A comprehensive review of topoisomerase inhibitors as anticancer agents in the past decade
X Liang, Q Wu, S Luan, Z Yin, C He, L Yin, Y Zou… - European journal of …, 2019 - Elsevier
The topoisomerase enzymes play an important role in DNA metabolism, and searching for
enzyme inhibitors is an important target in the search for new anticancer drugs. Discovery of …
enzyme inhibitors is an important target in the search for new anticancer drugs. Discovery of …
Roles of pyridine and pyrimidine derivatives as privileged scaffolds in anticancer agents
S Prachayasittikul, R Pingaew… - Mini Reviews in …, 2017 - ingentaconnect.com
Background: Cancer has been considered to be a global health concern due to the impact of
disease on the quality of life. The continual increase of cancer cases as well as the …
disease on the quality of life. The continual increase of cancer cases as well as the …
Discovery of novel topoisomerase II inhibitors by medicinal chemistry approaches
W Hu, XS Huang, JF Wu, L Yang… - Journal of Medicinal …, 2018 - ACS Publications
DNA topoisomerase II (topo II) is an important enzyme involved in DNA replication,
recombination, and repair. Despite the popular applications of topo II inhibitors in cancer …
recombination, and repair. Despite the popular applications of topo II inhibitors in cancer …
Design, synthesis and biological evaluation of novel 7-alkylamino substituted benzo [a] phenazin derivatives as dual topoisomerase I/II inhibitors
BL Yao, YW Mai, SB Chen, HT Xie, PF Yao… - European journal of …, 2015 - Elsevier
A novel series of benzo [a] phenazin derivatives bearing alkylamino side chains were
designed, synthesized and evaluated for their topoisomerases inhibitory activity as well as …
designed, synthesized and evaluated for their topoisomerases inhibitory activity as well as …
New trinuclear nickel (II) complexes as potential topoisomerase I/IIα inhibitors: in vitro DNA binding, cleavage and cytotoxicity against human cancer cell lines
Nickel (II) complexes containing p-substitute (–H,–CI,–CH3,–OCH3)
isonitrosoacetophenone-based bis (oxime) ligands were synthesized by metal template …
isonitrosoacetophenone-based bis (oxime) ligands were synthesized by metal template …
Design, synthesis, topoisomerase I & II inhibitory activity, antiproliferative activity, and structure–activity relationship study of pyrazoline derivatives: An ATP-competitive …
A series of pyrazoline derivatives (5) were synthesized in 92–96% yields from chalcones (3)
and hydrazides (4). Subsequently, topo-I and IIα-mediated relaxation and antiproliferative …
and hydrazides (4). Subsequently, topo-I and IIα-mediated relaxation and antiproliferative …
Synthesis and biological evaluation of novel pyrazoline derivatives containing indole skeleton as anti-cancer agents targeting topoisomerase II
Y Song, S Feng, J Feng, J Dong, K Yang, Z Liu… - European journal of …, 2020 - Elsevier
In order to develop potent anticaner agents, a novel series of 3-(1H-indol-3-yl)-2, 3, 3a, 4-
tetrahydrothiochromeno [4, 3-c] pyrazole derivatives were synthesized. Structures of all …
tetrahydrothiochromeno [4, 3-c] pyrazole derivatives were synthesized. Structures of all …
Overview of the New Bioactive Heterocycles as Targeting Topoisomerase Inhibitors Useful Against Colon Cancer
MB Santos… - Anti-Cancer Agents …, 2024 - ingentaconnect.com
Colorectal cancer (CRC) is the third most common cancer globally, with high mortality.
Metastatic CRC is incurable in most cases, and multiple drug therapy can increase patients' …
Metastatic CRC is incurable in most cases, and multiple drug therapy can increase patients' …
New spiro-acridines: DNA interaction, antiproliferative activity and inhibition of human DNA topoisomerases
SMV de Almeida, EA Lafayette, WL Silva… - International journal of …, 2016 - Elsevier
Two new spiro-acridines were synthesized by introducing cyano-N-acylhydrazone between
the acridine and phenyl rings followed by spontaneous cyclization. The final compounds (E) …
the acridine and phenyl rings followed by spontaneous cyclization. The final compounds (E) …
New 3-Cyano-2-substituted pyridines induce apoptosis in MCF 7 breast cancer cells
The synthesis of new 3-cyano-2-substituted pyridines bearing various pharmacophores and
functionalities at position 2 is described. The synthesized compounds were evaluated for …
functionalities at position 2 is described. The synthesized compounds were evaluated for …