The search of DNA-intercalators as antitumoral drugs: what it worked and what did not work

R Martinez, L Chacon-Garcia - Current medicinal chemistry, 2005 - ingentaconnect.com
The discovery of new compounds with antitumoral activity has become one of the most
important goals in medicinal chemistry. One interesting group of chemotherapeutic agents …

Natural compounds as anticancer agents targeting DNA topoisomerases

C Kumar Jain, H Kumar Majumder… - Current …, 2017 - ingentaconnect.com
DNA topoisomerases are important cellular enzymes found in almost all types of living cells
(eukaryotic and prokaryotic). These enzymes are essential for various DNA metabolic …

[HTML][HTML] A reliable tool to determine cell viability in complex 3-d culture: the acid phosphatase assay

J Friedrich, W Eder, J Castaneda, M Doss, E Huber… - SLAS Discovery, 2007 - Elsevier
Cell-based assays are more complex than cell-free test systems but still reflect a highly
artificial cellular environment. Incorporation of organotypic 3-dimensional (3-D) culture …

Design, synthesis and high antitumor potential of new unsymmetrical bisacridine derivatives towards human solid tumors, specifically pancreatic cancers and their …

E Paluszkiewicz, B Horowska, B Borowa-Mazgaj… - European Journal of …, 2020 - Elsevier
New promising unsymmetrical bisacridine derivatives (UAs), have been developed. Three
groups including 36 compounds were synthesized by the condensation of 4-nitro or 4 …

Antitumour acridines

M Demeunynck - Expert Opinion on Therapeutic Patents, 2004 - Taylor & Francis
DNA remains one of the main targets in antitumour drug design. Due to their polycyclic
planar structure, acridines interact with DNA by intercalation between base pairs and …

Studying the interaction of pirarubicin with DNA and determining pirarubicin in human urine samples: combining excitation-emission fluorescence matrices with …

HY Zou, HL Wu, Y Zhang, SF Li, JF Nie, HY Fu… - Journal of …, 2009 - Springer
In this paper, UV–vis spectroscopy and fluorescence were combined to study the binding of
Calf thymus DNA (ct-DNA) with the anthacycline antibiotic drug pirarubicin (THP). Ethidium …

Evaluation of the safety of C-1311 (SYMADEX) administered in a phase 1 dose escalation trial as a weekly infusion for 3 consecutive weeks in patients with advanced …

N Isambert, M Campone, E Bourbouloux… - European Journal of …, 2010 - Elsevier
PURPOSE: C-1311 is a member of the novel imidazoacridinone family of anticancer agents.
This phase 1 trial was designed to investigate the safety, tolerability and preliminary anti …

Intercalation of imidazoacridinones to DNA and its relevance to cytotoxic and antitumor activity

J Dzięgielewski, B Ślusarski, A Konitz… - Biochemical …, 2002 - Elsevier
Imidazoacridinones (IA) are a class of antitumor agents which includes C-1311, an
interesting drug in clinical trials. This study investigated the mechanism of IA binding to DNA …

Electroanalytical and spectroscopic procedures for examination of interactions between double stranded DNA and intercalating drugs

AM Nowicka, E Zabost, M Donten, Z Mazerska… - Analytical and …, 2007 - Springer
A method is presented for the electroanalytical characterization of interactions of dsDNA with
a drug, under conditions that both agents are dissolved in the phosphate buffer solution and …

Molecular mechanism of the enzymatic oxidation investigated for imidazoacridinone antitumor drug, C-1311

Z Mazerska, P Sowiński, J Konopa - Biochemical pharmacology, 2003 - Elsevier
The imidazoacridinone derivative, C-1311, is an antitumor agent that has been under phase
I of clinical trial. The work presented here aims to elucidate the molecular mechanism of the …