Статті в журналах з теми "Anthraquinone"
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Drummond, Christopher A., Maria Teresa Molina, Sandra Taliansky, Carl R. Breidenbach, and 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.
Повний текст джерелаMalak, Lourin G., Daoud W. Bishay, Afaf M. Abdel-Baky, Ahmed M. Moharram, Stephen J. Cutler, and Samir A. Ross. "New Anthraquinone Derivatives from Geosmithia lavendula." Natural Product Communications 8, no. 2 (February 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800215.
Повний текст джерелаGao, Huiyu, Jianbo Yang, Xueting Wang, Yunfei Song, Xianlong Cheng, Feng Wei, Ying Wang, Donglin Gu, Hua Sun, and Shuangcheng Ma. "Exploratory Quality Control Study for Polygonum multiflorum Thunb. Using Dinuclear Anthraquinones with Potential Hepatotoxicity." Molecules 27, no. 19 (October 10, 2022): 6760. http://dx.doi.org/10.3390/molecules27196760.
Повний текст джерелаBranco, Alexsandro, Angelo C. Pinto, Jan Schripsema, and Raimundo Braz-Filho. "Anthraquinones from the bark of Senna macranthera." Anais da Academia Brasileira de Ciências 83, no. 4 (December 2011): 1159–64. http://dx.doi.org/10.1590/s0001-37652011000400003.
Повний текст джерелаZhang, Rongfei, Yuanyuan Miao, Lingyun Chen, Shanyong Yi, and Ninghua Tan. "De Novo Transcriptome Analysis Reveals Putative Genes Involved in Anthraquinone Biosynthesis in Rubia yunnanensis." Genes 13, no. 3 (March 16, 2022): 521. http://dx.doi.org/10.3390/genes13030521.
Повний текст джерелаUllah, Hossain, Junhyeong Kim, Naveed Rehman, Hye-Jin Kim, Mi-Jeong Ahn, and 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, no. 3 (July 20, 2018): 100. http://dx.doi.org/10.3390/pharmaceutics10030100.
Повний текст джерелаYang, Yong, Qiao-Xia Wu, and Min Xue. "Bifurcated hydrogen bonding mediated planar 9,10-anthraquinone dyes: synthesis, structure and properties." RSC Advances 5, no. 37 (2015): 28932–37. http://dx.doi.org/10.1039/c5ra01682g.
Повний текст джерелаManojlovic, N. T., S. Solujic, S. Sukdolak, and Lj Krstic. "Isolation and antimicrobial activity of anthraquinones from some species of the lichen genus Xanthoria." Journal of the Serbian Chemical Society 65, no. 8 (2000): 555–60. http://dx.doi.org/10.2298/jsc0008555m.
Повний текст джерелаAmmar Rushdan, Nur Afiqah Nadhiah, Nurunajah Ab Ghani, and Nurulfazlina Edayah Rasol. "Review on Anthraquinones Isolated from Rubiaceae Family." Journal of Science and Mathematics Letters 11, Special (November 9, 2023): 163–74. http://dx.doi.org/10.37134/jsml.vol11.sp.18.2023.
Повний текст джерелаHafez Ghoran, Salar, Fatemeh Taktaz, Seyed Abdulmajid Ayatollahi, and Anake Kijjoa. "Anthraquinones and Their Analogues from Marine-Derived Fungi: Chemistry and Biological Activities." Marine Drugs 20, no. 8 (July 25, 2022): 474. http://dx.doi.org/10.3390/md20080474.
Повний текст джерелаGriffiths, Scott, Carl H. Mesarich, Benedetta Saccomanno, Abraham Vaisberg, Pierre J. G. M. De Wit, Russell Cox, and Jérôme Collemare. "Elucidation of cladofulvin biosynthesis reveals a cytochrome P450 monooxygenase required for anthraquinone dimerization." Proceedings of the National Academy of Sciences 113, no. 25 (June 6, 2016): 6851–56. http://dx.doi.org/10.1073/pnas.1603528113.
Повний текст джерелаHynninen, Paavo H., Riikka Räisänen, Pia Elovaara та Eila Nokelainen. "Preparative Isolation of Anthraquinones from the Fungus Dermocybe sanguined Using Enzymatic Hydrolysis by the Endogenous β-Glucosidase". Zeitschrift für Naturforschung C 55, № 7-8 (1 серпня 2000): 600–610. http://dx.doi.org/10.1515/znc-2000-7-820.
Повний текст джерелаAnderson, Benjamin R., and Mark G. Kuzyk. "Imaging studies of photodegradation and self-healing in anthraquinone derivative dye-doped PMMA." Physical Chemistry Chemical Physics 22, no. 48 (2020): 28154–64. http://dx.doi.org/10.1039/d0cp05426g.
Повний текст джерелаPark, 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.
Повний текст джерелаSadiq, Uzma, Fatima Shahid, Harsharn Gill, and Jayani Chandrapala. "The Release Behavior of Anthraquinones Encapsulated into Casein Micelles during In Vitro Digestion." Foods 12, no. 15 (July 27, 2023): 2844. http://dx.doi.org/10.3390/foods12152844.
Повний текст джерелаLyčka, Antonín, Libuše Havlíčková, Alois Koloničný, and 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, no. 3 (1987): 736–41. http://dx.doi.org/10.1135/cccc19870736.
Повний текст джерелаBoniface, PJ, RC Cambie, C. Higgs, PS Rutledge, and 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, no. 6 (1995): 1089. http://dx.doi.org/10.1071/ch9951089.
Повний текст джерелаLaub, Annegret, Ann-Katrin Sendatzki, Götz Palfner, Ludger A. Wessjohann, Jürgen Schmidt, and 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, no. 2 (February 6, 2020): 156. http://dx.doi.org/10.3390/foods9020156.
Повний текст джерелаBussmann, Rainer W., Lothar Hennig, Athanassios Giannis, Jutta Ortwein, Toni M. Kutchan, and 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.
Повний текст джерелаLi, Rong-Rong, Xue-Fang Liu, Su-Xiang Feng, Sheng-Nan Shu, Pei-Yang Wang, Na Zhang, Jian-Sheng Li, and 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, no. 10 (May 17, 2019): 1898. http://dx.doi.org/10.3390/molecules24101898.
Повний текст джерелаOsman, Che Puteh, and Nor Hadiani Ismail. "A REVIEW ON THE CHEMISTRY AND PHARMACOLOGY OF Rennellia elliptica Korth." Indonesian Journal of Tropical and Infectious Disease 6, no. 6 (December 21, 2017): 131. http://dx.doi.org/10.20473/ijtid.v6i6.6642.
Повний текст джерелаChee, Cheok Wui, Nor Hisam Zamakshshari, Vannajan Sanghiran Lee, Iskandar Abdullah, Rozana Othman, Yean Kee Lee, Najihah Mohd Hashim, and Nurshamimi Nor Rashid. "Morindone from Morinda citrifolia as a potential antiproliferative agent against colorectal cancer cell lines." PLOS ONE 17, no. 7 (July 12, 2022): e0270970. http://dx.doi.org/10.1371/journal.pone.0270970.
Повний текст джерелаHung, Hsin-Yi, Kun-Ching Cheng, Ping-Chung Kuo, I.-Tsen Chen, Yue-Chiun Li, Tsong-Long Hwang, Sio-Hong Lam, and Tian-Shung Wu. "Chemical Constituents of Hedyotis diffusa and Their Anti-Inflammatory Bioactivities." Antioxidants 11, no. 2 (February 9, 2022): 335. http://dx.doi.org/10.3390/antiox11020335.
Повний текст джерелаKunze, Arno, Ludger Witte, Manuel Aregullin, Eloy Rodriguez, and Peter Proksch. "Anthraquinones in the Leaf Beetle Trirhabda geminata (Chrysomelidae)." Zeitschrift für Naturforschung C 51, no. 3-4 (April 1, 1996): 249–52. http://dx.doi.org/10.1515/znc-1996-3-417.
Повний текст джерелаSadiq, Uzma, Harsharn Gill, Jayani Chandrapala, and 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, no. 1 (December 22, 2022): 110. http://dx.doi.org/10.3390/app13010110.
Повний текст джерелаSeitimova, 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, and Timur E. Kulmanov. "Antiulcer Activity of Anthraquinone–Flavonoid Complex of Rumex tianschanicus Losinsk." Molecules 28, no. 5 (March 3, 2023): 2347. http://dx.doi.org/10.3390/molecules28052347.
Повний текст джерелаKharlamova, T. V. "Anti-fungal activity of anthraquinone derivatives (Part 1)." Chemical Journal of Kazakhstan 78, no. 2 (June 15, 2022): 26–47. http://dx.doi.org/10.51580/2022-2/2710-1185.63.
Повний текст джерелаSadiq, Uzma, Harsharn Gill, and Jayani Chandrapala. "Ultrasound-Assisted Encapsulation of Anthraquinones Extracted from Aloe-Vera Plant into Casein Micelles." Gels 8, no. 9 (September 17, 2022): 597. http://dx.doi.org/10.3390/gels8090597.
Повний текст джерелаRoy, Joyeeta, Tanushree Mal, Supriti Jana, and Dipakranjan Mal. "Regiodefined synthesis of brominated hydroxyanthraquinones related to proisocrinins." Beilstein Journal of Organic Chemistry 12 (March 16, 2016): 531–36. http://dx.doi.org/10.3762/bjoc.12.52.
Повний текст джерелаGupta, Richa K., Ganesh M. S. Thakuri, Gan B. Bajracharya, and Ram Narayan Jha. "Synthesis of antioxidative anthraquinones as potential anticancer agents." BIBECHANA 18, no. 2 (June 9, 2021): 143–53. http://dx.doi.org/10.3126/bibechana.v18i2.31234.
Повний текст джерелаChakiri, Abdel B., and Philip Hodge. "Synthesis of isopropyl-substituted anthraquinones via Friedel–Crafts acylations: migration of isopropyl groups." Royal Society Open Science 4, no. 8 (August 2017): 170451. http://dx.doi.org/10.1098/rsos.170451.
Повний текст джерелаSu, Guang-Yao, Ming-Long Chen, and Kui-Wu Wang. "Natural New Bioactive Anthraquinones from Rubiaceae." Mini-Reviews in Organic Chemistry 17, no. 7 (October 9, 2020): 872–83. http://dx.doi.org/10.2174/1570193x17666200107092510.
Повний текст джерелаShukla, Nivedita, Manmeet Kumar, Akanksha, Ghufran Ahmad, Neha Rahuja, Amar B. Singh, Arvind K. Srivastava, Siron M. Rajendran, and Rakesh Maurya. "Tectone, a New Antihyperglycemic Anthraquinone from Tectona grandis Leaves." Natural Product Communications 5, no. 3 (March 2010): 1934578X1000500. http://dx.doi.org/10.1177/1934578x1000500318.
Повний текст джерелаWood, S., J. Huffman, N. Weber, D. Andersen, J. North, B. Murray, R. Sidwell, and B. Hughes. "Antiviral Activity of Naturally Occurring Anthraquinones and Anthraquinone Derivatives." Planta Medica 56, no. 06 (December 1990): 651–52. http://dx.doi.org/10.1055/s-2006-961304.
Повний текст джерелаZhuravleva, 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, no. 8 (July 29, 2023): 431. http://dx.doi.org/10.3390/md21080431.
Повний текст джерелаYuan, Jiaqi, Qian He, Shanshan Song, Xiaofei Zhang, Zehong Miao, and Chunhao Yang. "One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones." Molecules 24, no. 16 (August 20, 2019): 3017. http://dx.doi.org/10.3390/molecules24163017.
Повний текст джерелаHa, Nguyen Xuan, Hoang Thi Ngoc Anh, Pham Ngoc Khanh, Vu Thi Ha, Nguyen Viet Ha, Tran Thu Huong та 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 (липень 2023): 57–63. http://dx.doi.org/10.1002/vjch.202200214.
Повний текст джерелаShupeniuk, Vasyl. "Synthesis and Antimicrobial Activity Of Nitrogen-Containing Anthraquinone Derivatives." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512) 31, no. 2 (December 24, 2022): 193–201. http://dx.doi.org/10.31351/vol31iss2pp193-201.
Повний текст джерелаFriedman, 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, no. 13 (July 7, 2020): 3101. http://dx.doi.org/10.3390/molecules25133101.
Повний текст джерелаGlavnik, Vesna, and Irena Vovk. "Extraction of Anthraquinones from Japanese Knotweed Rhizomes and Their Analyses by High Performance Thin-Layer Chromatography and Mass Spectrometry." Plants 9, no. 12 (December 11, 2020): 1753. http://dx.doi.org/10.3390/plants9121753.
Повний текст джерелаCameron, Donald W., Peter G. Griffiths, and Andrew G. Riches. "Synthesis of 2,3-Dioxy-1,4-anthraquinones Related to Tetracenomycins C and X." Australian Journal of Chemistry 52, no. 12 (1999): 1173. http://dx.doi.org/10.1071/ch99181.
Повний текст джерелаLi, Xin, Xiao-Ming Li, and Bin-Gui Wang. "Structural Revision of Wentiquinone C and Related Congeners from Anthraquinones to Xanthones Using Chemical Derivatization and NMR Analysis." Marine Drugs 17, no. 1 (December 24, 2018): 8. http://dx.doi.org/10.3390/md17010008.
Повний текст джерелаAndersen, Douglas O., Norbert D. Weber, Steven G. Wood, Bronwyn G. Hughes, Byron K. Murray, and James A. North. "In vitro virucidal activity of selected anthraquinones and anthraquinone derivatives." Antiviral Research 16, no. 2 (September 1991): 185–96. http://dx.doi.org/10.1016/0166-3542(91)90024-l.
Повний текст джерелаShen, 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.
Повний текст джерелаARININGSIH, IKA, SOLICHATUN SOLICHATUN, and 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, no. 2 (August 7, 2003): 39–43. http://dx.doi.org/10.13057/biofar/f010201.
Повний текст джерелаVONDRÁK, Jan, Jaroslav ŠOUN, Olga VONDRÁKOVແ, Alan M. FRYDAY, Alexander KHODOSOVTSEV, and Evgeny A. DAVYDOV. "Absence of anthraquinone pigments is paraphyletic and a phylogenetically unreliable character in the Teloschistaceae." Lichenologist 44, no. 3 (March 29, 2012): 401–18. http://dx.doi.org/10.1017/s0024282911000843.
Повний текст джерелаZhang, Guoying, and Xiaofeng Chi. "A green strategy for obtaining anthraquinones from Rheum tanguticum by subcritical water." Open Chemistry 18, no. 1 (June 23, 2020): 702–10. http://dx.doi.org/10.1515/chem-2020-0079.
Повний текст джерелаWong, Yee Ching, and Haziqah A. Razak. "EXTRACTION OF CRUDE ESSENTIAL FROM SENNA ALATA (POKOK GELENGGANG)." JOURNAL OF ADVANCES IN CHEMISTRY 11, no. 10 (December 17, 2016): 3794–806. http://dx.doi.org/10.24297/jac.v11i10.2179.
Повний текст джерелаGuin, Partha Sarathi, Piyal Das, Saurabh Das, and 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.
Повний текст джерелаYang, Wen-Chin, Ming-Yi Shen, Yu-Song Jang, Zeng-Weng Chen, and 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, no. 1_Supplement (May 1, 2012): 72.1. http://dx.doi.org/10.4049/jimmunol.188.supp.72.1.
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