Artículos de revistas sobre el tema "Anthraquinone"
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Drummond, Christopher A., Maria Teresa Molina, Sandra Taliansky, Carl R. Breidenbach y Carmen F. Fioravanti. "Effects of Quinizarin and Five Synthesized Derivatives on Fifth Larval Instar Midgut Ecdysone 20-Monooxygenase Activity of the Tobacco HornwormManduca sexta". International Journal of Zoology 2014 (2014): 1–8. http://dx.doi.org/10.1155/2014/261512.
Texto completoMalak, Lourin G., Daoud W. Bishay, Afaf M. Abdel-Baky, Ahmed M. Moharram, Stephen J. Cutler y Samir A. Ross. "New Anthraquinone Derivatives from Geosmithia lavendula". Natural Product Communications 8, n.º 2 (febrero de 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800215.
Texto completoGao, Huiyu, Jianbo Yang, Xueting Wang, Yunfei Song, Xianlong Cheng, Feng Wei, Ying Wang, Donglin Gu, Hua Sun y Shuangcheng Ma. "Exploratory Quality Control Study for Polygonum multiflorum Thunb. Using Dinuclear Anthraquinones with Potential Hepatotoxicity". Molecules 27, n.º 19 (10 de octubre de 2022): 6760. http://dx.doi.org/10.3390/molecules27196760.
Texto completoBranco, Alexsandro, Angelo C. Pinto, Jan Schripsema y Raimundo Braz-Filho. "Anthraquinones from the bark of Senna macranthera". Anais da Academia Brasileira de Ciências 83, n.º 4 (diciembre de 2011): 1159–64. http://dx.doi.org/10.1590/s0001-37652011000400003.
Texto completoZhang, Rongfei, Yuanyuan Miao, Lingyun Chen, Shanyong Yi y Ninghua Tan. "De Novo Transcriptome Analysis Reveals Putative Genes Involved in Anthraquinone Biosynthesis in Rubia yunnanensis". Genes 13, n.º 3 (16 de marzo de 2022): 521. http://dx.doi.org/10.3390/genes13030521.
Texto completoUllah, Hossain, Junhyeong Kim, Naveed Rehman, Hye-Jin Kim, Mi-Jeong Ahn y Hye Chung. "A Simple and Sensitive Liquid Chromatography with Tandem Mass Spectrometric Method for the Simultaneous Determination of Anthraquinone Glycosides and Their Aglycones in Rat Plasma: Application to a Pharmacokinetic Study of Rumex acetosa Extract". Pharmaceutics 10, n.º 3 (20 de julio de 2018): 100. http://dx.doi.org/10.3390/pharmaceutics10030100.
Texto completoYang, Yong, Qiao-Xia Wu y Min Xue. "Bifurcated hydrogen bonding mediated planar 9,10-anthraquinone dyes: synthesis, structure and properties". RSC Advances 5, n.º 37 (2015): 28932–37. http://dx.doi.org/10.1039/c5ra01682g.
Texto completoManojlovic, N. T., S. Solujic, S. Sukdolak y Lj Krstic. "Isolation and antimicrobial activity of anthraquinones from some species of the lichen genus Xanthoria". Journal of the Serbian Chemical Society 65, n.º 8 (2000): 555–60. http://dx.doi.org/10.2298/jsc0008555m.
Texto completoAmmar Rushdan, Nur Afiqah Nadhiah, Nurunajah Ab Ghani y Nurulfazlina Edayah Rasol. "Review on Anthraquinones Isolated from Rubiaceae Family". Journal of Science and Mathematics Letters 11, Special (9 de noviembre de 2023): 163–74. http://dx.doi.org/10.37134/jsml.vol11.sp.18.2023.
Texto completoHafez Ghoran, Salar, Fatemeh Taktaz, Seyed Abdulmajid Ayatollahi y Anake Kijjoa. "Anthraquinones and Their Analogues from Marine-Derived Fungi: Chemistry and Biological Activities". Marine Drugs 20, n.º 8 (25 de julio de 2022): 474. http://dx.doi.org/10.3390/md20080474.
Texto completoGriffiths, Scott, Carl H. Mesarich, Benedetta Saccomanno, Abraham Vaisberg, Pierre J. G. M. De Wit, Russell Cox y Jérôme Collemare. "Elucidation of cladofulvin biosynthesis reveals a cytochrome P450 monooxygenase required for anthraquinone dimerization". Proceedings of the National Academy of Sciences 113, n.º 25 (6 de junio de 2016): 6851–56. http://dx.doi.org/10.1073/pnas.1603528113.
Texto completoHynninen, Paavo H., Riikka Räisänen, Pia Elovaara y Eila Nokelainen. "Preparative Isolation of Anthraquinones from the Fungus Dermocybe sanguined Using Enzymatic Hydrolysis by the Endogenous β-Glucosidase". Zeitschrift für Naturforschung C 55, n.º 7-8 (1 de agosto de 2000): 600–610. http://dx.doi.org/10.1515/znc-2000-7-820.
Texto completoAnderson, Benjamin R. y Mark G. Kuzyk. "Imaging studies of photodegradation and self-healing in anthraquinone derivative dye-doped PMMA". Physical Chemistry Chemical Physics 22, n.º 48 (2020): 28154–64. http://dx.doi.org/10.1039/d0cp05426g.
Texto completoPark, Jae Gwang, Seung Cheol Kim, Yun Hwan Kim, Woo Seok Yang, Yong Kim, Sungyoul Hong, Kyung-Hee Kim et al. "Anti-Inflammatory and Antinociceptive Activities of Anthraquinone-2-Carboxylic Acid". Mediators of Inflammation 2016 (2016): 1–12. http://dx.doi.org/10.1155/2016/1903849.
Texto completoSadiq, Uzma, Fatima Shahid, Harsharn Gill y Jayani Chandrapala. "The Release Behavior of Anthraquinones Encapsulated into Casein Micelles during In Vitro Digestion". Foods 12, n.º 15 (27 de julio de 2023): 2844. http://dx.doi.org/10.3390/foods12152844.
Texto completoLyčka, Antonín, Libuše Havlíčková, Alois Koloničný y Josef Jirman. "15N NMR study of amino-imino tautomerism in derivatives of 1,4-bis(substituted amino)-9,10-anthraquinones and 1,4-bis(substituted amino)-2,3-dihydro-9,10-anthraquinones". Collection of Czechoslovak Chemical Communications 52, n.º 3 (1987): 736–41. http://dx.doi.org/10.1135/cccc19870736.
Texto completoBoniface, PJ, RC Cambie, C. Higgs, PS Rutledge y PD Woodgate. "Experiments Directed Towards the Synthesis of Anthracyclinones. XXVII. Transformations of 2,3-Bisalkynyl and 2,3-Bisalkenyl Anthraquinones". Australian Journal of Chemistry 48, n.º 6 (1995): 1089. http://dx.doi.org/10.1071/ch9951089.
Texto completoLaub, Annegret, Ann-Katrin Sendatzki, Götz Palfner, Ludger A. Wessjohann, Jürgen Schmidt y Norbert Arnold. "HPTLC-DESI-HRMS-Based Profiling of Anthraquinones in Complex Mixtures—A Proof-of-Concept Study Using Crude Extracts of Chilean Mushrooms". Foods 9, n.º 2 (6 de febrero de 2020): 156. http://dx.doi.org/10.3390/foods9020156.
Texto completoBussmann, Rainer W., Lothar Hennig, Athanassios Giannis, Jutta Ortwein, Toni M. Kutchan y Xi Feng. "Anthraquinone Content in Noni (Morinda citrifoliaL.)". Evidence-Based Complementary and Alternative Medicine 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/208378.
Texto completoLi, Rong-Rong, Xue-Fang Liu, Su-Xiang Feng, Sheng-Nan Shu, Pei-Yang Wang, Na Zhang, Jian-Sheng Li y Ling-Bo Qu. "Pharmacodynamics of Five Anthraquinones (Aloe-emodin, Emodin, Rhein, Chysophanol, and Physcion) and Reciprocal Pharmacokinetic Interaction in Rats with Cerebral Ischemia". Molecules 24, n.º 10 (17 de mayo de 2019): 1898. http://dx.doi.org/10.3390/molecules24101898.
Texto completoOsman, Che Puteh y Nor Hadiani Ismail. "A REVIEW ON THE CHEMISTRY AND PHARMACOLOGY OF Rennellia elliptica Korth". Indonesian Journal of Tropical and Infectious Disease 6, n.º 6 (21 de diciembre de 2017): 131. http://dx.doi.org/10.20473/ijtid.v6i6.6642.
Texto completoChee, Cheok Wui, Nor Hisam Zamakshshari, Vannajan Sanghiran Lee, Iskandar Abdullah, Rozana Othman, Yean Kee Lee, Najihah Mohd Hashim y Nurshamimi Nor Rashid. "Morindone from Morinda citrifolia as a potential antiproliferative agent against colorectal cancer cell lines". PLOS ONE 17, n.º 7 (12 de julio de 2022): e0270970. http://dx.doi.org/10.1371/journal.pone.0270970.
Texto completoHung, Hsin-Yi, Kun-Ching Cheng, Ping-Chung Kuo, I.-Tsen Chen, Yue-Chiun Li, Tsong-Long Hwang, Sio-Hong Lam y Tian-Shung Wu. "Chemical Constituents of Hedyotis diffusa and Their Anti-Inflammatory Bioactivities". Antioxidants 11, n.º 2 (9 de febrero de 2022): 335. http://dx.doi.org/10.3390/antiox11020335.
Texto completoKunze, Arno, Ludger Witte, Manuel Aregullin, Eloy Rodriguez y Peter Proksch. "Anthraquinones in the Leaf Beetle Trirhabda geminata (Chrysomelidae)". Zeitschrift für Naturforschung C 51, n.º 3-4 (1 de abril de 1996): 249–52. http://dx.doi.org/10.1515/znc-1996-3-417.
Texto completoSadiq, Uzma, Harsharn Gill, Jayani Chandrapala y Fatima Shahid. "Influence of Spray Drying on Encapsulation Efficiencies and Structure of Casein Micelles Loaded with Anthraquinones Extracted from Aloe vera Plant". Applied Sciences 13, n.º 1 (22 de diciembre de 2022): 110. http://dx.doi.org/10.3390/app13010110.
Texto completoSeitimova, Gulnaz A., Aksholpan K. Shokan, Tatyana G. Tolstikova, Nataliya A. Zhukova, Dmitriy Yu Korulkin, Nataliya O. Kudrina, Yuliya A. Litvinenko, Nataliya D. Meduntseva, Nina V. Terletskaya y Timur E. Kulmanov. "Antiulcer Activity of Anthraquinone–Flavonoid Complex of Rumex tianschanicus Losinsk". Molecules 28, n.º 5 (3 de marzo de 2023): 2347. http://dx.doi.org/10.3390/molecules28052347.
Texto completoKharlamova, T. V. "Anti-fungal activity of anthraquinone derivatives (Part 1)". Chemical Journal of Kazakhstan 78, n.º 2 (15 de junio de 2022): 26–47. http://dx.doi.org/10.51580/2022-2/2710-1185.63.
Texto completoSadiq, Uzma, Harsharn Gill y Jayani Chandrapala. "Ultrasound-Assisted Encapsulation of Anthraquinones Extracted from Aloe-Vera Plant into Casein Micelles". Gels 8, n.º 9 (17 de septiembre de 2022): 597. http://dx.doi.org/10.3390/gels8090597.
Texto completoRoy, Joyeeta, Tanushree Mal, Supriti Jana y Dipakranjan Mal. "Regiodefined synthesis of brominated hydroxyanthraquinones related to proisocrinins". Beilstein Journal of Organic Chemistry 12 (16 de marzo de 2016): 531–36. http://dx.doi.org/10.3762/bjoc.12.52.
Texto completoGupta, Richa K., Ganesh M. S. Thakuri, Gan B. Bajracharya y Ram Narayan Jha. "Synthesis of antioxidative anthraquinones as potential anticancer agents". BIBECHANA 18, n.º 2 (9 de junio de 2021): 143–53. http://dx.doi.org/10.3126/bibechana.v18i2.31234.
Texto completoChakiri, Abdel B. y Philip Hodge. "Synthesis of isopropyl-substituted anthraquinones via Friedel–Crafts acylations: migration of isopropyl groups". Royal Society Open Science 4, n.º 8 (agosto de 2017): 170451. http://dx.doi.org/10.1098/rsos.170451.
Texto completoSu, Guang-Yao, Ming-Long Chen y Kui-Wu Wang. "Natural New Bioactive Anthraquinones from Rubiaceae". Mini-Reviews in Organic Chemistry 17, n.º 7 (9 de octubre de 2020): 872–83. http://dx.doi.org/10.2174/1570193x17666200107092510.
Texto completoShukla, Nivedita, Manmeet Kumar, Akanksha, Ghufran Ahmad, Neha Rahuja, Amar B. Singh, Arvind K. Srivastava, Siron M. Rajendran y Rakesh Maurya. "Tectone, a New Antihyperglycemic Anthraquinone from Tectona grandis Leaves". Natural Product Communications 5, n.º 3 (marzo de 2010): 1934578X1000500. http://dx.doi.org/10.1177/1934578x1000500318.
Texto completoWood, S., J. Huffman, N. Weber, D. Andersen, J. North, B. Murray, R. Sidwell y B. Hughes. "Antiviral Activity of Naturally Occurring Anthraquinones and Anthraquinone Derivatives". Planta Medica 56, n.º 06 (diciembre de 1990): 651–52. http://dx.doi.org/10.1055/s-2006-961304.
Texto completoZhuravleva, Olesya I., Ekaterina A. Chingizova, Galina K. Oleinikova, Sofya S. Starnovskaya, Alexandr S. Antonov, Natalia N. Kirichuk, Alexander S. Menshov et al. "Anthraquinone Derivatives and Other Aromatic Compounds from Marine Fungus Asteromyces cruciatus KMM 4696 and Their Effects against Staphylococcus aureus". Marine Drugs 21, n.º 8 (29 de julio de 2023): 431. http://dx.doi.org/10.3390/md21080431.
Texto completoYuan, Jiaqi, Qian He, Shanshan Song, Xiaofei Zhang, Zehong Miao y Chunhao Yang. "One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones". Molecules 24, n.º 16 (20 de agosto de 2019): 3017. http://dx.doi.org/10.3390/molecules24163017.
Texto completoHa, Nguyen Xuan, Hoang Thi Ngoc Anh, Pham Ngoc Khanh, Vu Thi Ha, Nguyen Viet Ha, Tran Thu Huong y Nguyen Manh Cuong. "In silico and ADMET study of Morinda longissima phytochemicals against TNF‐α for treatment of inflammation‐mediated diseases". Vietnam Journal of Chemistry 61, S1 (julio de 2023): 57–63. http://dx.doi.org/10.1002/vjch.202200214.
Texto completoShupeniuk, Vasyl. "Synthesis and Antimicrobial Activity Of Nitrogen-Containing Anthraquinone Derivatives". Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512) 31, n.º 2 (24 de diciembre de 2022): 193–201. http://dx.doi.org/10.31351/vol31iss2pp193-201.
Texto completoFriedman, Mendel, Alexander Xu, Rani Lee, Daniel N. Nguyen, Tina A. Phan, Sabrina M. Hamada, Rima Panchel et al. "The Inhibitory Activity of Anthraquinones against Pathogenic Protozoa, Bacteria, and Fungi and the Relationship to Structure". Molecules 25, n.º 13 (7 de julio de 2020): 3101. http://dx.doi.org/10.3390/molecules25133101.
Texto completoGlavnik, Vesna y Irena Vovk. "Extraction of Anthraquinones from Japanese Knotweed Rhizomes and Their Analyses by High Performance Thin-Layer Chromatography and Mass Spectrometry". Plants 9, n.º 12 (11 de diciembre de 2020): 1753. http://dx.doi.org/10.3390/plants9121753.
Texto completoCameron, Donald W., Peter G. Griffiths y Andrew G. Riches. "Synthesis of 2,3-Dioxy-1,4-anthraquinones Related to Tetracenomycins C and X". Australian Journal of Chemistry 52, n.º 12 (1999): 1173. http://dx.doi.org/10.1071/ch99181.
Texto completoLi, Xin, Xiao-Ming Li y Bin-Gui Wang. "Structural Revision of Wentiquinone C and Related Congeners from Anthraquinones to Xanthones Using Chemical Derivatization and NMR Analysis". Marine Drugs 17, n.º 1 (24 de diciembre de 2018): 8. http://dx.doi.org/10.3390/md17010008.
Texto completoAndersen, Douglas O., Norbert D. Weber, Steven G. Wood, Bronwyn G. Hughes, Byron K. Murray y James A. North. "In vitro virucidal activity of selected anthraquinones and anthraquinone derivatives". Antiviral Research 16, n.º 2 (septiembre de 1991): 185–96. http://dx.doi.org/10.1016/0166-3542(91)90024-l.
Texto completoShen, Ming-Yi, Yu-Ping Lin, Bei-Chang Yang, Yu-Song Jang, Chih-Kang Chiang, Clément Mettling, Zeng-Weng Chen et al. "Catenarin Prevents Type 1 Diabetes in Nonobese Diabetic Mice via Inhibition of Leukocyte Migration Involving the MEK6/p38 and MEK7/JNK Pathways". Evidence-Based Complementary and Alternative Medicine 2012 (2012): 1–13. http://dx.doi.org/10.1155/2012/982396.
Texto completoARININGSIH, IKA, SOLICHATUN SOLICHATUN y ENDANG ANGGARWULAN. "Callus growth and anthraquinones production of Indian mulberry (Morinda citrifolia L.) in Murashige-Skoog’s medium (MS) supplemented with Ca2+ and Cu2+". Biofarmasi Journal of Natural Product Biochemistry 1, n.º 2 (7 de agosto de 2003): 39–43. http://dx.doi.org/10.13057/biofar/f010201.
Texto completoVONDRÁK, Jan, Jaroslav ŠOUN, Olga VONDRÁKOVແ, Alan M. FRYDAY, Alexander KHODOSOVTSEV y Evgeny A. DAVYDOV. "Absence of anthraquinone pigments is paraphyletic and a phylogenetically unreliable character in the Teloschistaceae". Lichenologist 44, n.º 3 (29 de marzo de 2012): 401–18. http://dx.doi.org/10.1017/s0024282911000843.
Texto completoZhang, Guoying y Xiaofeng Chi. "A green strategy for obtaining anthraquinones from Rheum tanguticum by subcritical water". Open Chemistry 18, n.º 1 (23 de junio de 2020): 702–10. http://dx.doi.org/10.1515/chem-2020-0079.
Texto completoWong, Yee Ching y Haziqah A. Razak. "EXTRACTION OF CRUDE ESSENTIAL FROM SENNA ALATA (POKOK GELENGGANG)". JOURNAL OF ADVANCES IN CHEMISTRY 11, n.º 10 (17 de diciembre de 2016): 3794–806. http://dx.doi.org/10.24297/jac.v11i10.2179.
Texto completoGuin, Partha Sarathi, Piyal Das, Saurabh Das y Parikshit Chandra Mandal. "Interaction of Calf Thymus DNA with the Ni(II) Complex of Sodium 1,4-Dihydroxy-9,10-Anthraquinone-2-Sulphonate: A Novel Method of Analysis Using Cyclic Voltammetry". International Journal of Electrochemistry 2012 (2012): 1–10. http://dx.doi.org/10.1155/2012/183745.
Texto completoYang, Wen-Chin, Ming-Yi Shen, Yu-Song Jang, Zeng-Weng Chen y Cicero Chang. "Catenarin, an anthraquinone compound, inhibits CXCR4 and CCR5 pathways to protect against type 1 diabetes in NOD mice (72.1)". Journal of Immunology 188, n.º 1_Supplement (1 de mayo de 2012): 72.1. http://dx.doi.org/10.4049/jimmunol.188.supp.72.1.
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