Literature DB >> 21602588

Natural and synthetic acridines/acridones as antitumor agents: their biological activities and methods of synthesis.

Grzegorz Cholewiński1, Krystyna Dzierzbicka, Aleksander M Kołodziejczyk.   

Abstract

Acridine derivatives constitute a class of compounds that are being intensively studied as potential anticancer drugs. Acridines are well-known for their high cytotoxic activity; however, their clinical application is limited or even excluded because of side effects. Numerous synthetic methods are focused on the preparation of target acridine skeletons or modifications of naturally occurring compounds, such as acridone alkaloids, that exhibit promising anticancer activities. They have been examined in vitro and in vivo to test their importance for cancer treatment and to establish the mechanism of action at both the molecular and cellular level, which is necessary for the optimization of their properties so that they are suitable in chemotherapy. In this article, we review natural and synthetic acridine/acridone analogs, their application as anticancer drugs and methods for their preparation.

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Year:  2011        PMID: 21602588     DOI: 10.1016/s1734-1140(11)70499-6

Source DB:  PubMed          Journal:  Pharmacol Rep        ISSN: 1734-1140            Impact factor:   3.024


  13 in total

1.  Design, synthesis, in vitro cytotoxic activity evaluation, and apoptosis-induction study of new 9(10H)-acridinone-1,2,3-triazoles.

Authors:  Maryam Mohammadi-Khanaposhtani; Maliheh Safavi; Reyhaneh Sabourian; Mohammad Mahdavi; Mahboobeh Pordeli; Mina Saeedi; Sussan Kabudanian Ardestani; Alireza Foroumadi; Abbas Shafiee; Tahmineh Akbarzadeh
Journal:  Mol Divers       Date:  2015-07-14       Impact factor: 2.943

2.  Acridone suppresses the proliferation of human breast cancer cells in vitro via ATP-binding cassette subfamily G member 2.

Authors:  Licheng Xu; Shuyan Li; Zhi Liang; Haixia Lin; Rongzhan Fu
Journal:  Oncol Lett       Date:  2017-12-11       Impact factor: 2.967

3.  Facile synthesis of unsymmetrical acridines and phenazines by a Rh(III)-catalyzed amination/cyclization/aromatization cascade.

Authors:  Yajing Lian; Joshua R Hummel; Robert G Bergman; Jonathan A Ellman
Journal:  J Am Chem Soc       Date:  2013-08-19       Impact factor: 15.419

4.  Crystal structure and Hirshfeld surface analysis of ethyl 2-[9-(2-hy-droxy-phen-yl)-3,3,6,6-tetra-methyl-1,8-dioxo-2,3,4,4a,5,6,7,8a,9,9a,10,10a-dodeca-hydro-acridin-10-yl]acetate.

Authors:  Omyma A A Abd Allah; Manpreet Kaur; Mehmet Akkurt; Shaaban K Mohamed; Jerry P Jasinski; Sahar M I Elgarhy
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2021-02-12

Review 5.  Medicinal chemistry of acridine and its analogues.

Authors:  Parteek Prasher; Mousmee Sharma
Journal:  Medchemcomm       Date:  2018-08-14       Impact factor: 3.597

6.  Study of Imidazolium Salt Derivatives as PIK3CA Inhibitors Using a Comprehensive in Silico Method.

Authors:  Ming-Yang Wang; Jing-Wei Liang; Xin-Yang Li; Kamara Mohamed Olounfeh; Shi-Long Li; Shan Wang; Lin Wang; Fan-Hao Meng
Journal:  Int J Mol Sci       Date:  2018-03-18       Impact factor: 5.923

7.  Determination of Structural Requirements of N-Substituted Tetrahydro-β-Carboline Imidazolium Salt Derivatives Using in Silico Approaches for Designing MEK-1 Inhibitors.

Authors:  Jingwei Liang; Mingyang Wang; Xinyang Li; Xin He; Chong Cao; Fanhao Meng
Journal:  Molecules       Date:  2017-06-19       Impact factor: 4.411

Review 8.  Harnessing the untapped potential of nucleotide-binding oligomerization domain ligands for cancer immunotherapy.

Authors:  Sanja Nabergoj; Irena Mlinarič-Raščan; Žiga Jakopin
Journal:  Med Res Rev       Date:  2018-12-13       Impact factor: 12.944

9.  Iodinin (1,6-dihydroxyphenazine 5,10-dioxide) from Streptosporangium sp. induces apoptosis selectively in myeloid leukemia cell lines and patient cells.

Authors:  Lene E Myhren; Gyrid Nygaard; Gro Gausdal; Håvard Sletta; Knut Teigen; Kristin F Degnes; Kolbjørn Zahlsen; Anders Brunsvik; Øystein Bruserud; Stein Ove Døskeland; Frode Selheim; Lars Herfindal
Journal:  Mar Drugs       Date:  2013-01-30       Impact factor: 5.118

10.  Acridone derivative 8a induces oxidative stress-mediated apoptosis in CCRF-CEM leukemia cells: application of metabolomics in mechanistic studies of antitumor agents.

Authors:  Yini Wang; Dan Gao; Zhe Chen; Shangfu Li; Chunmei Gao; Deliang Cao; Feng Liu; Hongxia Liu; Yuyang Jiang
Journal:  PLoS One       Date:  2013-05-07       Impact factor: 3.240

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