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Journey of anthraquinones as anticancer agents - a systematic review of recent literature.

作者信息

Malik M Shaheer, Alsantali Reem I, Jassas Rabab S, Alsimaree Abdulrahman A, Syed Riyaz, Alsharif Meshari A, Kalpana Kulkarni, Morad Moataz, Althagafi Ismail I, Ahmed Saleh A

机构信息

Department of Chemistry, Faculty of Applied Sciences, Umm Al-Qura University Makkah 21955 Saudi Arabia

Department of Pharmaceutical Chemistry, College of Pharmacy, Taif University P. O. Box 11099 Taif 21944 Saudi Arabia.

出版信息

RSC Adv. 2021 Nov 5;11(57):35806-35827. doi: 10.1039/d1ra05686g. eCollection 2021 Nov 4.


DOI:10.1039/d1ra05686g
PMID:35492773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9043427/
Abstract

Anthraquinones are privileged chemical scaffolds that have been used for centuries in various therapeutic applications. The anthraquinone moiety forms the core of various anticancer agents. However, the emergence of drug-resistant cancers warrants the development of new anticancer agents. The research endeavours towards new anthraquinone-based compounds are increasing rapidly in recent years. They are used as a core chemical template to achieve structural modifications, resulting in the development of new anthraquinone-based compounds as promising anticancer agents. Mechanistically, most of the anthraquinone-based compounds inhibit cancer progression by targeting essential cellular proteins. Herein, we review new anthraquinone analogues that have been developed in recent years as anticancer agents. This includes a systematic review of the recent literature (2005-2021) on anthraquinone-based compounds in cell-based models and key target proteins such as kinases, topoisomerases, telomerases, matrix metalloproteinases and G-quadruplexes involved in the viability of cancer cells. In addition to this, the developments in PEG-based delivery of anthraquinones and the toxicity aspects of anthraquinone derivatives are also discussed. The review dispenses a compact background knowledge to understanding anthraquinones for future research on the expansion of anticancer therapeutics.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/57ca436c8c62/d1ra05686g-p2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/e91558315410/d1ra05686g-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/053eb6c1f7e6/d1ra05686g-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/bc3a82d27535/d1ra05686g-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/1d7ffc4d8f0a/d1ra05686g-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/1e723730fbd2/d1ra05686g-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/c6b6dd1e1dfe/d1ra05686g-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/bfc4a5e5c25b/d1ra05686g-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/7afe2d72d761/d1ra05686g-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/0d67797965de/d1ra05686g-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/d9f5105a6960/d1ra05686g-f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/9aa712083371/d1ra05686g-f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/3ccd77aa9bdf/d1ra05686g-f12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/0f6a90cbe7d4/d1ra05686g-f13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/b11d053ea67c/d1ra05686g-f14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/60604ede58f1/d1ra05686g-p1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/57ca436c8c62/d1ra05686g-p2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/e91558315410/d1ra05686g-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/053eb6c1f7e6/d1ra05686g-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/bc3a82d27535/d1ra05686g-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/1d7ffc4d8f0a/d1ra05686g-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/1e723730fbd2/d1ra05686g-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/c6b6dd1e1dfe/d1ra05686g-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/bfc4a5e5c25b/d1ra05686g-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/7afe2d72d761/d1ra05686g-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/0d67797965de/d1ra05686g-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/d9f5105a6960/d1ra05686g-f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/9aa712083371/d1ra05686g-f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/3ccd77aa9bdf/d1ra05686g-f12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/0f6a90cbe7d4/d1ra05686g-f13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/b11d053ea67c/d1ra05686g-f14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/60604ede58f1/d1ra05686g-p1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0551/9043427/57ca436c8c62/d1ra05686g-p2.jpg

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本文引用的文献

[1]
Emodin - A natural anthraquinone derivative with diverse pharmacological activities.

Phytochemistry. 2021-10

[2]
Binding Studies of Aloe-Active Compounds with G-Quadruplex Sequences.

ACS Omega. 2021-7-9

[3]
Pharmacokinetics of Anthraquinones from Medicinal Plants.

Front Pharmacol. 2021-4-15

[4]
G-quadruplexes: a promising target for cancer therapy.

Mol Cancer. 2021-2-25

[5]
Design, synthesis and antitumour evaluation of novel anthraquinone derivatives.

Bioorg Chem. 2021-2

[6]
Inducing Apoptosis through Upregulation of p53: Structure-Activity Exploration of Anthraquinone Analogs.

Med Chem Res. 2020-7

[7]
Design, Synthesis, Molecular Docking, and Biological Evaluation of New Emodin Anthraquinone Derivatives as Potential Antitumor Substances.

Chem Biodivers. 2020-9

[8]
Amides of pyrrole- and thiophene-fused anthraquinone derivatives: A role of the heterocyclic core in antitumor properties.

Eur J Med Chem. 2020-8-1

[9]
Anthraquinone: a promising scaffold for the discovery and development of therapeutic agents in cancer therapy.

Future Med Chem. 2020-6

[10]
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ChemMedChem. 2020-6-4

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