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

G Cholewiński, K Dzierzbicka… - Pharmacological Reports, 2011 - Elsevier
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; …

The genetic toxicology of acridines

LR Ferguson, WA Denny - Mutation Research/Reviews in Genetic …, 1991 - Elsevier
Summary 1 lntroducuon 2 Classification and physlcochemlcal properties of acridines 2 1 9-
Anunoacndme and related compounds 2 2 Proflavme and related compounds 2 3 …

Adriamycin and daunomycin induce programmed cell death (apoptosis) in tumour cells

A Skladanowski, J Konopa - Biochemical pharmacology, 1993 - Elsevier
HeLa S 3 cells exposed to Adriamycin® and Daunomycin® for 3 hr at EC 90 and 10× EC 90
concentrations and incubated in drug-free medium demonstrated the characteristics of …

Quantitative structure-activity relationship studies on anticancer drugs

SP Gupta - Chemical reviews, 1994 - ACS Publications
Cancer is one of the most formidable diseases of the world. In fact, if there is any disease
which the mankind is still most afraid of it is cancer. Cancer is not one disease, but a group …

Targeting DNA Topoisomerase II in Antifungal Chemotherapy

K Kondaka, I Gabriel - Molecules, 2022 - mdpi.com
Topoisomerase inhibitors have been in use clinically for the treatment of several diseases
for decades. Although those enzymes are significant molecular targets in antibacterial and …

Amino acid or peptide conjugates of acridine/acridone and quinoline/quinolone-containing drugs. A critical examination of their clinical effectiveness within a twenty …

M Kukowska - European Journal of Pharmaceutical Sciences, 2017 - Elsevier
Abstract Acridines/acridones, quinolines/quinolones (chromophores) and their derivatives
constitute extremely important family of compounds in current medicine. Great significance …

Interstrand DNA crosslinking induced by anthracyclines in tumour cells

A Skladanowski, J Konopa - Biochemical pharmacology, 1994 - Elsevier
Using a new mild method it is shown for two anthracyclines, Adriamycin® and Daunomycin,
that these compounds are able to form DNA crosslinks in HeLa S 3 cells. It was also found …

Hypoxia-selective antitumor agents. 1. Relationships between structure, redox properties and hypoxia-selective cytotoxicity for 4-substituted derivatives of nitracrine

WR Wilson, RF Anderson… - Journal of medicinal …, 1989 - ACS Publications
The nitroacridine derivative 9-[[3-(dimethylamino) propyl] amino]-1-nitroacridine (nitracrine)
is selectively cytotoxic to hypoxic tumor cells in culture. However, the compound undergoes …

Synthesis and antitumor activity of conjugates of muramyldipeptide, normuramyldipeptide, and desmuramylpeptides with acridine/acridone derivatives

K Dzierzbicka, AM Kołodziejczyk… - Journal of medicinal …, 2001 - ACS Publications
The synthesis of two groups (Chart 1, types A and B) of conjugates of MDP
(muramyldipeptide) and nor-MDP (normuramyldipeptide) with acridine/acridone derivatives …

Synthesis and antitumor activity of conjugates of muramyldipeptide or normuramyldipeptide with hydroxyacridine/acridone derivatives

K Dzierzbicka, AM Kołodziejczyk - Journal of medicinal chemistry, 2003 - ACS Publications
A series of MDP (muramyldipeptide) or nor-MDP (normuramyldipeptide) analogues modified
at the C-terminus post of the molecule by a formation of an ester bond between the …