Artykuły w czasopismach na temat „Anthraquinone”
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Drummond, Christopher A., Maria Teresa Molina, Sandra Taliansky, Carl R. Breidenbach i 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.
Pełny tekst źródłaMalak, Lourin G., Daoud W. Bishay, Afaf M. Abdel-Baky, Ahmed M. Moharram, Stephen J. Cutler i Samir A. Ross. "New Anthraquinone Derivatives from Geosmithia lavendula". Natural Product Communications 8, nr 2 (luty 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800215.
Pełny tekst źródłaGao, Huiyu, Jianbo Yang, Xueting Wang, Yunfei Song, Xianlong Cheng, Feng Wei, Ying Wang, Donglin Gu, Hua Sun i Shuangcheng Ma. "Exploratory Quality Control Study for Polygonum multiflorum Thunb. Using Dinuclear Anthraquinones with Potential Hepatotoxicity". Molecules 27, nr 19 (10.10.2022): 6760. http://dx.doi.org/10.3390/molecules27196760.
Pełny tekst źródłaBranco, Alexsandro, Angelo C. Pinto, Jan Schripsema i Raimundo Braz-Filho. "Anthraquinones from the bark of Senna macranthera". Anais da Academia Brasileira de Ciências 83, nr 4 (grudzień 2011): 1159–64. http://dx.doi.org/10.1590/s0001-37652011000400003.
Pełny tekst źródłaZhang, Rongfei, Yuanyuan Miao, Lingyun Chen, Shanyong Yi i Ninghua Tan. "De Novo Transcriptome Analysis Reveals Putative Genes Involved in Anthraquinone Biosynthesis in Rubia yunnanensis". Genes 13, nr 3 (16.03.2022): 521. http://dx.doi.org/10.3390/genes13030521.
Pełny tekst źródłaUllah, Hossain, Junhyeong Kim, Naveed Rehman, Hye-Jin Kim, Mi-Jeong Ahn i 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, nr 3 (20.07.2018): 100. http://dx.doi.org/10.3390/pharmaceutics10030100.
Pełny tekst źródłaYang, Yong, Qiao-Xia Wu i Min Xue. "Bifurcated hydrogen bonding mediated planar 9,10-anthraquinone dyes: synthesis, structure and properties". RSC Advances 5, nr 37 (2015): 28932–37. http://dx.doi.org/10.1039/c5ra01682g.
Pełny tekst źródłaManojlovic, N. T., S. Solujic, S. Sukdolak i Lj Krstic. "Isolation and antimicrobial activity of anthraquinones from some species of the lichen genus Xanthoria". Journal of the Serbian Chemical Society 65, nr 8 (2000): 555–60. http://dx.doi.org/10.2298/jsc0008555m.
Pełny tekst źródłaAmmar Rushdan, Nur Afiqah Nadhiah, Nurunajah Ab Ghani i Nurulfazlina Edayah Rasol. "Review on Anthraquinones Isolated from Rubiaceae Family". Journal of Science and Mathematics Letters 11, Special (9.11.2023): 163–74. http://dx.doi.org/10.37134/jsml.vol11.sp.18.2023.
Pełny tekst źródłaHafez Ghoran, Salar, Fatemeh Taktaz, Seyed Abdulmajid Ayatollahi i Anake Kijjoa. "Anthraquinones and Their Analogues from Marine-Derived Fungi: Chemistry and Biological Activities". Marine Drugs 20, nr 8 (25.07.2022): 474. http://dx.doi.org/10.3390/md20080474.
Pełny tekst źródłaGriffiths, Scott, Carl H. Mesarich, Benedetta Saccomanno, Abraham Vaisberg, Pierre J. G. M. De Wit, Russell Cox i Jérôme Collemare. "Elucidation of cladofulvin biosynthesis reveals a cytochrome P450 monooxygenase required for anthraquinone dimerization". Proceedings of the National Academy of Sciences 113, nr 25 (6.06.2016): 6851–56. http://dx.doi.org/10.1073/pnas.1603528113.
Pełny tekst źródłaHynninen, Paavo H., Riikka Räisänen, Pia Elovaara i Eila Nokelainen. "Preparative Isolation of Anthraquinones from the Fungus Dermocybe sanguined Using Enzymatic Hydrolysis by the Endogenous β-Glucosidase". Zeitschrift für Naturforschung C 55, nr 7-8 (1.08.2000): 600–610. http://dx.doi.org/10.1515/znc-2000-7-820.
Pełny tekst źródłaAnderson, Benjamin R., i Mark G. Kuzyk. "Imaging studies of photodegradation and self-healing in anthraquinone derivative dye-doped PMMA". Physical Chemistry Chemical Physics 22, nr 48 (2020): 28154–64. http://dx.doi.org/10.1039/d0cp05426g.
Pełny tekst źródłaPark, Jae Gwang, Seung Cheol Kim, Yun Hwan Kim, Woo Seok Yang, Yong Kim, Sungyoul Hong, Kyung-Hee Kim i in. "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.
Pełny tekst źródłaSadiq, Uzma, Fatima Shahid, Harsharn Gill i Jayani Chandrapala. "The Release Behavior of Anthraquinones Encapsulated into Casein Micelles during In Vitro Digestion". Foods 12, nr 15 (27.07.2023): 2844. http://dx.doi.org/10.3390/foods12152844.
Pełny tekst źródłaLyčka, Antonín, Libuše Havlíčková, Alois Koloničný i 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, nr 3 (1987): 736–41. http://dx.doi.org/10.1135/cccc19870736.
Pełny tekst źródłaBoniface, PJ, RC Cambie, C. Higgs, PS Rutledge i 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, nr 6 (1995): 1089. http://dx.doi.org/10.1071/ch9951089.
Pełny tekst źródłaLaub, Annegret, Ann-Katrin Sendatzki, Götz Palfner, Ludger A. Wessjohann, Jürgen Schmidt i 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, nr 2 (6.02.2020): 156. http://dx.doi.org/10.3390/foods9020156.
Pełny tekst źródłaBussmann, Rainer W., Lothar Hennig, Athanassios Giannis, Jutta Ortwein, Toni M. Kutchan i 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.
Pełny tekst źródłaLi, Rong-Rong, Xue-Fang Liu, Su-Xiang Feng, Sheng-Nan Shu, Pei-Yang Wang, Na Zhang, Jian-Sheng Li i 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, nr 10 (17.05.2019): 1898. http://dx.doi.org/10.3390/molecules24101898.
Pełny tekst źródłaOsman, Che Puteh, i Nor Hadiani Ismail. "A REVIEW ON THE CHEMISTRY AND PHARMACOLOGY OF Rennellia elliptica Korth". Indonesian Journal of Tropical and Infectious Disease 6, nr 6 (21.12.2017): 131. http://dx.doi.org/10.20473/ijtid.v6i6.6642.
Pełny tekst źródłaChee, Cheok Wui, Nor Hisam Zamakshshari, Vannajan Sanghiran Lee, Iskandar Abdullah, Rozana Othman, Yean Kee Lee, Najihah Mohd Hashim i Nurshamimi Nor Rashid. "Morindone from Morinda citrifolia as a potential antiproliferative agent against colorectal cancer cell lines". PLOS ONE 17, nr 7 (12.07.2022): e0270970. http://dx.doi.org/10.1371/journal.pone.0270970.
Pełny tekst źródłaHung, Hsin-Yi, Kun-Ching Cheng, Ping-Chung Kuo, I.-Tsen Chen, Yue-Chiun Li, Tsong-Long Hwang, Sio-Hong Lam i Tian-Shung Wu. "Chemical Constituents of Hedyotis diffusa and Their Anti-Inflammatory Bioactivities". Antioxidants 11, nr 2 (9.02.2022): 335. http://dx.doi.org/10.3390/antiox11020335.
Pełny tekst źródłaKunze, Arno, Ludger Witte, Manuel Aregullin, Eloy Rodriguez i Peter Proksch. "Anthraquinones in the Leaf Beetle Trirhabda geminata (Chrysomelidae)". Zeitschrift für Naturforschung C 51, nr 3-4 (1.04.1996): 249–52. http://dx.doi.org/10.1515/znc-1996-3-417.
Pełny tekst źródłaSadiq, Uzma, Harsharn Gill, Jayani Chandrapala i 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, nr 1 (22.12.2022): 110. http://dx.doi.org/10.3390/app13010110.
Pełny tekst źródłaSeitimova, 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 i Timur E. Kulmanov. "Antiulcer Activity of Anthraquinone–Flavonoid Complex of Rumex tianschanicus Losinsk". Molecules 28, nr 5 (3.03.2023): 2347. http://dx.doi.org/10.3390/molecules28052347.
Pełny tekst źródłaKharlamova, T. V. "Anti-fungal activity of anthraquinone derivatives (Part 1)". Chemical Journal of Kazakhstan 78, nr 2 (15.06.2022): 26–47. http://dx.doi.org/10.51580/2022-2/2710-1185.63.
Pełny tekst źródłaSadiq, Uzma, Harsharn Gill i Jayani Chandrapala. "Ultrasound-Assisted Encapsulation of Anthraquinones Extracted from Aloe-Vera Plant into Casein Micelles". Gels 8, nr 9 (17.09.2022): 597. http://dx.doi.org/10.3390/gels8090597.
Pełny tekst źródłaRoy, Joyeeta, Tanushree Mal, Supriti Jana i Dipakranjan Mal. "Regiodefined synthesis of brominated hydroxyanthraquinones related to proisocrinins". Beilstein Journal of Organic Chemistry 12 (16.03.2016): 531–36. http://dx.doi.org/10.3762/bjoc.12.52.
Pełny tekst źródłaGupta, Richa K., Ganesh M. S. Thakuri, Gan B. Bajracharya i Ram Narayan Jha. "Synthesis of antioxidative anthraquinones as potential anticancer agents". BIBECHANA 18, nr 2 (9.06.2021): 143–53. http://dx.doi.org/10.3126/bibechana.v18i2.31234.
Pełny tekst źródłaChakiri, Abdel B., i Philip Hodge. "Synthesis of isopropyl-substituted anthraquinones via Friedel–Crafts acylations: migration of isopropyl groups". Royal Society Open Science 4, nr 8 (sierpień 2017): 170451. http://dx.doi.org/10.1098/rsos.170451.
Pełny tekst źródłaSu, Guang-Yao, Ming-Long Chen i Kui-Wu Wang. "Natural New Bioactive Anthraquinones from Rubiaceae". Mini-Reviews in Organic Chemistry 17, nr 7 (9.10.2020): 872–83. http://dx.doi.org/10.2174/1570193x17666200107092510.
Pełny tekst źródłaShukla, Nivedita, Manmeet Kumar, Akanksha, Ghufran Ahmad, Neha Rahuja, Amar B. Singh, Arvind K. Srivastava, Siron M. Rajendran i Rakesh Maurya. "Tectone, a New Antihyperglycemic Anthraquinone from Tectona grandis Leaves". Natural Product Communications 5, nr 3 (marzec 2010): 1934578X1000500. http://dx.doi.org/10.1177/1934578x1000500318.
Pełny tekst źródłaWood, S., J. Huffman, N. Weber, D. Andersen, J. North, B. Murray, R. Sidwell i B. Hughes. "Antiviral Activity of Naturally Occurring Anthraquinones and Anthraquinone Derivatives". Planta Medica 56, nr 06 (grudzień 1990): 651–52. http://dx.doi.org/10.1055/s-2006-961304.
Pełny tekst źródłaZhuravleva, Olesya I., Ekaterina A. Chingizova, Galina K. Oleinikova, Sofya S. Starnovskaya, Alexandr S. Antonov, Natalia N. Kirichuk, Alexander S. Menshov i in. "Anthraquinone Derivatives and Other Aromatic Compounds from Marine Fungus Asteromyces cruciatus KMM 4696 and Their Effects against Staphylococcus aureus". Marine Drugs 21, nr 8 (29.07.2023): 431. http://dx.doi.org/10.3390/md21080431.
Pełny tekst źródłaYuan, Jiaqi, Qian He, Shanshan Song, Xiaofei Zhang, Zehong Miao i Chunhao Yang. "One Pot and Metal-Free Approach to 3-(2-Hydroxybenzoyl)-1-aza-anthraquinones". Molecules 24, nr 16 (20.08.2019): 3017. http://dx.doi.org/10.3390/molecules24163017.
Pełny tekst źródłaHa, Nguyen Xuan, Hoang Thi Ngoc Anh, Pham Ngoc Khanh, Vu Thi Ha, Nguyen Viet Ha, Tran Thu Huong i 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 (lipiec 2023): 57–63. http://dx.doi.org/10.1002/vjch.202200214.
Pełny tekst źródłaShupeniuk, Vasyl. "Synthesis and Antimicrobial Activity Of Nitrogen-Containing Anthraquinone Derivatives". Iraqi Journal of Pharmaceutical Sciences ( P-ISSN 1683 - 3597 E-ISSN 2521 - 3512) 31, nr 2 (24.12.2022): 193–201. http://dx.doi.org/10.31351/vol31iss2pp193-201.
Pełny tekst źródłaFriedman, Mendel, Alexander Xu, Rani Lee, Daniel N. Nguyen, Tina A. Phan, Sabrina M. Hamada, Rima Panchel i in. "The Inhibitory Activity of Anthraquinones against Pathogenic Protozoa, Bacteria, and Fungi and the Relationship to Structure". Molecules 25, nr 13 (7.07.2020): 3101. http://dx.doi.org/10.3390/molecules25133101.
Pełny tekst źródłaGlavnik, Vesna, i Irena Vovk. "Extraction of Anthraquinones from Japanese Knotweed Rhizomes and Their Analyses by High Performance Thin-Layer Chromatography and Mass Spectrometry". Plants 9, nr 12 (11.12.2020): 1753. http://dx.doi.org/10.3390/plants9121753.
Pełny tekst źródłaCameron, Donald W., Peter G. Griffiths i Andrew G. Riches. "Synthesis of 2,3-Dioxy-1,4-anthraquinones Related to Tetracenomycins C and X". Australian Journal of Chemistry 52, nr 12 (1999): 1173. http://dx.doi.org/10.1071/ch99181.
Pełny tekst źródłaLi, Xin, Xiao-Ming Li i Bin-Gui Wang. "Structural Revision of Wentiquinone C and Related Congeners from Anthraquinones to Xanthones Using Chemical Derivatization and NMR Analysis". Marine Drugs 17, nr 1 (24.12.2018): 8. http://dx.doi.org/10.3390/md17010008.
Pełny tekst źródłaAndersen, Douglas O., Norbert D. Weber, Steven G. Wood, Bronwyn G. Hughes, Byron K. Murray i James A. North. "In vitro virucidal activity of selected anthraquinones and anthraquinone derivatives". Antiviral Research 16, nr 2 (wrzesień 1991): 185–96. http://dx.doi.org/10.1016/0166-3542(91)90024-l.
Pełny tekst źródłaShen, Ming-Yi, Yu-Ping Lin, Bei-Chang Yang, Yu-Song Jang, Chih-Kang Chiang, Clément Mettling, Zeng-Weng Chen i in. "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.
Pełny tekst źródłaARININGSIH, IKA, SOLICHATUN SOLICHATUN i 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, nr 2 (7.08.2003): 39–43. http://dx.doi.org/10.13057/biofar/f010201.
Pełny tekst źródłaVONDRÁK, Jan, Jaroslav ŠOUN, Olga VONDRÁKOVແ, Alan M. FRYDAY, Alexander KHODOSOVTSEV i Evgeny A. DAVYDOV. "Absence of anthraquinone pigments is paraphyletic and a phylogenetically unreliable character in the Teloschistaceae". Lichenologist 44, nr 3 (29.03.2012): 401–18. http://dx.doi.org/10.1017/s0024282911000843.
Pełny tekst źródłaZhang, Guoying, i Xiaofeng Chi. "A green strategy for obtaining anthraquinones from Rheum tanguticum by subcritical water". Open Chemistry 18, nr 1 (23.06.2020): 702–10. http://dx.doi.org/10.1515/chem-2020-0079.
Pełny tekst źródłaWong, Yee Ching, i Haziqah A. Razak. "EXTRACTION OF CRUDE ESSENTIAL FROM SENNA ALATA (POKOK GELENGGANG)". JOURNAL OF ADVANCES IN CHEMISTRY 11, nr 10 (17.12.2016): 3794–806. http://dx.doi.org/10.24297/jac.v11i10.2179.
Pełny tekst źródłaGuin, Partha Sarathi, Piyal Das, Saurabh Das i 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.
Pełny tekst źródłaYang, Wen-Chin, Ming-Yi Shen, Yu-Song Jang, Zeng-Weng Chen i 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, nr 1_Supplement (1.05.2012): 72.1. http://dx.doi.org/10.4049/jimmunol.188.supp.72.1.
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