://dx.doi.org/10.52547/sjimu.30.4.66.
Pełny tekst źródłaChen, Jih-Jung, Tzong-Huei Lee i Ming-Jen Cheng. "Secondary Metabolites with Anti-Inflammatory Activities from an Actinobacteria Herbidospora daliensis". Molecules 27, nr 6 (14.03.2022): 1887. http://dx.doi.org/10.3390/molecules27061887.
Pełny tekst źródłaThangasamy, Thilakavathy, Sivanandane Sittadjody, Kirsten H. Limesand i Randy Burd. "Tyrosinase Overexpression Promotes ATM-Dependent p53 Phosphorylation by Quercetin and Sensitizes Melanoma Cells to Dacarbazine". Analytical Cellular Pathology 30, nr 5 (1.01.2008): 371–87. http://dx.doi.org/10.1155/2008/764086.
Pełny tekst źródłaGanesh, Deepa, Hans-Peter Fuehrer, Peter Starzengrüber, Paul Swoboda, Wasif Ali Khan, Johannes A. B. Reismann, Milena S. K. Mueller, Peter Chiba i Harald Noedl. "Antiplasmodial activity of flavonol quercetin and its analogues in Plasmodium falciparum: evidence from clinical isolates in Bangladesh and standardized parasite clones". Parasitology Research 110, nr 6 (4.01.2012): 2289–95. http://dx.doi.org/10.1007/s00436-011-2763-z.
Pełny tekst źródłaVlasenko, Ludmila, i Kseniya Atlanderova. "Assessment (in vitro) toxicity of small molecules of plant origin". E3S Web of Conferences 390 (2023): 07022. http://dx.doi.org/10.1051/e3sconf/202339007022.
Pełny tekst źródłaMoalin, Mohamed, Gino P. F. van Strijdonck, Aalt Bast i Guido R. M. M. Haenen. "Competition between Ascorbate and Glutathione for the Oxidized Form of Methylated Quercetin Metabolites and Analogues: Tamarixetin, 4′O-Methylquercetin, Has the Lowest Thiol Reactivity". Journal of Agricultural and Food Chemistry 60, nr 36 (27.08.2012): 9292–97. http://dx.doi.org/10.1021/jf302068v.
Pełny tekst źródłaHladkykh, Feydor V. "Preventive and therapeutic strategies of pharmaco-correction gastropathy induced by nonsteroidal anti-inflammatory drugs". Reviews on Clinical Pharmacology and Drug Therapy 15, nr 4 (15.12.2017): 14–23. http://dx.doi.org/10.17816/rcf15414-23.
Pełny tekst źródłaAyoub, Zeenat, Archana Mehta i Siddhartha Kumar Mishra. "ETHNOPHARMACOLOGICAL REVIEW OF NATURAL PRODUCTS IN CANCER PREVENTION AND THERAPY". Asian Journal of Pharmaceutical and Clinical Research 11, nr 6 (7.06.2018): 32. http://dx.doi.org/10.22159/ajpcr.2018.v11i6.24792.
Pełny tekst źródłaMaya-Meraz, Irma Ofelia, José de Jesús Ornelas-Paz, Jaime David Pérez-Martínez, Alfonso A. Gardea-Béjar, Claudio Rios-Velasco, Saúl Ruiz-Cruz, Juan Ornelas-Paz, Ramona Pérez-Leal i José Juan Virgen-Ortiz. "Foliar Application of CaCO3-Rich Industrial Residues on ‘Shiraz’ Vines Improves the Composition of Phenolic Compounds in Grapes and Aged Wine". Foods 12, nr 8 (7.04.2023): 1566. http://dx.doi.org/10.3390/foods12081566.
Pełny tekst źródłaTorres-Piedra, Mariana, Rolffy Ortiz-Andrade, Rafael Villalobos-Molina, Narender Singh, Jose L. Medina-Franco, Scott P. Webster, Margaret Binnie, Gabriel Navarrete-Vázquez i Samuel Estrada-Soto. "A comparative study of flavonoid analogues on streptozotocin–nicotinamide induced diabetic rats: Quercetin as a potential antidiabetic agent acting via 11β-Hydroxysteroid dehydrogenase type 1 inhibition". European Journal of Medicinal Chemistry 45, nr 6 (czerwiec 2010): 2606–12. http://dx.doi.org/10.1016/j.ejmech.2010.02.049.
Pełny tekst źródłaBelchor, Mariana Novo, Caroline Ramos da Cruz Costa, Airam Roggero, Laila L. F. Moraes, Ricardo Samelo, Isabelly Annunciato, Marcos Antonio de Oliveira, Sergio F. Sousa i Marcos Hikari Toyama. "In Silico Evaluation of Quercetin Methylated Derivatives on the Interaction with Secretory Phospholipases A2 from Crotalus durissus terrificus and Bothrops jararacussu". Pharmaceuticals 16, nr 4 (15.04.2023): 597. http://dx.doi.org/10.3390/ph16040597.
Pełny tekst źródłaRiendeau, D., J. P. Falgueyret, J. Guay, N. Ueda i S. Yamamoto. "Pseudoperoxidase activity of 5-lipoxygenase stimulated by potent benzofuranol and N-hydroxyurea inhibitors of the lipoxygenase reaction". Biochemical Journal 274, nr 1 (15.02.1991): 287–92. http://dx.doi.org/10.1042/bj2740287.
Pełny tekst źródłaSzydłowska, Iwona, Jolanta Nawrocka-Rutkowska, Agnieszka Brodowska, Aleksandra Marciniak, Andrzej Starczewski i Małgorzata Szczuko. "Dietary Natural Compounds and Vitamins as Potential Cofactors in Uterine Fibroids Growth and Development". Nutrients 14, nr 4 (9.02.2022): 734. http://dx.doi.org/10.3390/nu14040734.
Pełny tekst źródłaKwofie, Samuel K., Kweku S. Enninful, Jaleel A. Yussif, Lina A. Asante, Mavis Adjei, Kwabena Kan-Dapaah, Elvis K. Tiburu i in. "Molecular Informatics Studies of the Iron-Dependent Regulator (ideR) Reveal Potential Novel Anti-Mycobacterium ulcerans Natural Product-Derived Compounds". Molecules 24, nr 12 (21.06.2019): 2299. http://dx.doi.org/10.3390/molecules24122299.
Pełny tekst źródłaGejalakshmi, S., i N. Harikrishnan. "Molecular Docking Study of Quercetein Analogues for Treating Tumours". International Journal of PharmTech Research 12, nr 4 (2019): 30–34. http://dx.doi.org/10.20902/ijptr.2019.120405.
Pełny tekst źródłaGao, Buhong, Yu Sun, Yingchun Miao, Li Xu i Zhongxia Wang. "Fluorometric detection of pH and quercetin based on nitrogen and phosphorus co-doped highly luminescent graphene-analogous flakes". Analyst 145, nr 1 (2020): 115–21. http://dx.doi.org/10.1039/c9an02077b.
Pełny tekst źródłaHabtemariam, Solomon. "α-Glucosidase Inhibitory Activity of Kaempferol-3-O-rutinoside". Natural Product Communications 6, nr 2 (luty 2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600211.
Pełny tekst źródłaNawwar, Mahmoud, Nahla Ayoub, Mohamed El-Raey, Soumaya Zaghloul, Amani Hashem, Eman Mostafa, Omayma Eldahshan, Ulrike Lindequist i Michael W. Linscheid. "Acylated flavonol diglucosides from Ammania auriculata". Zeitschrift für Naturforschung C 70, nr 1-2 (1.01.2015): 39–43. http://dx.doi.org/10.1515/znc-2014-4165.
Pełny tekst źródłaKamal, M. Vedant, G. Aadarsh Anand i Badal Parekh. "Antimicrobial activity of synthetic quercetin analogue on E. coli and S. aureus". Journal of Pharmacognosy and Phytochemistry 10, nr 5 (1.09.2021): 205–8. http://dx.doi.org/10.22271/phyto.2021.v10.i5c.14199.
Pełny tekst źródłaSpeisky, Hernán, María Fernanda Arias-Santé i Jocelyn Fuentes. "Oxidation of Quercetin and Kaempferol Markedly Amplifies Their Antioxidant, Cytoprotective, and Anti-Inflammatory Properties". Antioxidants 12, nr 1 (9.01.2023): 155. http://dx.doi.org/10.3390/antiox12010155.
Pełny tekst źródłaBraune, Annett, Michael Gütschow, Wolfram Engst i Michael Blaut. "Degradation of Quercetin and Luteolin byEubacterium ramulus". Applied and Environmental Microbiology 67, nr 12 (1.12.2001): 5558–67. http://dx.doi.org/10.1128/aem.67.12.5558-5567.2001.
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