Differential inhibition of cyclic AMP-dependent protein kinase, myosin light chain kinase and protein kinase C by azaacridine and acridine derivatives

Q Chen, LW Deady, GM Polya - 1994 - degruyter.com
A series of 72 acridine and azaacridinie derivatives have been tested as inhibitors of Ca2"-
and phospholipid-activated protein kinase C (PK (C), the catalytic subunit of cyclic AMP …

[HTML][HTML] Novel tetrahydroacridine derivatives with iodobenzoic moieties induce G0/G1 cell cycle arrest and apoptosis in A549 non-small lung cancer and HT-29 …

M Girek, K Kłosiński, B Grobelski, S Pizzimenti… - Molecular and Cellular …, 2019 - Springer
A series of nine tetrahydroacridine derivatives with iodobenzoic moiety were synthesized
and evaluated for their cytotoxic activity against cancer cell lines—A549 (human lung …

Niche for acridine derivatives in anticancer therapy

MR Galdino-Pitta, MGR Pitta, MCA Lima… - Mini Rev Med …, 2013 - ingentaconnect.com
During the last 4 decades, intensive research has focussed on the effect of small organic
molecules with antitumour activity that are able to intercalate into DNA and inhibit …

Synthesis, biological evaluation and virtual screening of some acridone derivatives as potential anticancer agents

AS Oyedele, DN Bogan, CO Okoro - Bioorganic & Medicinal Chemistry, 2020 - Elsevier
Eleven novel acridone derivatives were synthesized and evaluated for their anticancer
activity against 60 human cancer cell lines. Five compounds 8b, 8d, 8g, 8h, and 8k …

Abstract 1923 Anti-Cancer Activity of Acridine Derivatives in Lung and Prostate Cancer Cells

D Williams, J Kocerha, K Aiken, AM Seymour… - Journal of Biological …, 2024 - ASBMB
Acridine compounds consist of a base structure similar to anthracene but with one of the
central carbon-hydrogen groups replaced by Nitrogen and are being widely researched as …

Structural tuning of acridones for developing anticancer agents targeting dihydrofolate reductase

H Singh, M Kaur, H Kaur, I Sharma, A Bhandari… - Bioorganic & Medicinal …, 2019 - Elsevier
Targeting dihydrofolate reductase, here, we report the tumor growth inhibitory activity of
substituted acridones. The screening of the molecules over 60 cell line panel of human …

[PDF][PDF] Rita Ghosh, Sudipta Bhowmik &

D Guha - academia.edu
Several acridine derivatives have been screened for their therapeutic potential and some
are already established as antiprotozoan, antibacterial or anticancer agents. However …

Subcellular localization of proflavine derivative and induction of oxidative stress—In vitro studies

Z Ipóthová, H Paulíková, L Čižeková… - Bioorganic & medicinal …, 2013 - Elsevier
Acridines have been studied for several decades because of their numerous biological
effects, especially anticancer activity. Recently, cytotoxicity of novel acridine derivatives, 3, 6 …

Novel tetrahydroacridine and cyclopentaquinoline derivatives with fluorobenzoic acid moiety induce cell cycle arrest and apoptosis in lung cancer cells by activation of …

P Szymański, P Olszewska, E Mikiciuk-Olasik… - Tumor …, 2017 - journals.sagepub.com
Lung cancer is still the leading cause of cancer-related death worldwide, indicating a
necessity to develop more effective therapy. Acridine derivatives are potential anticancer …

Derives de tetrahydrocyclopenta° c! acridines inhibiteurs de kinases et leurs applications biologiques

PO Belmont, L Meijer, P Cohen, A Patin… - FR Patent App …, 2010 - Google Patents
FR2926550B1 - Derives de tetrahydrocyclopentac!acridines inhibiteurs de kinases et leurs
applications biologiques - Google Patents FR2926550B1 - Derives de …