Journey of anthraquinones as anticancer agents–a systematic review of recent literature

MS Malik, RI Alsantali, RS Jassas, AA Alsimaree… - RSC …, 2021 - pubs.rsc.org
Anthraquinones are privileged chemical scaffolds that have been used for centuries in
various therapeutic applications. The anthraquinone moiety forms the core of various …

Synthesis of quinones with highlighted biological applications: A critical update on the strategies towards bioactive compounds with emphasis on lapachones

EN da Silva Júnior, GAM Jardim, C Jacob… - European Journal of …, 2019 - Elsevier
Naphthoquinones are of key importance in organic synthesis and medicinal chemistry. In the
last few years, various synthetic routes have been developed to prepare bioactive …

Synthesis and antitumor activity of selenium-containing quinone-based triazoles possessing two redox centres, and their mechanistic insights

EHG Da Cruz, MA Silvers, GAM Jardim… - European journal of …, 2016 - Elsevier
Abstract Selenium-containing quinone-based 1, 2, 3-triazoles were synthesized using click
chemistry, the copper catalyzed azide-alkyne 1, 3-dipolar cycloaddition, and evaluated …

New family of antimicrobial agents derived from 1, 4-naphthoquinone

M Janeczko, OM Demchuk, D Strzelecka… - European journal of …, 2016 - Elsevier
Abstract Naphthalene-1, 4-dione derivatives were synthesized and tested against selected
bacterial strains. All the tested compounds were prepared by direct introduction of …

Trypanothione reductase and superoxide dismutase as current drug targets for Trypanosoma cruzi: an overview of compounds with activity against Chagas disease

I Beltran-Hortelano, S Perez-Silanes… - Current Medicinal …, 2017 - ingentaconnect.com
It has been over a century since Carlos Chagas discovered the Trypanosoma cruzi (T. cruzi)
as the causative agent of Chagas disease (CD), a neglected tropical disease with several …

Pioneering 4,11-Dioxo-4,11-dihydro-1H-anthra[2,3-d]imidazol-3-ium Compounds as Promising Survivin Inhibitors by Targeting ILF3/NF110 for Cancer Therapy

J Yuan, Z Liu, Y Dong, F Gao, X Xia… - Journal of Medicinal …, 2023 - ACS Publications
Survivin is a novel attractive target for cancer therapy; however, it is considered undruggable
because it lacks enzymatic activities. Herein, we describe our efforts toward the discovery of …

Overcoming naphthoquinone deactivation: Rhodium-catalyzed C-5 selective C–H iodination as a gateway to functionalized derivatives

GAM Jardim, EN da Silva Júnior, JF Bower - Chemical Science, 2016 - pubs.rsc.org
We report a Rh-catalyzed method for the C-5 selective C–H iodination of naphthoquinones
and show that complementary C-2 selective processes can be achieved under related …

Quinonoid compounds via reactions of lawsone and 2-aminonaphthoquinone with α-bromonitroalkenes and nitroallylic acetates: Structural diversity by C-ring …

TV Baiju, RG Almeida, ST Sivanandan… - European Journal of …, 2018 - Elsevier
Abstract Morita-Baylis-Hillman acetates and α-bromonitroalkenes have been employed in
cascade reactions with lawsone and 2-aminonaphthoquinone for the one-pot synthesis of …

Molecular hybridization as a powerful tool towards multitarget quinoidal systems: Synthesis, trypanocidal and antitumor activities of naphthoquinone-based 5-iodo-1, 4 …

SBBB Bahia, WJ Reis, GAM Jardim, FT Souto… - …, 2016 - pubs.rsc.org
Quinonoid compounds based on 5-iodo-1, 4-disubstituted-, 1, 4-and 1, 5-disubstituted-1, 2,
3-triazoles were synthesized using simple methodologies and evaluated against T. cruzi, the …

Bifunctional naphthoquinone aromatic amide-oxime derivatives exert combined immunotherapeutic and antitumor effects through simultaneous targeting of …

R Huang, X Jing, X Huang, Y Pan, Y Fang… - Journal of medicinal …, 2020 - ACS Publications
Indoleamine-2, 3-dioxygenase 1 (IDO1) and signal transducer and activator of transcription
3 (STAT3) are important targets in the tumor microenvironment for cancer therapy. In the …