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Qian Zhou, Huitian Du, Zhen Chen, Yuan Yu, Junfeng Ren, Shenghao Han, Jihui Fan & Zhiyong Pang. (2022) Two-photon excited fluorescence from ground-state charge-transfer cocrystals of acridine and 1,2,4,5-tetracyano-benzene. Dyes and Pigments 198, pages 109965.
Crossref
Crossref
Igor O. Fritsky, Valerii Y. Sirenko, Sergiu Shova, Olesia I. Kucheriv & Il'ya A. Gural'skiy. (2021)
Crystal structure of 9-aminoacridinium chloride
N
,
N
-dimethylformamide monosolvate
. Acta Crystallographica Section E Crystallographic Communications 77:12, pages 1303-1306.
Crossref
Crossref
Kamila Rząd, Ewa Paluszkiewicz & Iwona Gabriel. (2021) A new 1-nitro-9-aminoacridine derivative targeting yeast topoisomerase II able to overcome fluconazole-resistance. Bioorganic & Medicinal Chemistry Letters 35, pages 127815.
Crossref
Crossref
Antonios Georgakopoulos, Amalia D. Kalampaliki, Katerina Gioti, Sami Hamdoun, Aikaterini F. Giannopoulou, Thomas Efferth, Dimitrios J. Stravopodis, Roxane Tenta, Panagiotis Marakos, Nicole Pouli & Ioannis K. Kostakis. (2020) Synthesis of novel xanthone and acridone carboxamides with potent antiproliferative activities. Arabian Journal of Chemistry 13:11, pages 7953-7969.
Crossref
Crossref
Maria Karelou, Vasileios Kourafalos, Athanasia P. Tragomalou, Panagiotis Marakos, Nicole Pouli, Ourania E. Tsitsilonis, Evangelos Gikas & Ioannis K. Kostakis. (2020) Synthesis, Biological Evaluation and Stability Studies of Some Novel Aza-Acridine Aminoderivatives. Molecules 25:19, pages 4584.
Crossref
Crossref
Weixin Ma, Luoqiang Zhang, Yang Shi, You Ran, Yang Liu & Jingsong You. (2020) Molecular Engineering to Access Fluorescent Trackers of Organelles by Cyclization: Chemical Environment of Nitrogen Atom‐Modulated Targets. Advanced Functional Materials 30:42, pages 2004511.
Crossref
Crossref
Assem Barakat, Saied M. Soliman, Ayman El-Faham, M. Ali, Abdullah Mohammed Al-Majid, Sammer Yousuf & M. Iqbal Choudhary. (2019) Three Multi-Components Reaction: Synthesis and X-Ray Single-Crystal of Hydroacridinone-Based Hydrazino-S-Triazine Derivative as a New Class of Urease Inhibitor. Crystals 10:1, pages 14.
Crossref
Crossref
Jiao Liu, Hao Fang, Rui Cheng, Zhishuo Wang, Yudong Yang & Jingsong You. (2019)
Cascade intramolecular imidoylation and C–H activation/annulation of benzimidoyl chlorides with alkynes: one-pot synthesis of 7
H
-dibenzo[
de
,
h
]quinoline analogues
. Chemical Communications 55:49, pages 7097-7100.
Crossref
Crossref
Olla Sharhan, Thorsten Heidelberg, Najiahah Mohd HashimAbbas Abdulameer Salman, Hapipah Mohd Ali & Soher Nagi Jayash. (2018) Synthesis and biological study of acridine-based imidazolium salts. RSC Advances 8:68, pages 38995-39004.
Crossref
Crossref
Ning Wang, Bin Zhang, Feng Jin, Dan Gao, Feng Liu, Hongxia Liu & Yuyang Jiang. (2018) Combing metabolomics with bioanalysis methods to study the antitumor mechanism of the new acridone derivative 8q on CCRF-CEM cells: 8q induced mitochondrial-mediated apoptosis and targeted the PI3K/AKT/FOXO1 pathway. Journal of Pharmaceutical and Biomedical Analysis 160, pages 314-322.
Crossref
Crossref
Katarzyna Nowak. (2017) Chemical structures and biological activities of bis- and tetrakis-acridine derivatives: A review. Journal of Molecular Structure 1146, pages 562-570.
Crossref
Crossref
Fang-Ming Wang, Dan Bao, Bing-Xiang Hu, Ze-Yu Zhou, Deng-Deng Huang, Li-Zhuang Chen & Yuan-Yuan Dan. (2017)
Synthesis of 10-substituted 3,6-Diphenyl-9-aryl-3,4,6,7,9,10-hexahydro-acridine-1,8(2
H
,5
H
)-dione Derivatives and Biological Activities
. Journal of Heterocyclic Chemistry 54:1, pages 784-788.
Crossref
Crossref
Wei Zhang, Bin Zhang, Wei Zhang, Ti Yang, Ning Wang, Chunmei Gao, Chunyan Tan, Hongxia Liu & Yuyang Jiang. (2016) Synthesis and antiproliferative activity of 9-benzylamino-6-chloro-2-methoxy-acridine derivatives as potent DNA-binding ligands and topoisomerase II inhibitors. European Journal of Medicinal Chemistry 116, pages 59-70.
Crossref
Crossref
İbrahim Esirden, Ramazan Ulus, Burak Aday, Muhammet Tanç, Claudiu T. Supuran & Muharrem Kaya. (2015) Synthesis of novel acridine bis-sulfonamides with effective inhibitory activity against the carbonic anhydrase isoforms I, II, IX and XII. Bioorganic & Medicinal Chemistry 23:20, pages 6573-6580.
Crossref
Crossref
Fang-Ming Wang, Dan Bao, Bing-Xiang Hu, Ze-Yu Zhou, Deng-Deng Huang, Li-Zhuang Chen & Yang-Mei Liu. (2015)
l
-Proline-Catalysed the Synthesis of Aromatic Aldehydes and Ketones and their Acridione Derivatives at Room Temperature
. Journal of Chemical Research 39:8, pages 445-450.
Crossref
Crossref
Fang-Ming Wang, Dan Bao, Bing-Xiang Hu, Ze-Yu Zhou, Deng-Deng Huang, Li-Zhuang Chen & Yuan-Yuan Dan. (2015) Synthesis of 10-Substituted 3,6-Diphenyl-9-Aryl-3,4,6,7,9,10-Hexahydroacridine-1,8(2H,5H)-Dione Derivatives. Journal of Chemical Research 39:7, pages 376-379.
Crossref
Crossref
Chunmei Gao, Wei Zhang, Shengnan He, Shangfu Li, Feng Liu & Yuyang Jiang. (2015) Synthesis and antiproliferative activity of 2,7-diamino l0-(3,5-dimethoxy)benzyl-9(10H)-acridone derivatives as potent telomeric G-quadruplex DNA ligands. Bioorganic Chemistry 60, pages 30-36.
Crossref
Crossref
Xi Li, Chunmei Gao, Ti Yang, Bin Zhang, Chunyan Tan, Hongxia Liu & Yuyang Jiang. (2015)
A POCl
3
-mediated synthesis of substituted fused azoacridones derivatives
. RSC Advances 5:36, pages 28670-28678.
Crossref
Crossref
Jie Zhang, Yali Chen, Xuanming Chen, Xiaoxing Zheng, Weiguo Cao, Jie Chen & Min Zhang. (2014) Synthesis and characterization of oxadisilole-fused acridines, dioxatrisilole-fused acridines and benzo[b]acridines. Tetrahedron 70:35, pages 5820-5827.
Crossref
Crossref
Artur Sikorski & Damian Trzybiński. (2014) Synthesis and structural characterization of a cocrystal salt containing acriflavine and 3,5-dinitrobenzoic acid. Tetrahedron Letters 55:14, pages 2253-2255.
Crossref
Crossref
Xuliang Lang, Lulu Li, Yuzong Chen, Qinsheng Sun, Qin Wu, Feng Liu, Chunyan Tan, Hongxia Liu, Chunmei Gao & Yuyang Jiang. (2013) Novel synthetic acridine derivatives as potent DNA-binding and apoptosis-inducing antitumor agents. Bioorganic & Medicinal Chemistry 21:14, pages 4170-4177.
Crossref
Crossref
Stefano Puccioni, Carla Bazzicalupi, Andrea Bencini, Claudia Giorgi, Barbara Valtancoli, Greta De Filippo, Vito Lippolis, Pier Remigio Salvi, Giangaetano Pietraperzia, Riccardo Chelli & Cristina Gellini. (2013) Tuning the Emission Properties of Fluorescent Ligands by Changing pH: The Unusual Case of an Acridine-Containing Polyamine Macrocycle. The Journal of Physical Chemistry A 117:18, pages 3798-3808.
Crossref
Crossref
Natalia Busto, Begoña García, José M. Leal, Jorge F. Gaspar, Célia Martins, Alessia Boggioni & Fernando Secco. (2011) ACMA (9-amino-6-chloro-2-methoxy acridine) forms three complexes in the presence of DNA. Physical Chemistry Chemical Physics 13:43, pages 19534.
Crossref
Crossref